Type I collagen deposition via osteoinduction ameliorates YAP/TAZ activity in 3D floating culture clumps of mesenchymal stem cell/extracellular matrix complexes
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Three-dimensional (3D) floating culture clumps of mesenchymal stem cell (MSC)/extracellular matrix (ECM) complexes (C-MSCs) consist of cells and self-produced ECM. Previous studies have demonstrated that C-MSCs can be transplanted into bony lesions without an artificial scaffold to induce bone regeneration. Moreover, osteoinductive medium (OIM)-treated C-MSCs (OIM-C-MSCs) have shown rapid and increased new bone formation in vivo. To apply OIM-C-MSCs for novel bone regenerative cell therapy, their cellular properties at the molecular level must be elucidated. The transcriptional co-activators yes-associated protein/transcriptional co-activator with PDZ-binding motif (YAP/TAZ) have been recognized as key players in the mechanotransduction cascade, controlling cell lineage commitment in MSCs. It is plausible that 3D C-MSCs/OIM-C-MSCs cultured in floating conditions could provide distinct microenvironments compared to conventional 2D culture systems and thereby induce unique mechanotransduction cascades. Therefore, this study investigated the YAP/TAZ activity in 3D-cultured C-MSCs/OIM-C-MSCs in floating conditions.
Human bone marrow-derived MSCs were cultured in growth medium supplemented with ascorbic acid. To obtain C-MSCs, confluent cells that had formed on the cellular sheet were scratched using a micropipette tip and were then torn off. The sheet was rolled to make round clumps of cells. Then, YAP/TAZ activity, filamentous actin (F-actin) integrity, collagen type I (COL1) production, and the differentiation potency in 3D floating culture C-MSCs/OIM-C-MSCs were analyzed.
C-MSCs cultured in floating conditions lost their actin cytoskeleton to downregulate YAP/TAZ activity, which directed cells to undergo adipogenesis/chondrogenesis. OIM treatment induced abundant COL1 deposition, which facilitated Intβ1-dependent actin fiber formation and YAP/TAZ activity to elevate the expression levels of osteogenic master transcriptional factor runt-related transcription factor 2 (RUNX2) mRNA in C-MSCs. Importantly, elevation of YAP/TAZ activity via OIM was associated with COL1 deposition and F-actin integrity, suggesting a positive feedback loop in OIM-C-MSCs.
These findings suggest that OIM-C-MSCs, which form a unique microenvironment that maintains high YAP/TAZ activity, can serve as better candidates for bone regenerative cell therapy than C-MSCs.
KeywordsMechanotransduction 3D culture YAP/TAZ F-actin C-MSCs
Adipogenic induction medium
Activating protein 2
Chondrogenic induction medium
Clumps of mesenchymal stem cells/extracellular matrix proteins
Collagen type I
Connective tissue growth factor
Cysteine-rich angiogenic inducer 61
Dulbecco’s modified Eagle’s medium
Fetal bovine serum
Mesenchymal stem cells
Osteogenic induction medium
Peroxisome proliferator-activated receptor γ
Rho-associated protein kinase
Runt-related transcription factor 2
SRY (sex determining region Y)-box 9
Transcriptional co-activator with PDZ-binding motif
TEA transcriptional factor
Mesenchymal stem cells (MSCs), which possess self-renewing properties, multipotencey, and immunomoduratory potential, are currently the most extensively studied cells for tissue regenerative cell therapy, mainly due to their relative ease of isolation compared to other multipotent cells, such as embryonic stem cells and induced pluripotent stem cells . For the tissue regenerative cell therapy, one of the common approaches is to seed MSCs on scaffold or microcarrier. However, despite recent advances, usage of the artificial scaffolds still harbors several limitations, including biodegradability and host unfavorable inflammatory response . Indeed, our previous study demonstrated that MSC transplantation with osteointegrative biomaterial, β-tricalcium phosphate, induced alveolar bone regeneration in dog class III furcation defect model, though ankylosis, which is an abnormal adhesion of bone and periodontal ligament, was observed . Accordingly, to solve this problem, we recently established clumps of MSC/extracellular matrix (ECM) complexes (C-MSCs), which consist of cells and self-produced ECM [4, 5, 6, 7]. Three-dimensional (3D)-cultured C-MSCs can be grafted into bony lesions without any artificial scaffolds to induce bone regeneration. In addition, osteoinductive medium (OIM)-treated C-MSCs (OIM-C-MSCs) show rapid and increased new bone formation [4, 6]. These previous findings have suggested that OIM-C-MSCs may provide a promising bone regenerative therapy that utilizes cells while avoiding problems associated with the biocompatibility/biodegradability of artificial scaffolds. To develop such a novel cell therapy based on scientific evidence, it is necessary to distinguish the biological capacities of C-MSCs and OIM-C-MSCs at the molecular level.
