Optimal concentration of 1,25-vitamin-D3 to induce the differentiation of bone marrow mesenchymal stem cells into cardiomyocyte-like cells in vitro

LIU Yang Lü Yang WANG Hao-yu LI Jiao REN Jun-xu WANG Hai-ping

Acta Anatomica Sinica ›› 2019, Vol. 50 ›› Issue (5) : 580-588.

PDF(1282 KB)
Welcome to visit Acta Anatomica Sinica! Today is Chinese
PDF(1282 KB)
Acta Anatomica Sinica ›› 2019, Vol. 50 ›› Issue (5) : 580-588. DOI: 10.16098/j.issn.0529-1356.2019.05.007

Optimal concentration of 1,25-vitamin-D3 to induce the differentiation of bone marrow mesenchymal stem cells into cardiomyocyte-like cells in vitro

  • LIU Yang Lü Yang WANG Hao-yu LI Jiao REN Jun-xu WANG Hai-ping*
Author information +
History +

Abstract

Objective To explore the optimal concentration of 1,25-vitamin-D3 for inducing the differentiation of bone marrow mesenchymal stem cells (BMSCs) into cardiomyocyte-like cells in vitro. Methods BMSCs of SD rats were isolated and cultured by whole bone marrow adherent method combined with density gradient centrifugations. Depending on the final concentration of 1,25-vitamin-D3, the 2nd-generation BMSCs were divided into five groups: 3 nmol/L group, 6 nmol/L group, 12 nmol/L group, 24 nmol/L group and the control group. The adherent cells were observed dynamically under the inverted phase contrast microscope, including their morphology and growth status. The surface antigens, morphological characteristics, protein expression and mRNA expression of the cells in each group were assessed. Results 1. Under the inverted phase contrast microscope, most of the primary cells showed a short spindle shape after 72 hours of culture. After 1 week of culture, the cells showed diversified morphology. The adjacent cells of BMSCs, induced after 4 weeks, were closely connected with each other, and the arrangement had obvious directivity. There were differences in the number and morphology of BMSCs, induced by 1,25-vitamin-D3 at different concentrations. 2. The result of flow cytometry showed that the positive expression rates of CD29, CD45 and CD90 were 97.4%, 3.3% and 91.4%, respectively, 3. The results of immunofluorescence, immunocytochemistry and Western blotting revealed that the expressions of tropomyosin(TPM), connexin43(Cx43) and cardiac troponin T(cTnT) in 6 nmol/L group were significantly higher than that of the other groups, while that in control group were weak or negative (P<0.05). 4. Transmission electron microscope(TEM) observation showed that the induced cells had a cardiomyocyte-like ultra structure: there were many parallel arranged myofilaments, mitochondria, ribosomes, rough endoplasmic reticulum and other organelles in the cytoplasm. 5. The result of Real-time PCR showed that the induced cells could express GATA binding protein 4(GATA 4) and Nkx2.5 at the 1st week, and then the expression of them decreased at the 2nd week, but then increased at the 4th week. The 6 nmol/L group was superior to the other three groups in gene expression (P<0.05). Conclusion 1,25-vitamin-D3 can induce BMSCs to obtain myocardial differentiation phenotype, and the optimum concentration of inducing differentiation is 6 nmol/L.

Key words

Bone marrow mesenchymal stem cell / 1,25-vitamin-D3 / Cardiomyocyte-like cell / Cell differentiation / Western blotting / Rat

Cite this article

Download Citations
LIU Yang Lü Yang WANG Hao-yu LI Jiao REN Jun-xu WANG Hai-ping.
Optimal concentration of 1,25-vitamin-D3 to induce the differentiation of bone marrow mesenchymal stem cells into cardiomyocyte-like cells in vitro
[J]. Acta Anatomica Sinica. 2019, 50(5): 580-588 https://doi.org/10.16098/j.issn.0529-1356.2019.05.007

