Pittenger MF, Mackay AM, Beck SC, Jaiswal RK, Douglas R, Mosca JD, Moorman MA, Simonetti DW, Craig S, Marshak DR (1999) Multilineage potential of adult human mesenchymal stem cells. Science 284(5411):143–147
Article
CAS
PubMed
Google Scholar
Jiang Y, Jahagirdar BN, Reinhardt RL, Schwartz RE, Keene CD, Ortiz-Gonzalez XR, Reyes M, Lenvik T, Lund T, Blackstad M, Du J, Aldrich S, Lisberg A, Low WC, Largaespada DA, Verfaillie CM (2002) Pluripotency of mesenchymal stem cells derived from adult marrow. Nature 418(6893):41–49. https://doi.org/10.1038/nature00870
Article
CAS
PubMed
Google Scholar
Wagers AJ, Weissman IL (2004) Plast Adult Stem Cells. Cell 116(5):639–648
Article
CAS
PubMed
Google Scholar
Chen Q, Shou P, Zheng C, Jiang M, Cao G, Yang Q, Cao J, Xie N, Velletri T, Zhang X, Xu C, Zhang L, Yang H, Hou J, Wang Y, Shi Y (2016) Fate decision of mesenchymal stem cells: adipocytes or osteoblasts? Cell Death Differ 23(7):1128–1139. https://doi.org/10.1038/cdd.2015.168
Article
CAS
PubMed
PubMed Central
Google Scholar
Augello A, De Bari C (2010) The regulation of differentiation in mesenchymal stem cells. Hum Gene Ther 21(10):1226–1238. https://doi.org/10.1089/hum.2010.173
Article
CAS
PubMed
Google Scholar
Chijimatsu R, Kobayashi M, Ebina K, Iwahashi T, Okuno Y, Hirao M, Fukuhara A, Nakamura N, Yoshikawa H (2018) Impact of dexamethasone concentration on cartilage tissue formation from human synovial derived stem cells in vitro. Cytotechnology 70(2):819–829. https://doi.org/10.1007/s10616-018-0191-y
Article
CAS
PubMed
PubMed Central
Google Scholar
Kirton JP, Crofts NJ, George SJ, Brennan K, Canfield AE (2007) Wnt/beta-catenin signaling stimulates chondrogenic and inhibits adipogenic differentiation of pericytes: potential relevance to vascular disease? Circ Res 101(6):581–589. https://doi.org/10.1161/CIRCRESAHA.107.156372
Article
CAS
PubMed
Google Scholar
Enomoto H, Furuichi T, Zanma A, Yamana K, Yoshida C, Sumitani S, Yamamoto H, Enomoto-Iwamoto M, Iwamoto M, Komori T (2004) Runx2 deficiency in chondrocytes causes adipogenic changes in vitro. J Cell Sci 117(Pt 3):417–425. https://doi.org/10.1242/jcs.00866
CAS
Article
PubMed
Google Scholar
Qu P, Wang L, Min Y, McKennett L, Keller JR, Lin PC (2016) Vav1 regulates mesenchymal stem cell differentiation decision between adipocyte and chondrocyte via sirt1. Stem Cells 34(7):1934–1946. https://doi.org/10.1002/stem.2365
Article
CAS
PubMed
PubMed Central
Google Scholar
Wang Y, Sul HS (2009) Pref-1 regulates mesenchymal cell commitment and differentiation through Sox9. Cell Metab 9(3):287–302. https://doi.org/10.1016/j.cmet.2009.01.013
Article
CAS
PubMed
PubMed Central
Google Scholar
Okazaki K, Li J, Yu H, Fukui N, Sandell LJ (2002) CCAAT/enhancer-binding proteins beta and delta mediate the repression of gene transcription of cartilage-derived retinoic acid-sensitive protein induced by interleukin-1 beta. J Biol Chem 277(35):31526–31533. https://doi.org/10.1074/jbc.M202815200
Article
CAS
PubMed
Google Scholar
Okuma T, Hirata M, Yano F, Mori D, Kawaguchi H, Chung UI, Tanaka S, Saito T (2015) Regulation of mouse chondrocyte differentiation by CCAAT/enhancer-binding proteins. Biomed Res 36(1):21–29. https://doi.org/10.2220/biomedres.36.21
Article
CAS
PubMed
Google Scholar
Ushijima T, Okazaki K, Tsushima H, Iwamoto Y (2014) CCAAT/enhancer-binding protein beta regulates the repression of type II collagen expression during the differentiation from proliferative to hypertrophic chondrocytes. J Biol Chem 289(5):2852–2863. https://doi.org/10.1074/jbc.M113.492843
Article
CAS
PubMed
Google Scholar
Stockl S, Bauer RJ, Bosserhoff AK, Gottl C, Grifka J, Grassel S (2013) Sox9 modulates cell survival and adipogenic differentiation of multipotent adult rat mesenchymal stem cells. J Cell Sci 126(Pt 13):2890–2902. https://doi.org/10.1242/jcs.124305
Article
CAS
PubMed
Google Scholar
Ushita M, Saito T, Ikeda T, Yano F, Higashikawa A, Ogata N, Chung U, Nakamura K, Kawaguchi H (2009) Transcriptional induction of SOX9 by NF-kappaB family member RelA in chondrogenic cells. Osteoarthr Cartil 17(8):1065–1075. https://doi.org/10.1016/j.joca.2009.02.003
Article
CAS
Google Scholar
Ikeda T, Kamekura S, Mabuchi A, Kou I, Seki S, Takato T, Nakamura K, Kawaguchi H, Ikegawa S, Chung UI (2004) The combination of SOX5, SOX6, and SOX9 (the SOX trio) provides signals sufficient for induction of permanent cartilage. Arthritis Rheum 50(11):3561–3573. https://doi.org/10.1002/art.20611
Article
CAS
PubMed
Google Scholar
Chen S, Fu P, Wu H, Pei M (2017) Meniscus, articular cartilage and nucleus pulposus: a comparative review of cartilage-like tissues in anatomy, development and function. Cell Tissue Res 5:6. https://doi.org/10.1007/s00441-017-2613-0
Article
Google Scholar
Bhattacharjee M, Coburn J, Centola M, Murab S, Barbero A, Kaplan DL, Martin I, Ghosh S (2015) Tissue engineering strategies to study cartilage development, degeneration and regeneration. Adv Drug Deliv Rev 84:107–122. https://doi.org/10.1016/j.addr.2014.08.010
Article
CAS
PubMed
Google Scholar
Mikic B, Johnson TL, Chhabra AB, Schalet BJ, Wong M, Hunziker EB (2000) Differential effects of embryonic immobilization on the development of fibrocartilaginous skeletal elements. J Rehabil Res Dev 37(2):127–133
CAS
PubMed
Google Scholar
Storm EE, Kingsley DM (1996) Joint patterning defects caused by single and double mutations in members of the bone morphogenetic protein (BMP) family. Development 122(12):3969–3979
CAS
PubMed
Google Scholar
Decker RS (2017) Articular cartilage and joint development from embryogenesis to adulthood. Semin Cell Dev Biol 62:50–56. https://doi.org/10.1016/j.semcdb.2016.10.005
Article
PubMed
Google Scholar
Seale P, Kajimura S, Yang W, Chin S, Rohas LM, Uldry M, Tavernier G, Langin D, Spiegelman BM (2007) Transcriptional control of brown fat determination by PRDM16. Cell Metab 6(1):38–54. https://doi.org/10.1016/j.cmet.2007.06.001
Article
CAS
PubMed
PubMed Central
Google Scholar
Seale P, Bjork B, Yang W, Kajimura S, Chin S, Kuang S, Scime A, Devarakonda S, Conroe HM, Erdjument-Bromage H, Tempst P, Rudnicki MA, Beier DR, Spiegelman BM (2008) PRDM16 controls a brown fat/skeletal muscle switch. Nature 454(7207):961–967. https://doi.org/10.1038/nature07182
Article
CAS
PubMed
PubMed Central
Google Scholar
Sanchez-Gurmaches J, Hung CM, Sparks CA, Tang Y, Li H, Guertin DA (2012) PTEN loss in the Myf5 lineage redistributes body fat and reveals subsets of white adipocytes that arise from Myf5 precursors. Cell Metab 16(3):348–362. https://doi.org/10.1016/j.cmet.2012.08.003
Article
CAS
PubMed
PubMed Central
Google Scholar
Billon N, Iannarelli P, Monteiro MC, Glavieux-Pardanaud C, Richardson WD, Kessaris N, Dani C, Dupin E (2007) The generation of adipocytes by the neural crest. Development 134(12):2283–2292. https://doi.org/10.1242/dev.002642
Article
CAS
PubMed
Google Scholar
Gesta S, Tseng YH, Kahn CR (2007) Developmental origin of fat: tracking obesity to its source. Cell 131(2):242–256. https://doi.org/10.1016/j.cell.2007.10.004
Article
CAS
PubMed
Google Scholar
Rosen ED, MacDougald OA (2006) Adipocyte differentiation from the inside out. Nat Rev Mol Cell Biol 7(12):885–896. https://doi.org/10.1038/nrm2066
Article
CAS
PubMed
Google Scholar
Linhart HG, Ishimura-Oka K, DeMayo F, Kibe T, Repka D, Poindexter B, Bick RJ, Darlington GJ (2001) C/EBPalpha is required for differentiation of white, but not brown, adipose tissue. Proc Natl Acad Sci USA 98(22):12532–12537. https://doi.org/10.1073/pnas.211416898
Article
CAS
PubMed
PubMed Central
Google Scholar
Schulz TJ, Tseng YH (2009) Emerging role of bone morphogenetic proteins in adipogenesis and energy metabolism. Cytokine Growth Factor Rev 20(5–6):523–531. https://doi.org/10.1016/j.cytogfr.2009.10.019
Article
CAS
PubMed
PubMed Central
Google Scholar
Iwasaki M, Nakata K, Nakahara H, Nakase T, Kimura T, Kimata K, Caplan AI, Ono K (1993) Transforming growth factor-beta 1 stimulates chondrogenesis and inhibits osteogenesis in high density culture of periosteum-derived cells. Endocrinology 132(4):1603–1608. https://doi.org/10.1210/endo.132.4.8462458