Compared to traditional cell monolayers cultured on two-dimensional (2D) plastic or glass plates, 3D cultures of C-MSCs could provide markedly different and unique microenvironments for cells. For instance, 2D collagen-coated plastic plates provide a high-stiffness substrate, a continuous layer of ECM, and sufficient space for cells to spread [8, 9]. Conversely, 3D culture systems using various types of gels exhibit decreased stiffness, discrete matrix fibrils, and limited space, restricting cell shapes to a rounded form [8, 9]. Importantly, using mechanotransduction systems, such as those including integrins and cytoskeletal tension, cells can translate physical and mechanical cues into biochemical signals to regulate cell growth and differentiation. Indeed, cell density, cell shape, and matrix elasticity have been shown to direct MSC lineage commitment via cytoskeletal mechanics [10, 11, 12]. Accordingly, it is conceivable that 3D C-MSCs cultured in floating conditions could provide distinct microenvironments compared to conventional 2D culture systems, thereby resulting in the induction of a unique mechanotransduction pathway that regulates cell lineage specification and function.
The transcriptional co-activators yes-associated protein (YAP) and transcriptional co-activator with PDZ-binding motif (TAZ), originally identified as downstream targets of the Hippo signaling pathway [13, 14, 15], have recently been recognized as key factors in the mechanotransduction cascade [16, 17, 18]. Cellular microenvironments that tend to produce high intracellular resistive forces via actin fibers, including an extensive adhesion area, low cell density, stiff ECM, or fluid shear stress, facilitate YAP/TAZ localization to the nucleus to activate their transcriptional activities. In contrast, a narrow adhesion area, high cell density, soft ECM, and disturbed fluid flow produce a low cytoskeletal contractile force by disrupting the integrity of actin fibers, which causes YAP/TAZ cytoplasmic retention and proteasomal degradation [15, 19, 20]. Intriguingly, DuPont et al. reported that MSCs, by sensing the mechanical cues that facilitate the integrity of actin (e.g., stiff ECM), were induced to form osteoblasts via high YAP/TAZ activity, whereas cells cultured on soft ECM or treated with an acto-myosin inhibitor showed low YAP/TAZ activity, consistent with adipogenesis .
Based on these accumulating lines of evidence, we hypothesized that the microenvironment surrounding 3D floating cultured C-MSCs, which should be different from traditional 2D culture, may cause unique mechanotransduction through cytoskeletal mechanics and YAP/TAZ activity, which, in turn, affects the direction of cells’ lineage commitment. Accordingly, the present study investigated (1) filamentous actin (F-actin) fiber integrity and YAP/TAZ activity in 3D floating culture C-MSCs and (2) the effects of OIM on the mechanotransduction cascade that underlies the molecular mechanism of osteogenic induction in C-MSCs.
