Culturing of bone marrow cells in serum-free RPMI-1640 medium led to a decrease in the rate of DNA biosynthesis. Addition of HDL or their main protein component apolipoprotein A-I to the culture medium dose-dependently increased the rate of [3H]-thymidine incorporation into DNA. The maximum stimulation was achieved at HDL concentration of 80 μg/ml and apolipoprotein A-I concentration of 20 μg/ml. To identify the target-cells of apolipoprotein A-I, we used thymidine analogue 5-ethynyl-2’-deoxyuridine (EdU) that incorporates into cell DNA at the stage of replicative DNA synthesis (S phase) and can be detected by fluorescence microscopy. In bone marrow cell culture, apolipoprotein A-I stimulates the proliferation of monocyte (monoblasts, promonocytes) and granulocyte (myeloblasts, promyelocytes) progenitor cells, as well as bone marrow stromal cells.
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References
Goldberg ED, Dygai AM, Shakhov VP. Methods of Tissue Culture in Hematology. Tomsk, 1992. Russian.
Panin LE, Khar’kovskii AV, Usynin IF, Tuzikov FV, Tuzikova NA. Effect of tetrahydrocortisol-apolipoprotein A-I complex on protein biosynthesis in hepatocytes and on the secondary structure of eukaryotic DNA. Mol. Biol. 1999;33(4):596-601.
Panin LE, Usynin IF, Khar’kovskii AB, Poteryaeva ON. Effect of high-density lipoproteins and hydrocortisone on apolipoprotein E production in Kupffer cells. Bull. Exp. Biol. Med. 1998;126(1): 679-680.
Panin LE, Khoshchenko OM, Usynin IF. Role of apolipoprotein A-I in steroid-induced activation of DNA and protein synthesis in hepatocytes. Bull. Exp. Biol. Med. 2001;131(1): 50-52.
Pykhtina MB, Ivanov ID, Beklemishev AB. Development of effective ways of apolipoprotein A-I isolation from human plasma. Biofarmatsevt. Zh. 2012;4(6):37-45. Russian.
Andrew SM, Titus JA. Purification of immunoglobulin G. Curr. Protoc. Cell Biol. 2001. Chapter 16; Unit 16.3. doi: https://doi.org/10.1002/0471143030.cb1603s05.
Bolliger АP. Cytologic evaluation of bone marrow in rats: indications, methods, and normal morphology. Vet. Clin. Pathol. 2004;33(2):58-67.
Cham BE, Knowles BR. A solvent system for delipidation of plasma or serum without protein precipitation. J. Lipid Res. 1976;17(2):176-181.
Gordon SM, Hofmann S, Askew DS, Davidson WS. High density lipoprotein: it’s not just about lipid transport anymore. Trends Endocrinol. Metab. 2011;22(1):9-15.
Handwerger S, Myers S, Richards R, Richardson B, Turzai L, Moeykins C, Meyer T, Anantharamahiah G.M. Apolipoprotein A-I stimulates placental lactogen expression by human trophoblast cells. Endocrinology. 1995;136(12):5555-5560.
Jin X, Xu Q, Champion K, Kruth HS. Endotoxin contamination of apolipoprotein A-I: effect on macrophage proliferation — a cautionary tale. Atherosclerosis. 2015;240(1):121-124.
Mills GL, Lane PA, Weech PK. The isolation and purification of plasma lipoproteins. Laboratory Techniques in Biochemistry and Molecular Biology: a Guidebook to Lipoprotein Technique. Burdon RH, Knippenberg PH, eds. Amsterdam, 1984. P. 18-116.
Nofer JR. Signal transduction by HDL: agonists, receptors, and signaling cascades. Handb. Exp. Pharmacol. 2015;224:229-256.
Yamato K, Tamasawa N, Murakami H, Matsui J, Tanabe J, Suda T, Yasujima M. Evaluation of apolipoprotein E secretion by macrophages in type 2 diabetic patients: role of HDL and apolipoprotein A-I. Diabetes Res. Clin. Pract. 2005;69(2):124-128.
Zhou X, von Eckardstein A. Effect of HDL and apoAI on PGE2 production by monocyte-derived macrophages. J. Huazhong. Univ. Sci. Technolog. Med. Sci. 2002;22(4):270-272.
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Translated from Byulleten’ Eksperimental’noi Biologii i Meditsiny, Vol. 164, No. 9, pp. 285-288, September, 2017
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Usynin, I.F., Dudarev, A.N., Gorodetskaya, A.Y. et al. Apolipoprotein A-I Stimulates Cell Proliferation in Bone Marrow Cell Culture. Bull Exp Biol Med 164, 308–311 (2018). https://doi.org/10.1007/s10517-018-3978-0
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DOI: https://doi.org/10.1007/s10517-018-3978-0