Article
CAS
PubMed
Google Scholar
Erickson GR, Gimble JM, Franklin DM, Rice HE, Awad H, Guilak F (2002) Chondrogenic potential of adipose tissue-derived stromal cells in vitro and in vivo. Biochem Biophys Res Commun 290(2):763–769. https://doi.org/10.1006/bbrc.2001.6270
Article
CAS
PubMed
Google Scholar
Barry F, Boynton RE, Liu B, Murphy JM (2001) Chondrogenic differentiation of mesenchymal stem cells from bone marrow: differentiation-dependent gene expression of matrix components. Exp Cell Res 268(2):189–200. https://doi.org/10.1006/excr.2001.5278
Article
CAS
PubMed
Google Scholar
Awad HA, Halvorsen YD, Gimble JM, Guilak F (2003) Effects of transforming growth factor beta1 and dexamethasone on the growth and chondrogenic differentiation of adipose-derived stromal cells. Tissue Eng 9(6):1301–1312. https://doi.org/10.1089/10763270360728215
Article
CAS
PubMed
Google Scholar
Handorf AM, Chamberlain CS, Li WJ (2015) Endogenously produced Indian Hedgehog regulates TGFbeta-driven chondrogenesis of human bone marrow stromal/stem cells. Stem Cells Dev 24(8):995–1007. https://doi.org/10.1089/scd.2014.0266
Article
CAS
PubMed
Google Scholar
Yoo JU, Barthel TS, Nishimura K, Solchaga L, Caplan AI, Goldberg VM, Johnstone B (1998) The chondrogenic potential of human bone-marrow-derived mesenchymal progenitor cells. J Bone Joint Surg Am 80(12):1745–1757
Article
CAS
PubMed
Google Scholar
Kitamura H (2004) Establishment of a bipotent cell line CL-1 which differentiates into chondrocytes and adipocytes from adult mouse. Osteoarthr Cartil 12(1):25–37
Article
Google Scholar
Zhou S, Eid K, Glowacki J (2004) Cooperation between TGF-beta and Wnt pathways during chondrocyte and adipocyte differentiation of human marrow stromal cells. J Bone Miner Res 19(3):463–470. https://doi.org/10.1359/JBMR.0301239
Article
CAS
PubMed
Google Scholar
Ignotz RA, Massague J (1985) Type beta transforming growth factor controls the adipogenic differentiation of 3T3 fibroblasts. Proc Natl Acad Sci USA 82(24):8530–8534
Article
CAS
PubMed
PubMed Central
Google Scholar
Tsurutani Y, Fujimoto M, Takemoto M, Irisuna H, Koshizaka M, Onishi S, Ishikawa T, Mezawa M, He P, Honjo S, Maezawa Y, Saito Y, Yokote K (2011) The roles of transforming growth factor-beta and Smad3 signaling in adipocyte differentiation and obesity. Biochem Biophys Res Commun 407(1):68–73. https://doi.org/10.1016/j.bbrc.2011.02.106
Article
CAS
PubMed
Google Scholar
Coricor G, Serra R (2016) TGF-beta regulates phosphorylation and stabilization of Sox9 protein in chondrocytes through p38 and Smad dependent mechanisms. Sci Rep 6:38616. https://doi.org/10.1038/srep38616
Article
CAS
PubMed
PubMed Central
Google Scholar
Tuli R, Seghatoleslami MR, Tuli S, Howard MS, Danielson KG, Tuan RS (2002) p38 MAP kinase regulation of AP-2 binding in TGF-beta1-stimulated chondrogenesis of human trabecular bone-derived cells. Ann N Y Acad Sci 961:172–177
Article
CAS
PubMed
Google Scholar
Kim BS, Kang KS, Kang SK (2010) Soluble factors from ASCs effectively direct control of chondrogenic fate. Cell Prolif 43(3):249–261. https://doi.org/10.1111/j.1365-2184.2010.00680.x
Article
CAS
PubMed
Google Scholar
Li J, Zhao Z, Liu J, Huang N, Long D, Wang J, Li X, Liu Y (2010) MEK/ERK and p38 MAPK regulate chondrogenesis of rat bone marrow mesenchymal stem cells through delicate interaction with TGF-beta1/Smads pathway. Cell Prolif 43(4):333–343. https://doi.org/10.1111/j.1365-2184.2010.00682.x
Article
CAS
PubMed
PubMed Central
Google Scholar
Choy L, Skillington J, Derynck R (2000) Roles of autocrine TGF-beta receptor and Smad signaling in adipocyte differentiation. J Cell Biol 149(3):667–682
Article
CAS
PubMed
PubMed Central
Google Scholar
Choy L, Derynck R (2003) Transforming growth factor-beta inhibits adipocyte differentiation by Smad3 interacting with CCAAT/enhancer-binding protein (C/EBP) and repressing C/EBP transactivation function. J Biol Chem 278(11):9609–9619. https://doi.org/10.1074/jbc.M212259200
Article
CAS
PubMed
Google Scholar
Sekiya I, Larson BL, Vuoristo JT, Reger RL, Prockop DJ (2005) Comparison of effect of BMP-2, -4, and -6 on in vitro cartilage formation of human adult stem cells from bone marrow stroma. Cell Tissue Res 320(2):269–276. https://doi.org/10.1007/s00441-004-1075-3
Article
CAS
PubMed
Google Scholar
Sottile V, Seuwen K (2000) Bone morphogenetic protein-2 stimulates adipogenic differentiation of mesenchymal precursor cells in synergy with BRL 49653 (rosiglitazone). FEBS Lett 475(3):201–204
Article
CAS
PubMed
Google Scholar
Wang EA, Israel DI, Kelly S, Luxenberg DP (1993) Bone morphogenetic protein-2 causes commitment and differentiation in C3H10T1/2 and 3T3 cells. Growth Factors 9(1):57–71
Article
CAS
PubMed
Google Scholar
Schmitt B, Ringe J, Haupl T, Notter M, Manz R, Burmester GR, Sittinger M, Kaps C (2003) BMP2 initiates chondrogenic lineage development of adult human mesenchymal stem cells in high-density culture. Res Biol Divers 71(9–10):567–577. https://doi.org/10.1111/j.1432-0436.2003.07109003.x
CAS
Article
Google Scholar
Kuroda R, Usas A, Kubo S, Corsi K, Peng HR, Rose T, Cummins J, Fu FH, Huard J (2006) Cartilage repair using bone morphogenetic protein 4 and muscle-derived stem cells. Arthritis Rheum 54(2):433–442. https://doi.org/10.1002/art.21632
Article
CAS
PubMed
Google Scholar
Steinert A, Weber M, Dimmler A, Julius C, Schutze N, Noth U, Cramer H, Eulert J, Zimmermann U, Hendrich C (2003) Chondrogenic differentiation of mesenchymal progenitor cells encapsulated in ultrahigh-viscosity alginate. J Orthopaed Res 21(6):1090–1097. https://doi.org/10.1016/S0736-0266(03)00100-1
Article
CAS
Google Scholar
Semba I, Nonaka K, Takahashi I, Takahashi K, Dashner R, Shum L, Nuckolls GH, Slavkin HC (2000) Positionally-dependent chondrogenesis induced by BMP4 is co-regulated by Sox9 and Msx2. Dev Dynam 217(4):401–414. https://doi.org/10.1002/(Sici)1097-0177(200004)217:4%3c401:Aid-Dvdy7%3e3.0.Co;2-D
Article
CAS
Google Scholar
Nakayama N, Duryea D, Manoukian R, Chow G, Han CYE (2003) Macroscopic cartilage formation with embryonic stem-cell-derived mesodermal progenitor cells. J Cell Sci 116(10):2015–2028. https://doi.org/10.1242/jcs.00417
Article
CAS
PubMed
Google Scholar
Taha MF, Valojerdi MR, Mowla SJ (2006) Effect of bone morphogenetic protein-4 (BMP-4) on adipocyte differentiation from mouse embryonic stem cells. Anat Histol Embryol 35(4):271–278. https://doi.org/10.1111/j.1439-0264.2006.00680.x
Article
CAS
PubMed
Google Scholar
Shintani N, Hunziker EB (2007) Chondrogenic differentiation of bovine synovium—bone morphogenetic proteins 2 and 7 and transforming growth factor beta 1 induce the formation of different types of cartilaginous tissue. Arthritis Rheum 56(6):1869–1879. https://doi.org/10.1002/art.22701
Article
CAS
PubMed
Google Scholar
Miyamoto C, Matsumoto T, Sakimura K, Shindo H (2007) Osteogenic protein-1 with transforming growth factor-beta 1: potent inducer of chondrogenesis of synovial mesenchymal stem cells in vitro. J Orthop Sci 12(6):555–561. https://doi.org/10.1007/s00776-007-1176-4
Article
CAS
PubMed
Google Scholar
Brown PT, Squire MW, Li WJ (2014) Characterization and evaluation of mesenchymal stem cells derived from human embryonic stem cells and bone marrow. Cell Tissue Res 358(1):149–164. https://doi.org/10.1007/s00441-014-1926-5
Article
CAS
PubMed
PubMed Central
Google Scholar
Cicione C, Muinos-Lopez E, Hermida-Gomez T, Fuentes-Boquete I, Diaz-Prado S, Blanco FJ (2015) Alternative protocols to induce chondrogenic differentiation: transforming growth factor-beta superfamily. Cell Tissue Bank 16(2):195–207. https://doi.org/10.1007/s10561-014-9472-7
Article
CAS
PubMed
Google Scholar
Lee PT, Li WJ (2017) Chondrogenesis of embryonic stem cell-derived mesenchymal stem cells induced by TGF1 and BMP7 through increased TGF receptor expression and endogenous TGF1 production. J Cell Biochem 118(1):172–181. https://doi.org/10.1002/jcb.25623