Materials and methods
C-MSC preparation and culture
siRNAs targeting YAP, TAZ, or negative control siRNA  were chemically synthesized and provided by FASMAC (FASMAC, Kanagawa, Japan). The sequences of these siRNAs are listed in Additional file 1: Table S1. Validated integrin β1 (Intβ1) siRNA was obtained from Invitrogen (#HSS105561; Invitrogen, Carlsbad, CA). Two days before the production of C-MSCs (before scratching), siRNAs were transfected into cells using Lipofectamine RNAi-MAX (Invitrogen) according to the manufacturer’s instructions. Then, the cell sheets were detached and transferred to a 24-well ultra-low-binding plate to generate C-MSCs as described above. The knockdown effects of each siRNA were assessed (Additional file 2: Figure S1A-S1C). All experiments were repeated at least three times independently.
The expression plasmid for HA-TAZS89A was obtained from Addgene (Addgene plasmid 32840; Addgene, Cambridge, MA). An HA expression plasmid was employed as a control (#635688; Clontech, Palo Alto, CA). DNA transfections were performed with ECM 830 (BTX, Holliston, MA). Briefly, after detaching the MSC/ECM complexes from the culture plate, the cell sheet was suspended in 100 μL of Opti-MEM (Invitrogen) with 4 μg of each DNA plasmid and placed into 4-mm-gap cuvettes. Transfections were conducted at 300 V with a 1 ms pulse length and 10 pulses over 5 s. After the pulses, the cell sheets were transferred to a 24-well ultra-low-binding plate to generate C-MSCs, as described above. The effects of each plasmid transfection were assessed (Additional file 2: Figure S1D and S1E). All experiments were repeated at least three times independently.
Induction of C-MSCs
For osteogenic, adipogenic, or chondrogenic induction, the cell sheets were detached from the culture plates and maintained in OIM, adipogenic induction medium (AIM; high-glucose DMEM supplemented with 10% FBS, 0.5 mM isobutylmethylxanthine (Nacalai Tesque, Kyoto, Japan), 0.1 mM indomethacin (Sigma), 1 μM dexamethasone (Sigma), and 10 μg/mL insulin (Sigma)), chondrogenic induction medium (CIM; high-glucose DMEM supplemented with ITS™+ Premix (Corning), 1 mM sodium pyruvate (Sigma), 0.35 mM proline (Sigma), 10 ng/mL transforming growth factor-β3 (Aviscera Bioscience, Santa Clara, CA), 100 nM dexamethasone, and 0.17 mM L-ascorbic acid), or dual induction medium (dual; equal volumes of OIM and AIM)  for 5 days. All experiments were repeated at least three times independently.
C-MSCs were fixed with 4% paraformaldehyde in PBS. The fixed samples were embedded in Tissue-Tek OCT compound (Sakura, Torrance, CA), and 20-μm-thick sections were cut using a cryostat. The sections were washed with PBS and then treated with 5% BSA and 0.1% TWEEN 20 in PBS to block nonspecific staining. These sections were incubated with a rabbit anti-human YAP/TAZ IgG antibody (D24E4; 1:1000; Cell Signaling, Beverly, MA) or rabbit anti-human type I collagen polyclonal IgG (1:200; Novus Biologicals, Littleton, CO) at 4 °C overnight. After being washed 3 times with PBS, samples were incubated for 2 h with an Alexa Fluor 488® goat anti-rabbit IgG antibody (1:100; Invitrogen) and Alexa Fluor 594® phalloidin (1:50; Invitrogen) at room temperature. Then, the nuclei were counterstained with DAPI (5 μg/mL; Invitrogen). After washing the samples with PBS, we detected the fluorescence signals using a Zeiss LSM 5 PASCAL laser scanning confocal microscope (Carl Zeiss Microimaging, Inc., Oberkochen, Germany). To assess YAP/TAZ distribution patterns, we quantified cells in three random fields of view (n = 150~200) as previously described .