References

 [1] Lü Y,  Liu B, Liu Y, et al. TGF-β1 combined with Sal-B promotes cardiomyocyte differentiation of rat mesenchymal stem cells[J]. Exp Ther Med, 2018, 15(6): 5359-5364.
 [2] Shen X, Pan B, Zhou H, et al. Differentiation of mesenchymal stem cells into cardiomyocytes is regulated by miRNA-1-2 via WNT signaling pathway[J]. J Biomed Sci, 2017, 24(1): 29.
 [3] Chen Y, Wang C, Huang Q, et al. Caveolin-1 plays an important role in the differentiation of bone marrow-derived mesenchymal stem cells into cardiomyocytes[J]. Cardiology, 2017, 136(1): 40-48.
 [4] Lü Y, Liu B, Wang HP, et al. Transforming growth factor-β1 combined with tanshinoneⅡA induces bone marrow mesenchymal stem cells differentiating into cardiomyocyte-like cells in vitro[J]. Acta Anatomica Sinica, 2016, 47(5): 620-627. (in Chinese)
吕洋, 刘博, 王海萍, 等. 转化生长因子β1和丹参酮ⅡA联合诱导骨髓间充质干细胞向心肌样细胞的分化[J]. 解剖学报, 2016, 47(5): 620-627.
 [5] Hlaing SM, Garcia LA, Contreras JR, et al.1,25-vitamin D3 promotes cardiac differentiation through modulation of theWnt signaling pathway[J]. J Mol Endocrinol, 2014, 53(3):303-317. 
 [6] Richart T, Li Y, Staessen JA. Renal versus extrarenal activation of vitamin D in relation to atherosclerosis, arterial stiffening, and hypertension[J]. Am J Hypertens, 2007, 20(9):1007-1015.
 [7] Zerwekh JE. Blood biomarkers of vitamin D status[J]. Am J Clin Nutr, 2008, 87(4):1087S-1091S.
 [8] Prietl B, Treiber G, Pieber TR, et al.Vitamin D and immune function[J]. Nutrients, 2013, 5(7):2502-2521.
 [9] Stivelman E, Retnakaran R. Role of vitamin D in the pathophysiology and treatment of type 2 diabetes[J]. Curr Diabetes Rev, 2012, 8(1):42-47.
 [10]Gardner DG,Chen S,Glenn DJ. Vitamin D and the heart[J]. Am J Physiol Regul Integr Comp Physiol,2013, 305(9):R969-977.
 [11]Nibbelink KA, Tishkoff DX, Hershey SD, et al.1,25(OH)2 vitamin D3 actions on cell proliferation, size, gene expression, and receptor localization, in the HL-1 cardiac myocyte[J]. J Steroid Biochem Mol Biol, 2007, 103(3-5):533-537.
 [12]O’Connell TD, Berry JE, Jarvis AK, et al.1,25-dihydroxyvitamin D3 regulation of cardiac myocyte proliferation and hypertrophy[J]. Am J Physiol, 1997, 272(4 Pt 2):H1751-1758.
 [13]Kim IM, Norris KC, Artaza JN. Vitamin D and cardiac differentiation[J]. Vitam Horm, 2016, 100:299-320.
 [14]Lehrer SS, Geeves MA. The myosin-activated thin filament regulatory state, M–-open:a link to hypertrophic cardiomyopathy (HCM) [J]. J Muscle Res Cell Motil, 2014, 35(2):153-160. 
 [15]Gunning P, O’Neill G, Hardeman E. Tropomyosin-based regulation of the actin cytoskeleton in time and space[J]. Physiol Rev, 2008, 88(1):1-35. 
 [16]Ruscic KJ, Miceli F, Villalba-Galea CA, et al. IKs channels open slowly because KCNE1 accessory subunits slow the movement of S4 voltage sensors in KCNQ1 pore-forming subunits[J]. Proc Natl Acad Sci USA, 2013, 110(7):E559-566.
 [17]Li N, Hou XL. Differentiation of human bone marrow mesenchymal stem cells into cardiomyocyte like cells[J]. Chinese Journal of Clinical Pharmacology and Therapeutics, 2007, 12(4):401-404. (in Chinese)
李宁,侯相麟. 人骨髓间充质干细胞分化为心肌样细胞的研究[J]. 中国临床药理学与治疗学,2007,12(4):401-404.
 [18]Zhang J, Xiong J. Advances in clinical application of cardiac troponin[J]. Chinese Journal of Cardiovascular Rehabilitation Medicine, 2018, 27(3):360-364. (in Chinese)
张敬, 熊娟. 心肌肌钙蛋白的临床应用进展[J]. 心血管康复医学杂志, 2018, 27(3):360-364.
 [19]Zhang X, Wang J, Wang B, et al.A novel missense mutation of GATA4 in a Chinese family with congenital heart disease[J]. PLoS One, 2016, 11(7):e0158904.
 [20]Kasahara H, Bartunkova S, Schinke M, et al.Cardiac and extracardiac expression of Csx/Nkx2.5 homeodomain protein[J]. Circ Res, 1998, 82(9):936-946. 
Optimal concentration of 1,25-vitamin-D3 to induce the differentiation of bone marrow mesenchymal stem cells into cardiomyocyte-like cells in vitro
" title="Share on Weibo" target="_blank">
PDF(1282 KB)

Accesses

Citation

Detail

Sections
Recommended

/