Article
CAS
PubMed
Google Scholar
Tseng YH, Kokkotou E, Schulz TJ, Huang TL, Winnay JN, Taniguchi CM, Tran TT, Suzuki R, Espinoza DO, Yamamoto Y, Ahrens MJ, Dudley AT, Norris AW, Kulkarni RN, Kahn CR (2008) New role of bone morphogenetic protein 7 in brown adipogenesis and energy expenditure. Nature 454(7207):1000–1044. https://doi.org/10.1038/nature07221
Article
CAS
PubMed
PubMed Central
Google Scholar
Neumann K, Endres M, Ringe J, Flath B, Manz R, Haupl T, Sittinger M, Kaps C (2007) BMP7 promotes adipogenic but not osteo-/chondrogenic differentiation of adult human bone marrow-derived stem cells in high-density micro-mass culture. J Cell Biochem 102(3):626–637. https://doi.org/10.1002/jcb.21319
Article
CAS
PubMed
Google Scholar
Shen B, Wei A, Whittaker S, Williams LA, Tao H, Ma DD, Diwan AD (2010) The role of BMP-7 in chondrogenic and osteogenic differentiation of human bone marrow multipotent mesenchymal stromal cells in vitro. J Cell Biochem 109(2):406–416. https://doi.org/10.1002/jcb.22412
CAS
Article
PubMed
Google Scholar
Spinella-Jaegle S, Rawadi G, Kawai S, Gallea S, Faucheu C, Mollat P, Courtois B, Bergaud B, Ramez V, Blanchet AM, Adelmant G, Baron R, Roman-Roman S (2001) Sonic hedgehog increases the commitment of pluripotent mesenchymal cells into the osteoblastic lineage and abolishes adipocytic differentiation. J Cell Sci 114(Pt 11):2085–2094
CAS
PubMed
Google Scholar
Fontaine C, Cousin W, Plaisant M, Dani C, Peraldi P (2008) Hedgehog signaling alters adipocyte maturation of human mesenchymal stem cells. Stem Cells 26(4):1037–1046. https://doi.org/10.1634/stemcells.2007-0974
Article
CAS
PubMed
Google Scholar
Lanske B, Karaplis AC, Lee K, Luz A, Vortkamp A, Pirro A, Karperien M, Defize LH, Ho C, Mulligan RC, Abou-Samra AB, Juppner H, Segre GV, Kronenberg HM (1996) PTH/PTHrP receptor in early development and Indian hedgehog-regulated bone growth. Science 273(5275):663–666
Article
CAS
PubMed
Google Scholar
St-Jacques B, Hammerschmidt M, McMahon AP (1999) Indian hedgehog signaling regulates proliferation and differentiation of chondrocytes and is essential for bone formation. Genes Dev 13(16):2072–2086
Article
CAS
PubMed
PubMed Central
Google Scholar
Mundy C, Bello A, Sgariglia F, Koyama E, Pacifici M (2016) HhAntag, a hedgehog signaling antagonist, suppresses chondrogenesis and modulates canonical and non-canonical BMP signaling. J Cell Physiol 231(5):1033–1044. https://doi.org/10.1002/jcp.25192
Article
CAS
PubMed
Google Scholar
Enomoto-Iwamoto M, Nakamura T, Aikawa T, Higuchi Y, Yuasa T, Yamaguchi A, Nohno T, Noji S, Matsuya T, Kurisu K, Koyama E, Pacifici M, Iwamoto M (2000) Hedgehog proteins stimulate chondrogenic cell differentiation and cartilage formation. J Bone Miner Res 15(9):1659–1668. https://doi.org/10.1359/jbmr.2000.15.9.1659
Article
CAS
PubMed
Google Scholar
James AW, Leucht P, Levi B, Carre AL, Xu Y, Helms JA, Longaker MT (2010) Sonic Hedgehog influences the balance of osteogenesis and adipogenesis in mouse adipose-derived stromal cells. Tissue Eng Part A 16(8):2605–2616. https://doi.org/10.1089/ten.TEA.2010.0048
Article
CAS
PubMed
PubMed Central
Google Scholar
Suh JM, Gao X, McKay J, McKay R, Salo Z, Graff JM (2006) Hedgehog signaling plays a conserved role in inhibiting fat formation. Cell Metab 3(1):25–34. https://doi.org/10.1016/j.cmet.2005.11.012
Article
CAS
PubMed
Google Scholar
Pospisilik JA, Schramek D, Schnidar H, Cronin SJ, Nehme NT, Zhang X, Knauf C, Cani PD, Aumayr K, Todoric J, Bayer M, Haschemi A, Puviindran V, Tar K, Orthofer M, Neely GG, Dietzl G, Manoukian A, Funovics M, Prager G, Wagner O, Ferrandon D, Aberger F, Hui CC, Esterbauer H, Penninger JM (2010) Drosophila genome-wide obesity screen reveals hedgehog as a determinant of brown versus white adipose cell fate. Cell 140(1):148–160. https://doi.org/10.1016/j.cell.2009.12.027
Article
CAS
PubMed
Google Scholar
Zehentner BK, Leser U, Burtscher H (2000) BMP-2 and sonic hedgehog have contrary effects on adipocyte-like differentiation of C3H10T1/2 cells. DNA Cell Biol 19(5):275–281. https://doi.org/10.1089/10445490050021186
Article
CAS
PubMed
Google Scholar
Kim W, Kim M, Jho EH (2013) Wnt/beta-catenin signalling: from plasma membrane to nucleus. Biochem J 450:9–21
Article
CAS
PubMed
Google Scholar
Niehrs C (2012) The complex world of WNT receptor signalling. Nat Rev Mol Cell Biol 13(12):767–779. https://doi.org/10.1038/nrm3470
Article
CAS
PubMed
Google Scholar
Fischer L, Boland G, Tuan RS (2002) Wnt-3A enhances bone morphogenetic protein-2-mediated chondrogenesis of murine C3H10T1/2 mesenchymal cells. J Biol Chem 277(34):30870–30878. https://doi.org/10.1074/jbc.M109330200
Article
CAS
PubMed
Google Scholar
Im GI, Quan Z (2010) The effects of Wnt inhibitors on the chondrogenesis of human mesenchymal stem cells. Tissue Eng Part A 16(7):2405–2413. https://doi.org/10.1089/ten.TEA.2009.0359
Article
CAS
PubMed
Google Scholar
Laudes M (2011) Role of WNT signalling in the determination of human mesenchymal stem cells into preadipocytes. J Mol Endocrinol 46(2):R65–R72. https://doi.org/10.1530/JME-10-0169
CAS
Article
PubMed
Google Scholar
Ross SE, Hemati N, Longo KA, Bennett CN, Lucas PC, Erickson RL, MacDougald OA (2000) Inhibition of adipogenesis by Wnt signaling. Science 289(5481):950–953
Article
CAS
PubMed
Google Scholar
Liu J, Farmer SR (2004) Regulating the balance between peroxisome proliferator-activated receptor gamma and beta-catenin signaling during adipogenesis. A glycogen synthase kinase 3beta phosphorylation-defective mutant of beta-catenin inhibits expression of a subset of adipogenic genes. J Biol Chem 279(43):45020–45027. https://doi.org/10.1074/jbc.m407050200
Article
CAS
PubMed
Google Scholar
Moldes M, Zuo Y, Morrison RF, Silva D, Park BH, Liu J, Farmer SR (2003) Peroxisome-proliferator-activated receptor gamma suppresses Wnt/beta-catenin signalling during adipogenesis. Biochem J 376(Pt 3):607–613. https://doi.org/10.1042/BJ20030426
Article
CAS
PubMed
PubMed Central
Google Scholar
Cawthorn WP, Bree AJ, Yao Y, Du B, Hemati N, Martinez-Santibanez G, MacDougald OA (2012) Wnt6, Wnt10a and Wnt10b inhibit adipogenesis and stimulate osteoblastogenesis through a beta-catenin-dependent mechanism. Bone 50(2):477–489. https://doi.org/10.1016/j.bone.2011.08.010
Article
CAS
PubMed
Google Scholar
Kawai M, Mushiake S, Bessho K, Murakami M, Namba N, Kokubu C, Michigami T, Ozono K (2007) Wnt/Lrp/beta-catenin signaling suppresses adipogenesis by inhibiting mutual activation of PPARgamma and C/EBPalpha. Biochem Biophys Res Commun 363(2):276–282. https://doi.org/10.1016/j.bbrc.2007.08.088
Article
CAS
PubMed
Google Scholar
Park JR, Jung JW, Lee YS, Kang KS (2008) The roles of Wnt antagonists Dkk1 and sFRP4 during adipogenesis of human adipose tissue-derived mesenchymal stem cells. Cell Prolif 41(6):859–874. https://doi.org/10.1111/j.1365-2184.2008.00565.x
Article
CAS
PubMed
Google Scholar
Ehrlund A, Mejhert N, Lorente-Cebrian S, Astrom G, Dahlman I, Laurencikiene J, Ryden M (2013) Characterization of the Wnt inhibitors secreted frizzled-related proteins (SFRPs) in human adipose tissue. J Clin Endocrinol Metab 98(3):E503–E508. https://doi.org/10.1210/jc.2012-3416
Article
CAS
PubMed
Google Scholar
Bennett CN, Ross SE, Longo KA, Bajnok L, Hemati N, Johnson KW, Harrison SD, MacDougald OA (2002) Regulation of Wnt signaling during adipogenesis. J Biol Chem 277(34):30998–31004. https://doi.org/10.1074/jbc.M204527200
Article
CAS
PubMed
Google Scholar
Fairfield H, Falank C, Harris E, Demambro V, McDonald M, Pettitt JA, Mohanty ST, Croucher P, Kramer I, Kneissel M, Rosen CJ, Reagan MR (2018) The skeletal cell-derived molecule sclerostin drives bone marrow adipogenesis. J Cell Physiol 233(2):1156–1167. https://doi.org/10.1002/jcp.25976
Article
CAS
PubMed
Google Scholar
Cianferotti L, Demay MB (2007) VDR-mediated inhibition of DKK1 and SFRP2 suppresses adipogenic differentiation of murine bone marrow stromal cells. J Cell Biochem 101(1):80–88. https://doi.org/10.1002/jcb.21151