The C-MSCs were lysed in buffer containing 25 mM Tris-HCl (pH 7.4), 150 mM NaCl, 5 mM EDTA (pH 8.0), 0.1% SDS, 1% NP-40, 10% glycerol, and 1% (v/v) Triton X-100 . The cell lysates were subjected to ultrasonic treatment for 8 s on ice. Proteins in the lysates were subjected to SDS-PAGE and transferred to a nitrocellulose membrane (Bio-Rad Laboratories, Hercules, CA). The membranes were blocked for 1 h with 5% skim milk and then immunoblotted using rabbit anti-YAP/TAZ IgG (D24E4; 1:1000; Cell Signaling), rabbit anti-YAP IgG (D8H1X; 1:1000; Cell Signaling), rabbit anti-TAZ IgG (V386; 1:1000; Cell Signaling), or mouse anti-β-actin monoclonal antibodies (AC-15; 1:10000; Sigma). The membranes were developed using ECL Plus Western blotting detection reagents (GE Healthcare, Little Chalfont, UK).
For detection of phosphorylated YAP and TAZ, cell lysates were subjected to SDS-PAGE containing a phosphorylation tag (Phos-Tag™, Wako, Osaka, Japan) that specifically traps phosphorylated proteins in the gel. After immunoblotting with anti-YAP or anti-TAZ IgG antibodies, phosphorylated proteins were detected as slower-migrating bands compared to the corresponding unphosphorylated proteins.
Real-time polymerase chain reaction
Total RNA from cultured C-MSCs was extracted using RNA-iso® (Takara, Otsu, Japan) and quantified by spectrometry at 260 and 280 nm. RNA samples (500 ng) were reverse-transcribed into complementary DNA using ReverTra Ace (Toyobo, Osaka, Japan). Then, real-time PCR was performed using a LightCycler and SYBR green (Roche Applied Science, Mannheim, Germany) to determine the relative mRNA expression of collagen type I (COL1), connective tissue growth factor (CTGF), cysteine-rich angiogenic inducer 61 (CYR61), YAP, TAZ, runt-related transcription factor 2 (RUNX2), osteocalcin (OCN), peroxisome proliferator-activated receptor γ (PPARγ), activating protein 2 (AP2), sex determining region Y-box 9 (SOX9), and Aggrecan. The PCR thermal profile consisted of an initial 10 min at 95 °C, followed by 40 cycles of 95 °C for 15 s and 60 °C for 1 min. Fold changes of gene of interest were calculated with ∆∆Ct method using ribosomal protein 18S as reference control. The sequences of the primers used in this study are listed in Additional file 1: Table S2.
Experiments were repeated three or four times, and the results are expressed as the means ± SD. Differences between parameters were tested for statistical significance using unpaired Student’s t tests or ANOVA. Values of p < 0.05 or p < 0.01 were considered significant.
YAP/TAZ activity is downregulated in 3D-cultured C-MSCs
For the generation of 3D-cultured C-MSCs, confluent MSCs treated with ascorbic acid for 4 days were scratched using the tip of a micropipette (Fig. 1a). The MSC/ECM complexes were detached from the culture plate and exhibited a sheet-like morphology (Fig. 1b). After 1 day, this cellular sheet rolled up to form round cell clumps, termed C-MSCs. Immunofluorescence analysis demonstrated that C-MSCs were formed from COL1 produced by the MSCs during the culture period (Fig. 1b). During the C-MSC culture process, F-actin and YAP/TAZ expression patterns were assessed by confocal microscopy. F-actin was thick and abundant at the beginning of C-MSC culture; however, it became thinner and degraded over time, suggesting that F-actin depolymerization occurred in a time-dependent manner (Fig. 1c). In accordance with F-actin depolymerization, YAP/TAZ translocated to the cytoplasm (Fig. 1c, d), and their fluorescence signals were difficult to detect in cultured C-MSCs on day 5 (Fig. 1c). In addition, Western blotting demonstrated that the YAP/TAZ protein levels decreased dramatically on day 1, and this reduction was time-dependent (Fig. 1e). In contrast, their mRNA expression levels were unchanged (Fig. 1f), suggesting that the downregulation of YAP/TAZ in C-MSCs may not be due to transcriptional reduction but instead to proteasomal degradation. It is widely known that phosphorylation of YAP/TAZ leads to their cytoplasmic retention and degradation, which results in the inhibition of YAP/TAZ transcriptional activity. Therefore, next, we measured the phosphorylation levels of YAP/TAZ before their degradation. Notably, YAP/TAZ mobility shifts in a phos-tag gel, suggesting their phosphorylation, were induced in a time-dependent manner after 60 min of detachment (Fig. 1g). Consistent with these findings, the mRNA expression levels of the YAP/TAZ transcriptional target genes CTGF and CYR61 were also markedly decreased on day 1, and the levels remained reduced until the end of the culture period (Fig. 1h). In contrast, MSCs maintained on 2D plastic culture plates kept abundant F-actin fiber structure and demonstrated only slight reductions in YAP/TAZ activity on day 5 (Additional file 2: Figure S2). These findings clearly indicated that YAP/TAZ activity is downregulated in association with actin degradation in 3D floating cultured C-MSCs.
3D-cultured C-MSCs can be directed towards adipogenesis and chondrogenesis, but not osteogenesis, because of reduced YAP/TAZ activity
However, it is possible that our primary MSCs are preferentially directed into adipo-/chondrogenesis instead of osteogenesis. To examine this possibility, we investigated the effects of each induction medium on cells cultured on 2D plastic culture plates at low cell densities were investigated. Consistent with previous studies , subconfluent MSCs on 2D culture plates showed high YAP/TAZ activity (Additional file 2: Figure S3A and S3B). Importantly, 2D-cultured cells demonstrated remarkable increases in osteogenesis but only slight or insufficient adipogenesis and chondrogenesis (Additional file 2: Figure S3C-S3F). In addition, knockdown of YAP/TAZ by siRNA transfection reduced osteogenesis in 2D-cultured MSCs, complementing increases in adipogenesis and chondrogenesis (Additional file 2: Figure S3H-S3J). These findings indicate that our cells possess osteogenic properties in culture conditions with increased YAP/TAZ activity. Therefore, the adipo-/chondrogenic properties of 3D-cultured C-MSCs are due to reduced YAP/TAZ activity.
OIM facilitates F-actin formation and YAP/TAZ activity in C-MSCs
COL1 deposition caused by OIM facilitates a mechanotransduction cascade composed of Intβ1-rho-associated protein kinase (ROCK)-F-actin-YAP/TAZ signaling to induce osteogenesis in C-MSCs
Because ROCK is well established as a downstream target of Intβ1, which facilitates actin polymerization to induce traction force, we next explored the relationship between OIM-induced YAP/TAZ activity and ROCK or the actin cytoskeletal tension using chemical inhibitors. Inhibition of ROCK activity by Y27632 treatment drastically diminished F-actin fibers, consistent with reductions in YAP/TAZ expression levels in OIM-C-MSCs (Fig. 5f). OIM-C-MSCs treated with blebbistatin showed disruption of actin fiber integrity, suggesting a reduction in cytoskeletal tension and degradation of YAP/TAZ (Fig. 5f). YAP/TAZ that had avoided degradation in both Y27632- and blebbistatin-treated groups were mainly localized in the cytoplasm (Fig. 5f, g). Western blotting also showed downregulation of YAP/TAZ expression in OIM-C-MSCs treated with Y27632 and blebbistatin (Fig. 5h). Real-time PCR demonstrated that the YAP/TAZ target genes CTGF and CYR61 were reduced by treatment with these chemical inhibitors as well (Fig. 5i). In addition, RUNX2 mRNA expression levels in OIM-C-MSCs were reduced by ROCK inhibition and F-actin disruption (Fig. 5j). These findings suggested that OIM-induced YAP/TAZ activity was dependent on F-actin fiber integrity regulation by ROCK in 3D-cultured C-MSCs.