Article
CAS
PubMed
Google Scholar
Jin EJ, Park JH, Lee SY, Chun JS, Bang OS, Kang SS (2006) Wnt-5a is involved in TGF-beta3-stimulated chondrogenic differentiation of chick wing bud mesenchymal cells. Int J Biochem Cell Biol 38(2):183–195. https://doi.org/10.1016/j.biocel.2005.08.013
Article
CAS
PubMed
Google Scholar
Liu S, Zhang E, Yang M, Lu L (2014) Overexpression of Wnt11 promotes chondrogenic differentiation of bone marrow-derived mesenchymal stem cells in synergism with TGF-beta. Mol Cell Biochem 390(1–2):123–131. https://doi.org/10.1007/s11010-014-1963-0
Article
CAS
PubMed
Google Scholar
Hsu SH, Huang GS (2013) Substrate-dependent Wnt signaling in MSC differentiation within biomaterial-derived 3D spheroids. Biomaterials 34(20):4725–4738. https://doi.org/10.1016/j.biomaterials.2013.03.031
Article
CAS
PubMed
Google Scholar
Zhang Y, Li J, Davis ME, Pei M (2015) Delineation of in vitro chondrogenesis of human synovial stem cells following preconditioning using decellularized matrix. Acta Biomater 20:39–50. https://doi.org/10.1016/j.actbio.2015.04.001
Article
CAS
PubMed
PubMed Central
Google Scholar
Nishizuka M, Koyanagi A, Osada S, Imagawa M (2008) Wnt4 and Wnt5a promote adipocyte differentiation. FEBS Lett 582(21–22):3201–3205. https://doi.org/10.1016/j.febslet.2008.08.011
Article
CAS
PubMed
Google Scholar
Grogan SP, Olee T, Hiraoka K, Lotz MK (2008) Repression of chondrogenesis through binding of notch signaling proteins HES-1 and HEY-1 to N-box domains in the COL2A1 enhancer site. Arthritis Rheum 58(9):2754–2763. https://doi.org/10.1002/art.23730
Article
PubMed
PubMed Central
Google Scholar
Tian Y, Xu Y, Fu Q, Chang M, Wang Y, Shang X, Wan C, Marymont JV, Dong Y (2015) Notch inhibits chondrogenic differentiation of mesenchymal progenitor cells by targeting Twist1. Mol Cell Endocrinol 403:30–38. https://doi.org/10.1016/j.mce.2015.01.015
Article
CAS
PubMed
PubMed Central
Google Scholar
Osathanon T, Subbalekha K, Sastravaha P, Pavasant P (2012) Notch signalling inhibits the adipogenic differentiation of single-cell-derived mesenchymal stem cell clones isolated from human adipose tissue. Cell Biol Int 36(12):1161–1170. https://doi.org/10.1042/CBI20120288
Article
CAS
PubMed
Google Scholar
Lai PY, Tsai CB, Tseng MJ (2013) Active form Notch4 promotes the proliferation and differentiation of 3T3-L1 preadipocytes. Biochem Biophys Res Commun 430(3):1132–1139. https://doi.org/10.1016/j.bbrc.2012.12.024
Article
CAS
PubMed
Google Scholar
Garces C, Ruiz-Hidalgo MJ, Font de Mora J, Park C, Miele L, Goldstein J, Bonvini E, Porras A, Laborda J (1997) Notch-1 controls the expression of fatty acid-activated transcription factors and is required for adipogenesis. J Biol Chem 272(47):29729–29734
Article
CAS
PubMed
Google Scholar
Ross DA, Rao PK, Kadesch T (2004) Dual roles for the Notch target gene Hes-1 in the differentiation of 3T3-L1 preadipocytes. Mol Cell Biol 24(8):3505–3513
Article
CAS
PubMed
PubMed Central
Google Scholar
Ugarte F, Ryser M, Thieme S, Fierro FA, Navratiel K, Bornhauser M, Brenner S (2009) Notch signaling enhances osteogenic differentiation while inhibiting adipogenesis in primary human bone marrow stromal cells. Exp Hematol 37(7):867–875. https://doi.org/10.1016/j.exphem.2009.03.007
Article
CAS
PubMed
Google Scholar
Song BQ, Chi Y, Li X, Du WJ, Han ZB, Tian JJ, Li JJ, Chen F, Wu HH, Han LX, Lu SH, Zheng YZ, Han ZC (2015) Inhibition of notch signaling promotes the adipogenic differentiation of mesenchymal stem cells through autophagy activation and PTEN-PI3K/AKT/mTOR pathway. Cell Physiol Biochem 36(5):1991–2002. https://doi.org/10.1159/000430167
Article
CAS
PubMed
Google Scholar
Ba K, Yang X, Wu L, Wei X, Fu N, Fu Y, Cai X, Yao Y, Ge Y, Lin Y (2012) Jagged-1-mediated activation of notch signalling induces adipogenesis of adipose-derived stem cells. Cell Prolif 45(6):538–544. https://doi.org/10.1111/j.1365-2184.2012.00850.x
Article
CAS
PubMed
PubMed Central
Google Scholar
Li J, Hansen KC, Zhang Y, Dong C, Dinu CZ, Dzieciatkowska M, Pei M (2014) Rejuvenation of chondrogenic potential in a young stem cell microenvironment. Biomaterials 35(2):642–653. https://doi.org/10.1016/j.biomaterials.2013.09.099
Article
CAS
PubMed
Google Scholar
Xiao Y, Peperzak V, van Rijn L, Borst J, de Bruijn JD (2010) Dexamethasone treatment during the expansion phase maintains stemness of bone marrow mesenchymal stem cells. J Tissue Eng Regen Med 4(5):374–386. https://doi.org/10.1002/term.250
Article
CAS
PubMed
Google Scholar
Derfoul A, Perkins GL, Hall DJ, Tuan RS (2006) Glucocorticoids promote chondrogenic differentiation of adult human mesenchymal stem cells by enhancing expression of cartilage extracellular matrix genes. Stem Cells 24(6):1487–1495. https://doi.org/10.1634/stemcells.2005-0415
Article
CAS
PubMed
Google Scholar
Tangtrongsup S, Kisiday JD (2016) Effects of dexamethasone concentration and timing of exposure on chondrogenesis of equine bone marrow-derived mesenchymal stem cells. Cartilage 7(1):92–103. https://doi.org/10.1177/1947603515595263
Article
CAS
PubMed
PubMed Central
Google Scholar
Naito M, Ohashi A, Takahashi T (2015) Dexamethasone inhibits chondrocyte differentiation by suppression of Wnt/beta-catenin signaling in the chondrogenic cell line ATDC5. Histochem Cell Biol 144(3):261–272. https://doi.org/10.1007/s00418-015-1334-2
Article
CAS
PubMed
Google Scholar
Mouw JK, Connelly JT, Wilson CG, Michael KE, Levenston ME (2007) Dynamic compression regulates the expression and synthesis of chondrocyte-specific matrix molecules in bone marrow stromal cells. Stem Cells 25(3):655–663. https://doi.org/10.1634/stemcells.2006-0435
Article
CAS
PubMed
Google Scholar
Kurth T, Hedbom E, Shintani N, Sugimoto M, Chen FH, Haspl M, Martinovic S, Hunziker EB (2007) Chondrogenic potential of human synovial mesenchymal stem cells in alginate. Osteoarthr Cartil 15(10):1178–1189. https://doi.org/10.1016/j.joca.2007.03.015
Article
CAS
Google Scholar
Shintani N, Hunziker EB (2011) Differential effects of dexamethasone on the chondrogenesis of mesenchymal stromal cells influence of microenvironment, tissue origin and growth factor. Eur Cells Mater 22:302–319
Article
CAS
Google Scholar
Oshina H, Sotome S, Yoshii T, Torigoe I, Sugata Y, Maehara H, Marukawa E, Omura K, Shinomiya K (2007) Effects of continuous dexamethasone treatment on differentiation capabilities of bone marrow-derived mesenchymal cells. Bone 41(4):575–583. https://doi.org/10.1016/j.bone.2007.06.022
Article
CAS
PubMed
Google Scholar
Naito M, Omoteyama K, Mikami Y, Takahashi T, Takagi M (2012) Inhibition of Wnt/beta-catenin signaling by dexamethasone promotes adipocyte differentiation in mesenchymal progenitor cells, ROB-C26. Histochem Cell Biol 138(6):833–845. https://doi.org/10.1007/s00418-012-1007-3
Article
CAS
PubMed
Google Scholar
He Q, Huang HY, Zhang YY, Li X, Qian SW, Tang QQ (2012) TAZ is downregulated by dexamethasone during the differentiation of 3T3-L1 preadipocytes. Biochem Biophys Res Commun 419(3):573–577. https://doi.org/10.1016/j.bbrc.2012.02.074
Article
CAS
PubMed
Google Scholar
Wang GJ, Cui Q, Balian G (2000) The nicolas andry award. The pathogenesis and prevention of steroid-induced osteonecrosis. Clin Orthop Relat Res 370:295–310
Article
Google Scholar
Mikami Y, Lee M, Irie S, Honda MJ (2011) Dexamethasone modulates osteogenesis and adipogenesis with regulation of osterix expression in rat calvaria-derived cells. J Cell Physiol 226(3):739–748. https://doi.org/10.1002/jcp.22392
Article
CAS
PubMed
Google Scholar
Hara ES, Ono M, Pham HT, Sonoyama W, Kubota S, Takigawa M, Matsumoto T, Young MF, Olsen BR, Kuboki T (2015) Fluocinolone acetonide is a potent synergistic factor of TGF-beta3-associated chondrogenesis of bone marrow-derived mesenchymal stem cells for articular surface regeneration. J Bone Miner Res 30(9):1585–1596. https://doi.org/10.1002/jbmr.2502
Article
CAS
PubMed
Google Scholar
Zhang YY, Li X, Qian SW, Guo L, Huang HY, He Q, Liu Y, Ma CG, Tang QQ (2012) Down-regulation of type I Runx2 mediated by dexamethasone is required for 3T3-L1 adipogenesis. Mol Endocrinol 26(5):798–808. https://doi.org/10.1210/me.2011-1287
Article
CAS
PubMed
PubMed Central
Google Scholar
Li J, Zhang N, Huang X, Xu J, Fernandes JC, Dai K, Zhang X (2013) Dexamethasone shifts bone marrow stromal cells from osteoblasts to adipocytes by C/EBPalpha promoter methylation. Cell Death Disease 4:e832. https://doi.org/10.1038/cddis.2013.348
Article
CAS
PubMed
PubMed Central
Google Scholar
Correa D, Somoza RA, Lin P, Greenberg S, Rom E, Duesler L, Welter JF, Yayon A, Caplan AI (2015) Sequential exposure to fibroblast growth factors (FGF) 2, 9 and 18 enhances hMSC chondrogenic differentiation. Osteoarthr Res Soc 23(3):443–453. https://doi.org/10.1016/j.joca.2014.11.013
Article
CAS
Google Scholar
Le Blanc S, Simann M, Jakob F, Schutze N, Schilling T (2015) Fibroblast growth factors 1 and 2 inhibit adipogenesis of human bone marrow stromal cells in 3D collagen gels. Exp Cell Res 338(2):136–148. https://doi.org/10.1016/j.yexcr.2015.09.009
Article
CAS
PubMed
Google Scholar
Pizzute T, Li JT, Zhang Y, Davis ME, Pei M (2016) Fibroblast growth factor ligand dependent proliferation and chondrogenic differentiation of synovium-derived stem cells and concomitant adaptation of wnt/mitogen-activated protein kinase signals. Tissue Eng Pt A 22(15–16):1036–1046
Article
CAS
Google Scholar
Solchaga LA, Penick K, Goldberg VM, Caplan AI, Welter JF (2010) Fibroblast growth factor-2 enhances proliferation and delays loss of chondrogenic potential in human adult bone-marrow-derived mesenchymal stem cells. Tissue Eng Part A 16(3):1009–1019
Article
PubMed
Google Scholar
Kim JH, Lee MC, Seong SC, Park KH, Lee S (2011) Enhanced Proliferation and chondrogenic differentiation of human synovium-derived stem cells expanded with basic fibroblast growth factor. Tissue Eng Part A 17(7–8):991–1002
Article
CAS
PubMed
Google Scholar
Solchaga LA, Penick K, Porter JD, Goldberg VM, Caplan AI, Welter JF (2005) FGF-2 enhances the mitotic and chondrogenic potentials of human adult bone marrow-derived mesenchymal stem cells. J Cell Physiol 203(2):398–409
Article
CAS
PubMed
Google Scholar
Buckley CT, Kelly DJ (2012) Expansion in the presence of FGF-2 enhances the functional development of cartilaginous tissues engineered using infrapatellar fat pad derived MSCs. J Mech Behav Biomed 11:102–111
Article
CAS
Google Scholar
Cheng T, Yang C, Weber N, Kim HT, Kuo AC (2012) Fibroblast growth factor 2 enhances the kinetics of mesenchymal stem cell chondrogenesis. Biochem Biophys Res Commun 426(4):544–550
Article
CAS
PubMed
Google Scholar
Bianchessi M, Chen Y, Durgam S, Pondenis H, Stewart M (2016) Effect of fibroblast growth factor 2 on equine synovial fluid chondroprogenitor expansion and chondrogenesis. Stem Cells Int 2016:9364974. https://doi.org/10.1155/2016/9364974
Article
CAS
PubMed
Google Scholar
Coipeau P, Rosset P, Langonne A, Gaillard J, Delorme B, Rico A, Domenech J, Charbord P, Sensebe L (2009) Impaired differentiation potential of human trabecular bone mesenchymal stromal cells from elderly patients. Cytotherapy 11(5):584–594
Article
CAS
PubMed
Google Scholar
Weiss S, Hennig T, Bock R, Steck E, Richter W (2010) Impact of growth factors and PTHrP on early and late chondrogenic differentiation of human mesenchymal stem cells. J Cell Physiol 223(1):84–93. https://doi.org/10.1002/jcp.22013
CAS
Article
PubMed
Google Scholar
Hildner F, Peterbauer A, Wolbank S, Nurnberger S, Marlovits S, Redl H, van Griensven M, Gabriel C (2010) FGF-2 abolishes the chondrogenic effect of combined BMP-6 and TGF-beta in human adipose derived stem cells. J Biomed Mater Res, Part A 94(3):978–987. https://doi.org/10.1002/jbm.a.32761
CAS
Article
Google Scholar
Bosetti M, Boccafoschi F, Leigheb M, Bianchi AE, Cannas M (2012) Chondrogenic induction of human mesenchymal stem cells using combined growth factors for cartilage tissue engineering. J Tissue Eng Regen Med 6(3):205–213. https://doi.org/10.1002/term.416
Article
CAS
PubMed
Google Scholar
Hutley L, Shurety W, Newell F, McGeary R, Pelton N, Grant J, Herington A, Cameron D, Whitehead J, Prins J (2004) Fibroblast growth factor 1: a key regulator of human adipogenesis. Diabetes 53(12):3097–3106
Article
CAS
PubMed
Google Scholar
Neubauer M, Fischbach C, Bauer-Kreisel P, Lieb E, Hacker M, Tessmar J, Schulz MB, Goepferich A, Blunk T (2004) Basic fibroblast growth factor enhances PPARgamma ligand-induced adipogenesis of mesenchymal stem cells. FEBS Lett 577(1–2):277–283. https://doi.org/10.1016/j.febslet.2004.10.020
Article
CAS
PubMed
Google Scholar
Inoue S, Hori Y, Hirano Y, Inamoto T, Tabata Y (2005) Effect of culture substrate and fibroblast growth factor addition on the proliferation and differentiation of human adipo-stromal cells. J Biomater Sci Polym Ed 16(1):57–77
Article
CAS
PubMed
Google Scholar
Kakudo N, Shimotsuma A, Kusumoto K (2007) Fibroblast growth factor-2 stimulates adipogenic differentiation of human adipose-derived stem cells. Biochem Biophys Res Commun 359(2):239–244. https://doi.org/10.1016/j.bbrc.2007.05.070
Article
CAS
PubMed
Google Scholar
Prusty D, Park BH, Davis KE, Farmer SR (2002) Activation of MEK/ERK signaling promotes adipogenesis by enhancing peroxisome proliferator-activated receptor gamma (PPARgamma) and C/EBPalpha gene expression during the differentiation of 3T3-L1 preadipocytes. J Biol Chem 277(48):46226–46232. https://doi.org/10.1074/jbc.M207776200
Article
CAS
PubMed
Google Scholar
Kalomoiris S, Cicchetto AC, Lakatos K, Nolta JA, Fierro FA (2016) Fibroblast growth factor 2 regulates high mobility group A2 expression in human bone marrow-derived mesenchymal stem cells. J Cell Biochem 117(9):2128–2137. https://doi.org/10.1002/jcb.25519
Article
CAS
PubMed
PubMed Central
Google Scholar
Luo X, Hutley LJ, Webster JA, Kim YH, Liu DF, Newell FS, Widberg CH, Bachmann A, Turner N, Schmitz-Peiffer C, Prins JB, Yang GS, Whitehead JP (2012) Identification of BMP and activin membrane-bound inhibitor (BAMBI) as a potent negative regulator of adipogenesis and modulator of autocrine/paracrine adipogenic factors. Diabetes 61(1):124–136. https://doi.org/10.2337/db11-0998
Article
CAS
PubMed
Google Scholar
Ullrich A, Schlessinger J (1990) Signal transduction by receptors with tyrosine kinase activity. Cell 61(2):203–212
Article
CAS
PubMed
Google Scholar
Frisch J, Venkatesan JK, Rey-Rico A, Schmitt G, Madry H, Cucchiarini M (2014) Influence of insulin-like growth factor I overexpression via recombinant adeno-associated vector gene transfer upon the biological activities and differentiation potential of human bone marrow-derived mesenchymal stem cells. Stem Cell Res Ther 5(4):103. https://doi.org/10.1186/scrt491
Article
PubMed
PubMed Central
Google Scholar
Frisch J, Rey-Rico A, Venkatesan JK, Schmitt G, Madry H, Cucchiarini M (2015) Chondrogenic differentiation processes in human bone marrow aspirates upon rAAV-mediated gene transfer and overexpression of the insulin-like growth factor I. Tissue Eng Part A 21(17–18):2460–2471. https://doi.org/10.1089/ten.TEA.2014.0679
Article
CAS
PubMed
PubMed Central
Google Scholar
Giorgetti S, Ballotti R, Kowalski-Chauvel A, Tartare S, Van Obberghen E (1993) The insulin and insulin-like growth factor-I receptor substrate IRS-1 associates with and activates phosphatidylinositol 3-kinase in vitro. J Biol Chem 268(10):7358–7364
CAS
PubMed
Google Scholar
Phornphutkul C, Wu KY, Yang X, Chen Q, Gruppuso PA (2004) Insulin-like growth factor-I signaling is modified during chondrocyte differentiation. J Endocrinol 183(3):477–486. https://doi.org/10.1677/joe.1.05873
Article
CAS
PubMed
Google Scholar
Starkman BG, Cravero JD, Delcarlo M, Loeser RF (2005) IGF-I stimulation of proteoglycan synthesis by chondrocytes requires activation of the PI 3-kinase pathway but not ERK MAPK. Biochem J 389(Pt 3):723–729. https://doi.org/10.1042/BJ20041636
Article
CAS
PubMed
PubMed Central
Google Scholar