YAP/TAZ activity is associated with COL1 synthesis and F-actin formation, generating a positive feedback loop in OIM-C-MSCs
The dominant mechanical cue that occurred during the generation of C-MSCs was the detachment of the cellular sheet from the culture plate. F-actin fibers and YAP/TAZ degradation continued until the end of the C-MSC floating culture period (Fig. 1). In these suspended conditions, it could be challenging to develop sufficient cytoskeletal tension to elevate YAP/TAZ activity in C-MSCs. These findings may suggest that chondrogenic induction of MSCs in vitro preferentially occurs in floating spheroidal culture systems rather than conventional 2D culture on a plastic plate . Because chondrogenesis is abolished by high YAP/TAZ activity , the activity in cells attached to a stiff substrate could be too high to induce successful chondrogenesis.
It has been shown that cell detachment from the culture plate or ECM induced a specific type of apoptosis, termed anoikis. Notably, a recent study demonstrated that the loss of attachment by trypsinization reduced cytoskeletal tension to decrease YAP activity, which resulted in the induction of anoikis . Even though this present study also indicated similar mechanotransduction, few apoptotic cells were observed in floating C-MSCs, as described previously . Because C-MSCs consisted of self-produced ECM that could provide the cells with adhesion conditions, compared with single-cell suspension, YAP/TAZ activity in C-MSCs could be maintained at a slightly higher level to escape anoikis.
OIM, which consists of Dex, AA, and Gly, is a frequently employed culture method for tissue engineering approaches or assessment of the osteogenic differentiation capacity of various cell types . Indeed, OIM has been used to demonstrate the relationship between YAP/TAZ signaling and osteogenesis in vitro [22, 38]. However, few studies documenting the direct effects of OIM on YAP/TAZ activity have been reported. This present study demonstrated that OIM stimulated YAP/TAZ activity to increase RUNX2 mRNA expression in C-MSCs. The key signaling event to induce such YAP/TAZ activity is dependent on an Intβ1-ROCK-F-actin mechanotransduction pathway generated by OIM-induced COL1 deposition. More specifically, we demonstrated that, among the OIM components, the combination of Dex and AA plays a role in COL1 production in association with elevated YAP/TAZ activity in C-MSCs (Fig. 4). Dex upregulates COL1A1 mRNA expression levels in murine and human MSCs [39, 40, 41, 42]. AA increases COL1 mRNA stability  and upregulates secretion of COL1 by inducing proper collagen-triple helix formation . Accordingly, although the precise interaction mechanism of the single elements in OIM is still unclear, Dex and AA may increase COL1 deposition in a coordinated manner to stimulate the YAP/TAZ mechanotransduction pathway in C-MSCs.
The present study revealed that abundant COL1 deposition in OIM-C-MSCs formed a positive feedback loop for YAP/TAZ-regulated mechanotransduction, which was primarily maintained by cytoskeletal tension. In addition, overexpression of TAZS89A also induced a similar feed-forward loop promoting YAP/TAZ activity in C-MSCs. Recently, this type of feed-forward loop of ECM and cytoskeletal tension has been reported in various types of diseases, including cancer , lung fibrosis , liver fibrosis , and pulmonary hypertension [48, 49]. Although aberrant mechanical signaling by YAP/TAZ is associated with the pathogenesis of multiple diseases, YAP/TAZ signaling is also responsible for normal development, organ growth, and tissue regeneration. Therefore, this emerging positive feedback loop of YAP/TAZ may play a role in regulating biological functions in living organisms.
Notably, in contrast to the present study, constitutive active TAZ4SA overexpression in a NIH3T3 mouse fibroblast cell line did not induce ECM deposition or produce a positive feedback loop in other scaffold-free culture systems, i.e., spheroid culture, even though TAZ activity was elevated . The fibroblast spheroids consisted of cells that organize themselves via cell-cell contact. However, no ECM expression was detected in the spheroids by histological analysis. Accordingly, the conflicting findings regarding positive feedback loop formation by transfection of a constitutive active TAZ mutant between C-MSCs and fibroblast spheroids may imply that a certain threshold level of ECM deposition, cytoskeletal tension, and YAP/TAZ activity is essential to generate the feed-forward loop.