Boney CM, Smith RM, Gruppuso PA (1998) Modulation of insulin-like growth factor I mitogenic signaling in 3T3-L1 preadipocyte differentiation. Endocrinology 139(4):1638–1644. https://doi.org/10.1210/endo.139.4.5920
Article
CAS
PubMed
Google Scholar
Boney CM, Gruppuso PA, Faris RA, Frackelton AR Jr (2000) The critical role of Shc in insulin-like growth factor-I-mediated mitogenesis and differentiation in 3T3-L1 preadipocytes. Mol Endocrinol 14(6):805–813. https://doi.org/10.1210/mend.14.6.0487
Article
CAS
PubMed
Google Scholar
Oh CD, Chun JS (2003) Signaling mechanisms leading to the regulation of differentiation and apoptosis of articular chondrocytes by insulin-like growth factor-1. J Biol Chem 278(38):36563–36571. https://doi.org/10.1074/jbc.M304857200
Article
CAS
PubMed
Google Scholar
McMahon LA, Prendergast PJ, Campbell VA (2008) A comparison of the involvement of p38, ERK1/2 and PI3K in growth factor-induced chondrogenic differentiation of mesenchymal stem cells. Biochem Biophys Res Commun 368(4):990–995. https://doi.org/10.1016/j.bbrc.2008.01.160
Article
CAS
PubMed
Google Scholar
Zhang L, Grennan-Jones F, Draman MS, Lane C, Morris D, Dayan CM, Tee AR, Ludgate M (2014) Possible targets for nonimmunosuppressive therapy of Graves’ orbitopathy. J Clin Endocrinol Metab 99(7):E1183–E1190. https://doi.org/10.1210/jc.2013-4182
Article
CAS
PubMed
Google Scholar
Miki H, Yamauchi T, Suzuki R, Komeda K, Tsuchida A, Kubota N, Terauchi Y, Kamon J, Kaburagi Y, Matsui J, Akanuma Y, Nagai R, Kimura S, Tobe K, Kadowaki T (2001) Essential role of insulin receptor substrate 1 (IRS-1) and IRS-2 in adipocyte differentiation. Mol Cell Biol 21(7):2521–2532. https://doi.org/10.1128/MCB.21.7.2521-2532.2001
Article
CAS
PubMed
PubMed Central
Google Scholar
Viti F, Landini M, Mezzelani A, Petecchia L, Milanesi L, Scaglione S (2016) Osteogenic differentiation of MSC through calcium signaling activation: transcriptomics and functional analysis. PLoS One 11(2):e0148173. https://doi.org/10.1371/journal.pone.0148173
Article
CAS
PubMed
PubMed Central
Google Scholar
Kawano S, Shoji S, Ichinose S, Yamagata K, Tagami M, Hiraoka M (2002) Characterization of Ca(2 +) signaling pathways in human mesenchymal stem cells. Cell Calcium 32(4):165–174
Article
CAS
PubMed
Google Scholar
Dry H, Jorgenson K, Ando W, Hart DA, Frank CB, Sen A (2013) Effect of calcium on the proliferation kinetics of synovium-derived mesenchymal stromal cells. Cytotherapy 15(7):805–819. https://doi.org/10.1016/j.jcyt.2013.01.011
Article
CAS
PubMed
Google Scholar
Mellor LF, Mohiti-Asli M, Williams J, Kannan A, Dent MR, Guilak F, Loboa EG (2015) Extracellular calcium modulates chondrogenic and osteogenic differentiation of human adipose-derived stem cells: a novel approach for osteochondral tissue engineering using a single stem cell source. Tissue Eng Part A 21(17–18):2323–2333. https://doi.org/10.1089/ten.TEA.2014.0572
Article
CAS
PubMed
PubMed Central
Google Scholar
Parate D, Franco-Obregon A, Frohlich J, Beyer C, Abbas AA, Kamarul T, Hui JHP, Yang Z (2017) Enhancement of mesenchymal stem cell chondrogenesis with short-term low intensity pulsed electromagnetic fields. Sci Rep 7(1):9421. https://doi.org/10.1038/s41598-017-09892-w
Article
CAS
PubMed
PubMed Central
Google Scholar
Steward AJ, Kelly DJ, Wagner DR (2014) The role of calcium signalling in the chondrogenic response of mesenchymal stem cells to hydrostatic pressure. Eur Cells Mater 28:358–371
Article
CAS
Google Scholar
Kwon HJ, Lee GS, Chun H (2016) Electrical stimulation drives chondrogenesis of mesenchymal stem cells in the absence of exogenous growth factors. Sci Rep 6:39302. https://doi.org/10.1038/srep39302
Article
CAS
PubMed
PubMed Central
Google Scholar
Holzer P (2011) Transient receptor potential (TRP) channels as drug targets for diseases of the digestive system. Pharmacol Ther 131(1):142–170. https://doi.org/10.1016/j.pharmthera.2011.03.006
Article
CAS
PubMed
PubMed Central
Google Scholar
Pall ML (2013) Electromagnetic fields act via activation of voltage-gated calcium channels to produce beneficial or adverse effects. J Cell Mol Med 17(8):958–965. https://doi.org/10.1111/jcmm.12088
Article
CAS
PubMed
PubMed Central
Google Scholar
Shi H, Halvorsen YD, Ellis PN, Wilkison WO, Zemel MB (2000) Role of intracellular calcium in human adipocyte differentiation. Physiol Genom 3(2):75–82. https://doi.org/10.1152/physiolgenomics.2000.3.2.75
Article
CAS
Google Scholar
Jensen B, Farach-Carson MC, Kenaley E, Akanbi KA (2004) High extracellular calcium attenuates adipogenesis in 3T3-L1 preadipocytes. Exp Cell Res 301(2):280–292. https://doi.org/10.1016/j.yexcr.2004.08.030
Article
CAS
PubMed
Google Scholar
Hashimoto R, Katoh Y, Miyamoto Y, Itoh S, Daida H, Nakazato Y, Okada T (2015) Increased extracellular and intracellular Ca(2)(+) lead to adipocyte accumulation in bone marrow stromal cells by different mechanisms. Biochem Biophys Res Commun 457(4):647–652. https://doi.org/10.1016/j.bbrc.2015.01.042
Article
CAS
PubMed
Google Scholar
Hashimoto R, Katoh Y, Nakamura K, Itoh S, Iesaki T, Daida H, Nakazato Y, Okada T (2012) Enhanced accumulation of adipocytes in bone marrow stromal cells in the presence of increased extracellular and intracellular [Ca(2)(+)]. Biochem Biophys Res Commun 423(4):672–678. https://doi.org/10.1016/j.bbrc.2012.06.010
Article
CAS
PubMed
Google Scholar
Hashimoto R, Katoh Y, Miyamoto Y, Nakamura K, Itoh S, Daida H, Nakazato Y, Okada T (2017) High extracellular Ca(2 +) enhances the adipocyte accumulation of bone marrow stromal cells through a decrease in cAMP. Cell Calcium 67:74–80. https://doi.org/10.1016/j.ceca.2017.08.006
Article
CAS
PubMed
Google Scholar
Zhang F, Ye J, Meng Y, Ai W, Su H, Zheng J, Liu F, Zhu X, Wang L, Gao P, Shu G, Jiang Q, Wang S (2018) Calcium supplementation enhanced adipogenesis and improved glucose homeostasis through activation of Camkii and PI3K/Akt signaling pathway in porcine bone marrow mesenchymal stem cells (pBMSCs) and mice fed high fat diet (HFD). Cellular Physiol Biochem 51(1):154–172. https://doi.org/10.1159/000495171
Article
CAS
Google Scholar
Bae YK, Kwon JH, Kim M, Kim GH, Choi SJ, Oh W, Yang YS, Jin HJ, Jeon HB (2018) Intracellular Calcium determines the adipogenic differentiation potential of human umbilical cord blood-derived mesenchymal stem cells via the Wnt5a/beta-Catenin signaling pathway. Stem Cells Int 2018:6545071. https://doi.org/10.1155/2018/6545071
Article
PubMed
PubMed Central
Google Scholar
Gao L, McBeath R, Chen CS (2010) Stem cell shape regulates a chondrogenic versus myogenic fate through Rac1 and N-cadherin. Stem Cells 28(3):564–572. https://doi.org/10.1002/stem.308
CAS
Article
PubMed
PubMed Central
Google Scholar
Shao HJ, Ho CC, Lee YT, Chen CS, Wang JH, Young TH (2012) Chondrogenesis of human bone marrow mesenchymal cells by transforming growth factors beta1 through cell shape changes on controlled biomaterials. J Biomed Mater Res, Part A 100(12):3344–3352. https://doi.org/10.1002/jbm.a.34291
Article
CAS
Google Scholar
Chang KH, Liao HT, Chen JP (2013) Preparation and characterization of gelatin/hyaluronic acid cryogels for adipose tissue engineering: in vitro and in vivo studies. Acta Biomater 9(11):9012–9026. https://doi.org/10.1016/j.actbio.2013.06.046
Article
CAS
PubMed
Google Scholar
Mathieu PS, Loboa EG (2012) Cytoskeletal and focal adhesion influences on mesenchymal stem cell shape, mechanical properties, and differentiation down osteogenic, adipogenic, and chondrogenic pathways. Tissue Eng Part B Rev 18(6):436–444. https://doi.org/10.1089/ten.TEB.2012.0014
Article
CAS
PubMed
PubMed Central
Google Scholar
McBeath R, Pirone DM, Nelson CM, Bhadriraju K, Chen CS (2004) Cell shape, cytoskeletal tension, and RhoA regulate stem cell lineage commitment. Dev Cell 6(4):483–495
Article
CAS
PubMed
Google Scholar
Zhang Y, Chen S, Pei M (2016) Biomechanical signals guiding stem cell cartilage engineering: from molecular adaption to tissue functionality. Eur Cells Mater 31:59–78
Article
CAS
Google Scholar
Engler AJ, Sen S, Sweeney HL, Discher DE (2006) Matrix elasticity directs stem cell lineage specification. Cell 126(4):677–689. https://doi.org/10.1016/j.cell.2006.06.044
Article
CAS
PubMed
Google Scholar
Schwarz S, Elsaesser AF, Koerber L, Goldberg-Bockhorn E, Seitz AM, Bermueller C, Durselen L, Ignatius A, Breiter R, Rotter N (2015) Processed xenogenic cartilage as innovative biomatrix for cartilage tissue engineering: effects on chondrocyte differentiation and function. J Tissue Eng Regen Med 9(12):E239–E251. https://doi.org/10.1002/term.1650
Article
CAS
PubMed
Google Scholar
Garrigues NW, Little D, Sanchez-Adams J, Ruch DS, Guilak F (2014) Electrospun cartilage-derived matrix scaffolds for cartilage tissue engineering. J Biomed Mater Res, Part A 102(11):3998–4008. https://doi.org/10.1002/jbm.a.35068
Article
CAS
Google Scholar
Park JS, Chu JS, Tsou AD, Diop R, Tang Z, Wang A, Li S (2011) The effect of matrix stiffness on the differentiation of mesenchymal stem cells in response to TGF-beta. Biomaterials 32(16):3921–3930. https://doi.org/10.1016/j.biomaterials.2011.02.019
Article
CAS
PubMed
PubMed Central
Google Scholar
Young DA, Choi YS, Engler AJ, Christman KL (2013) Stimulation of adipogenesis of adult adipose-derived stem cells using substrates that mimic the stiffness of adipose tissue. Biomaterials 34(34):8581–8588. https://doi.org/10.1016/j.biomaterials.2013.07.103
Article
CAS
PubMed
PubMed Central
Google Scholar
Hwang JH, Byun MR, Kim AR, Kim KM, Cho HJ, Lee YH, Kim J, Jeong MG, Hwang ES, Hong JH (2015) Extracellular matrix stiffness regulates osteogenic differentiation through MAPK activation. PLoS One 10(8):e0135519. https://doi.org/10.1371/journal.pone.0135519
Article
CAS
PubMed
PubMed Central
Google Scholar
Ye K, Cao L, Li S, Yu L, Ding J (2016) Interplay of matrix stiffness and cell-cell contact in regulating differentiation of stem cells. ACS Appl Mater Interfaces 8(34):21903–21913. https://doi.org/10.1021/acsami.5b09746
Article
CAS
PubMed
Google Scholar
Hendriks JA, Moroni L, Riesle J, de Wijn JR, van Blitterswijk CA (2013) The effect of scaffold-cell entrapment capacity and physico-chemical properties on cartilage regeneration. Biomaterials 34(17):4259–4265. https://doi.org/10.1016/j.biomaterials.2013.02.060
Article
CAS
PubMed
Google Scholar
Younesi M, Goldberg VM, Akkus O (2016) A micro-architecturally biomimetic collagen template for mesenchymal condensation based cartilage regeneration. Acta Biomater 30:212–221. https://doi.org/10.1016/j.actbio.2015.11.024
Article
CAS
PubMed
Google Scholar
Muller WE, Neufurth M, Wang S, Tolba E, Schroder HC, Wang X (2016) Morphogenetically active scaffold for osteochondral repair (polyphosphate/alginate/N, O-carboxymethyl chitosan). Eur Cells Mater 31:174–190
Article
CAS
Google Scholar
Kim JS, Choi JS, Cho YW (2017) Cell-free hydrogel system based on a tissue-specific extracellular matrix for in situ adipose tissue regeneration. ACS Appl Mater Interfaces 9(10):8581–8588. https://doi.org/10.1021/acsami.6b16783
Article
CAS
PubMed
Google Scholar
Zhao W, Li X, Liu X, Zhang N, Wen X (2014) Effects of substrate stiffness on adipogenic and osteogenic differentiation of human mesenchymal stem cells. Mater Sci Eng C 40:316–323. https://doi.org/10.1016/j.msec.2014.03.048
Article
CAS
Google Scholar
Shoham N, Girshovitz P, Katzengold R, Shaked NT, Benayahu D, Gefen A (2014) Adipocyte stiffness increases with accumulation of lipid droplets. Biophys J 106(6):1421–1431. https://doi.org/10.1016/j.bpj.2014.01.045
Article
CAS
PubMed
PubMed Central
Google Scholar
Lim YB, Kang SS, Park TK, Lee YS, Chun JS, Sonn JK (2000) Disruption of actin cytoskeleton induces chondrogenesis of mesenchymal cells by activating protein kinase C-alpha signaling. Biochem Biophys Res Commun 273(2):609–613. https://doi.org/10.1006/bbrc.2000.2987
Article
CAS
PubMed
Google Scholar
Woods A, Beier F (2006) RhoA/ROCK signaling regulates chondrogenesis in a context-dependent manner. J Biol Chem 281(19):13134–13140. https://doi.org/10.1074/jbc.M509433200
Article
CAS
PubMed
Google Scholar
Campbell JJ, Lee DA, Bader DL (2006) Dynamic compressive strain influences chondrogenic gene expression in human mesenchymal stem cells. Biorheology 43(4):455–470
PubMed
Google Scholar
Kupcsik L, Stoddart MJ, Li Z, Benneker LM, Alini M (2010) Improving chondrogenesis: potential and limitations of SOX9 gene transfer and mechanical stimulation for cartilage tissue engineering. Tissue Eng Part A 16(6):1845–1855. https://doi.org/10.1089/ten.TEA.2009.0531
Article
CAS
PubMed
Google Scholar
Li Z, Kupcsik L, Yao SJ, Alini M, Stoddart MJ (2010) Mechanical load modulates chondrogenesis of human mesenchymal stem cells through the TGF-beta pathway. J Cell Mol Med 14(6A):1338–1346. https://doi.org/10.1111/j.1582-4934.2009.00780.x
Article
CAS
PubMed
Google Scholar
Zhang T, Wen F, Wu Y, Goh GS, Ge Z, Tan LP, Hui JH, Yang Z (2015) Cross-talk between TGF-beta/SMAD and integrin signaling pathways in regulating hypertrophy of mesenchymal stem cell chondrogenesis under deferral dynamic compression. Biomaterials 38:72–85. https://doi.org/10.1016/j.biomaterials.2014.10.010
Article
CAS
PubMed
Google Scholar
Bian L, Zhai DY, Zhang EC, Mauck RL, Burdick JA (2012) Dynamic compressive loading enhances cartilage matrix synthesis and distribution and suppresses hypertrophy in hMSC-laden hyaluronic acid hydrogels. Tissue Eng Part A 18(7–8):715–724. https://doi.org/10.1089/ten.TEA.2011.0455
Article
CAS
PubMed
Google Scholar
Hossain MG, Iwata T, Mizusawa N, Shima SW, Okutsu T, Ishimoto K, Yoshimoto K (2010) Compressive force inhibits adipogenesis through COX-2-mediated down-regulation of PPARgamma2 and C/EBPalpha. J Biosci Bioeng 109(3):297–303. https://doi.org/10.1016/j.jbiosc.2009.09.003
Article
CAS
PubMed
Google Scholar
Arnsdorf EJ, Tummala P, Kwon RY, Jacobs CR (2009) Mechanically induced osteogenic differentiation–the role of RhoA, ROCKII and cytoskeletal dynamics. J Cell Sci 122(Pt 4):546–553. https://doi.org/10.1242/jcs.036293
Article
CAS
PubMed
PubMed Central
Google Scholar
Zhong W, Tian K, Zheng X, Li L, Zhang W, Wang S, Qin J (2013) Mesenchymal stem cell and chondrocyte fates in a multishear microdevice are regulated by yes-associated protein. Stem Cells Dev 22(14):2083–2093. https://doi.org/10.1089/scd.2012.0685
Article
CAS
PubMed
Google Scholar
Khan WS, Adesida AB, Hardingham TE (2007) Hypoxic conditions increase hypoxia-inducible transcription factor 2alpha and enhance chondrogenesis in stem cells from the infrapatellar fat pad of osteoarthritis patients. Arthritis Res Ther 9(3):R55. https://doi.org/10.1186/ar2211
Article
CAS
PubMed
PubMed Central
Google Scholar
Kanichai M, Ferguson D, Prendergast PJ, Campbell VA (2008) Hypoxia promotes chondrogenesis in rat mesenchymal stem cells: a role for AKT and hypoxia-inducible factor (HIF)-1alpha. J Cell Physiol 216(3):708–715. https://doi.org/10.1002/jcp.21446
Article
CAS
PubMed
Google Scholar
Khan WS, Adesida AB, Tew SR, Lowe ET, Hardingham TE (2010) Bone marrow-derived mesenchymal stem cells express the pericyte marker 3G5 in culture and show enhanced chondrogenesis in hypoxic conditions. J Orthop Res 28(6):834–840. https://doi.org/10.1002/jor.21043
CAS
Article
PubMed
Google Scholar
Adesida AB, Mulet-Sierra A, Jomha NM (2012) Hypoxia mediated isolation and expansion enhances the chondrogenic capacity of bone marrow mesenchymal stromal cells. Stem Cell Res Ther 3(2):9. https://doi.org/10.1186/scrt100
Article
CAS
PubMed
PubMed Central
Google Scholar
Merceron C, Vinatier C, Portron S, Masson M, Amiaud J, Guigand L, Cherel Y, Weiss P, Guicheux J (2010) Differential effects of hypoxia on osteochondrogenic potential of human adipose-derived stem cells. Am J Physiol Cell Physiol 298(2):C355–C364. https://doi.org/10.1152/ajpcell.00398.2009
Article
CAS
PubMed
Google Scholar
Cicione C, Muinos-Lopez E, Hermida-Gomez T, Fuentes-Boquete I, Diaz-Prado S, Blanco FJ (2013) Effects of severe hypoxia on bone marrow mesenchymal stem cells differentiation potential. Stem Cells Int 2013:232896. https://doi.org/10.1155/2013/232896