Regarding the clinical application of C-MSCs or OIM-C-MSCs for bone regenerative therapy, we reported previously that transplantation of OIM-C-MSCs exerted robust, rapid new bone formation in a bone defect site compared to C-MSCs [4, 6]. This present in vitro study may explain our previous findings. First, C-MSCs, which showed low YAP/TAZ activity, were preferentially induced into adipocytes/chondrocytes but not osteocytes. Second, OIM-C-MSCs showed high YAP/TAZ activity and increased RUNX2 mRNA expression, which are well-known transcription factors for osteogenic differentiation . Third, OIM-C-MSC transplantation can provide abundant COL1, which has been recognized as an indispensable ECM protein for new bone formation, at a bone defect site . Finally, a positive feedback loop involving COL1 deposition and YAP/TAZ activation may accelerate the bone regenerative properties of OIM-C-MSCs after transplantation. A future study investigating these molecular mechanisms in vivo may provide additional support for novel bone regenerative cell therapies using 3D-cultured C-MSCs.
In this present study, we mainly focused on the cellular property in 5-day OIM-treated C-MSCs. Because the 10-day or 15-day OIM-treated C-MSCs failed to induce bone regeneration in vivo [4, 6]. Interestingly, OIM treatment for more than 10 days induced mineralization, though profound cell apoptosis was also observed in C-MSCs [4, 6]. These findings suggested that excess osteoinduction in vitro may induce C-MSCs to become cellular calcific substances, not biological bone-like tissue. Although the precise molecular mechanism is unclear, mineral deposition may be toxic to the cells in the floating condition which decreased YAP/TAZ activity. To develop the culture protocol that can abrogate the mineral deposition-induced cell apoptosis in floating condition will provide us the biological bone-like tissue in vitro by using C-MSCs.
This present study clearly demonstrated the distinction of biological capacities between C-MSCs and OIM-C-MSCs in the context of mechanobiology. Briefly, 3D-cultured C-MSCs in floating conditions lost their actin cytoskeleton and had decreased YAP/TAZ activity, which directed cells to undergo adipo-/chondrogenesis. In contrast, OIM treatment facilitated COL1 deposition, which stimulated Intβ1-ROCK-F-actin-YAP/TAZ signaling to induce osteogenesis in C-MSCs. Importantly, the mechanotransduction cascade induced by OIM generated a positive feedback loop of YAP/TAZ activity in C-MSCs. These findings suggest that OIM-C-MSCs, which form a microenvironment that maintains high YAP/TAZ activity, are a superior candidate cell type for bone regenerative cell therapy.
We thank Daniel Mrozek who provided English language editing services on behalf of Medical English Service (Kyoto, Japan).
This work was supported by JSPS KAKENHI Grant Numbers JP18H02977, JP17K173510A, and JP17H06897 and a Research Grant from The Nakatomi Foundation and Mitsui Sumitomo Insurance Welfare Foundation.
Availability of data and materials
The datasets used or analyzed during the current study available from the corresponding author on reasonable request.
NK contributed to the study conception and design, collection and assembly of data, data analysis and interpretation, manuscript writing, and final approval of manuscript. MK contributed to the study conception and design, financial support, collection and assembly of data, data analysis and interpretation, manuscript writing, and final approval of manuscript. SM, MT, SH, TI, and KO contributed to the collection and assembly of data and final approval of manuscript. KT, SM, and TF contributed to the provision of study material, data analysis and interpretation, and final approval of manuscript. HK contributed to the study conception and design, financial support, administrative support, manuscript writing, and final approval of manuscript.
Ethics approval and consent to participate
Ethical approval for human subjects was obtained from the Independent Ethics Committee of Hiroshima University (reference number 422-2).
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