Article
CAS
PubMed
PubMed Central
Google Scholar
Yun Z, Maecker HL, Johnson RS, Giaccia AJ (2002) Inhibition of PPAR gamma 2 gene expression by the HIF-1-regulated gene DEC1/Stra13: a mechanism for regulation of adipogenesis by hypoxia. Dev Cell 2(3):331–341
Article
CAS
PubMed
Google Scholar
Kim KH, Song MJ, Chung J, Park H, Kim JB (2005) Hypoxia inhibits adipocyte differentiation in a HDAC-independent manner. Biochem Biophys Res Commun 333(4):1178–1184. https://doi.org/10.1016/j.bbrc.2005.06.023
Article
CAS
PubMed
Google Scholar
Gentil C, Le Jan S, Philippe J, Leibowitch J, Sonigo P, Germain S, Pietri-Rouxel F (2006) Is oxygen a key factor in the lipodystrophy phenotype? Lipids Health Disease 5:27. https://doi.org/10.1186/1476-511X-5-27
Article
CAS
Google Scholar
Itoigawa Y, Kishimoto KN, Okuno H, Sano H, Kaneko K, Itoi E (2010) Hypoxia induces adipogenic differentitation of myoblastic cell lines. Biochem Biophys Res Commun 399(4):721–726. https://doi.org/10.1016/j.bbrc.2010.08.007
Article
CAS
PubMed
Google Scholar
Weiszenstein M, Musutova M, Plihalova A, Westlake K, Elkalaf M, Koc M, Prochazka A, Pala J, Gulati S, Trnka J, Polak J (2016) Adipogenesis, lipogenesis and lipolysis is stimulated by mild but not severe hypoxia in 3T3-L1 cells. Biochem Biophys Res Commun 478(2):727–732. https://doi.org/10.1016/j.bbrc.2016.08.015
Article
CAS
PubMed
Google Scholar
Jiang C, Sun J, Dai Y, Cao P, Zhang L, Peng S, Zhou Y, Li G, Tang J, Xiang J (2015) HIF-1A and C/EBPs transcriptionally regulate adipogenic differentiation of bone marrow-derived MSCs in hypoxia. Stem Cell Res Ther 6:21. https://doi.org/10.1186/s13287-015-0014-4
Article
CAS
PubMed
PubMed Central
Google Scholar
Fehrer C, Brunauer R, Laschober G, Unterluggauer H, Reitinger S, Kloss F, Gully C, Gassner R, Lepperdinger G (2007) Reduced oxygen tension attenuates differentiation capacity of human mesenchymal stem cells and prolongs their lifespan. Aging Cell 6(6):745–757. https://doi.org/10.1111/j.1474-9726.2007.00336.x
Article
CAS
PubMed
Google Scholar
Valorani MG, Germani A, Otto WR, Harper L, Biddle A, Khoo CP, Lin WR, Hawa MI, Tropel P, Patrizi MP, Pozzilli P, Alison MR (2010) Hypoxia increases Sca-1/CD44 co-expression in murine mesenchymal stem cells and enhances their adipogenic differentiation potential. Cell Tissue Res 341(1):111–120. https://doi.org/10.1007/s00441-010-0982-8
Article
CAS
PubMed
Google Scholar
Valorani MG, Montelatici E, Germani A, Biddle A, D’Alessandro D, Strollo R, Patrizi MP, Lazzari L, Nye E, Otto WR, Pozzilli P, Alison MR (2012) Pre-culturing human adipose tissue mesenchymal stem cells under hypoxia increases their adipogenic and osteogenic differentiation potentials. Cell Prolif 45(3):225–238. https://doi.org/10.1111/j.1365-2184.2012.00817.x
Article
CAS
PubMed
PubMed Central
Google Scholar
Ranera B, Remacha AR, Alvarez-Arguedas S, Castiella T, Vazquez FJ, Romero A, Zaragoza P, Martin-Burriel I, Rodellar C (2013) Expansion under hypoxic conditions enhances the chondrogenic potential of equine bone marrow-derived mesenchymal stem cells. Vet J 195(2):248–251. https://doi.org/10.1016/j.tvjl.2012.06.008
Article
PubMed
Google Scholar
Duval E, Bauge C, Andriamanalijaona R, Benateau H, Leclercq S, Dutoit S, Poulain L, Galera P, Boumediene K (2012) Molecular mechanism of hypoxia-induced chondrogenesis and its application in in vivo cartilage tissue engineering. Biomaterials 33(26):6042–6051. https://doi.org/10.1016/j.biomaterials.2012.04.061
Article
CAS
PubMed
Google Scholar
Lee HH, Chang CC, Shieh MJ, Wang JP, Chen YT, Young TH, Hung SC (2013) Hypoxia enhances chondrogenesis and prevents terminal differentiation through PI3K/Akt/FoxO dependent anti-apoptotic effect. Sci Rep 3:2683. https://doi.org/10.1038/srep02683
Article
PubMed
PubMed Central
Google Scholar
Lin Q, Gao Z, Alarcon RM, Ye J, Yun Z (2009) A role of miR-27 in the regulation of adipogenesis. The FEBS J 276(8):2348–2358
Article
CAS
PubMed
Google Scholar
Vacanti V, Kong E, Suzuki G, Sato K, Canty JM, Lee T (2005) Phenotypic changes of adult porcine mesenchymal stem cells induced by prolonged passaging in culture. J Cell Physiol 205(2):194–201. https://doi.org/10.1002/jcp.20376
Article
CAS
PubMed
Google Scholar
Erickson IE, van Veen SC, Sengupta S, Kestle SR, Mauck RL (2011) Cartilage matrix formation by bovine mesenchymal stem cells in three-dimensional culture is age-dependent. Clin Orthop Relat Res 469(10):2744–2753. https://doi.org/10.1007/s11999-011-1869-z
Article
PubMed
PubMed Central
Google Scholar
Tan Q, Lui PP, Rui YF (2012) Effect of in vitro passaging on the stem cell-related properties of tendon-derived stem cells-implications in tissue engineering. Stem Cells Dev 21(5):790–800. https://doi.org/10.1089/scd.2011.0160
Article
CAS
PubMed
Google Scholar
Bertolo A, Mehr M, Janner-Jametti T, Graumann U, Aebli N, Baur M, Ferguson SJ, Stoyanov JV (2016) An in vitro expansion score for tissue-engineering applications with human bone marrow-derived mesenchymal stem cells. J Tissue Eng Regen Med 10(2):149–161. https://doi.org/10.1002/term.1734
Article
CAS
PubMed
Google Scholar
Jiang Y, Mishima H, Sakai S, Liu YK, Ohyabu Y, Uemura T (2008) Gene expression analysis of major lineage-defining factors in human bone marrow cells: effect of aging, gender, and age-related disorders. J Orthop Res 26(7):910–917. https://doi.org/10.1002/jor.20623
Article
CAS
PubMed
Google Scholar
Moerman EJ, Teng K, Lipschitz DA, Lecka-Czernik B (2004) Aging activates adipogenic and suppresses osteogenic programs in mesenchymal marrow stroma/stem cells: the role of PPAR-gamma2 transcription factor and TGF-beta/BMP signaling pathways. Aging Cell 3(6):379–389. https://doi.org/10.1111/j.1474-9728.2004.00127.x
Article
CAS
PubMed
Google Scholar
Bonab MM, Alimoghaddam K, Talebian F, Ghaffari SH, Ghavamzadeh A, Nikbin B (2006) Aging of mesenchymal stem cell in vitro. BMC Cell Biol 7:14. https://doi.org/10.1186/1471-2121-7-14
Article
CAS
PubMed
PubMed Central
Google Scholar
Conget PA, Minguell JJ (1999) Phenotypical and functional properties of human bone marrow mesenchymal progenitor cells. J Cell Physiol 181(1):67–73. https://doi.org/10.1002/(SICI)1097-4652(199910)181:1%3c67:AID-JCP7%3e3.0.CO;2-C
Article
CAS
PubMed
Google Scholar
Zhao Y, Waldman SD, Flynn LE (2012) The effect of serial passaging on the proliferation and differentiation of bovine adipose-derived stem cells. Cells, Tissues, Organs 195(5):414–427. https://doi.org/10.1159/000329254
Article
PubMed
Google Scholar
Stenderup K, Justesen J, Clausen C, Kassem M (2003) Aging is associated with decreased maximal life span and accelerated senescence of bone marrow stromal cells. Bone 33(6):919–926
Article
PubMed
Google Scholar
Morse D, Choi AM (2002) Heme oxygenase-1: the “emerging molecule” has arrived. Am J Respir Cell Mol Biol 27(1):8–16. https://doi.org/10.1165/ajrcmb.27.1.4862
Article
CAS
PubMed
Google Scholar
Vanella L, Sodhi K, Kim DH, Puri N, Maheshwari M, Hinds TD, Bellner L, Goldstein D, Peterson SJ, Shapiro JI, Abraham NG (2013) Increased heme-oxygenase 1 expression in mesenchymal stem cell-derived adipocytes decreases differentiation and lipid accumulation via upregulation of the canonical Wnt signaling cascade. Stem Cell Rese Therapy 4(2):28. https://doi.org/10.1186/scrt176
Article
CAS
Google Scholar
Park EJ, Koo OJ, Lee BC (2015) Overexpressed human heme Oxygenase-1 decreases adipogenesis in pigs and porcine adipose-derived stem cells. Biochem Biophys Res Commun 467(4):935–940. https://doi.org/10.1016/j.bbrc.2015.10.040
Article
CAS
PubMed
Google Scholar
Hamedi-Asl P, Halabian R, Bahmani P, Mohammadipour M, Mohammadzadeh M, Roushandeh AM, Jahanian-Najafabadi A, Kuwahara Y, Roudkenar MH (2012) Adenovirus-mediated expression of the HO-1 protein within MSCs decreased cytotoxicity and inhibited apoptosis induced by oxidative stresses. Cell Stress Chaperones 17(2):181–190. https://doi.org/10.1007/s12192-011-0298-y
Article
CAS
PubMed
Google Scholar