Stimulation of sphingosine-1-phosphate on cardiomyogenic differentiation of mesenchymal stem cells.
- Author:
Lili JIANG
;
Tianqing LIU
;
Kedong SONG
;
Shui GUAN
;
Xiangqin LI
;
Dan GE
- Publication Type:Journal Article
- MeSH:
Adipose Tissue;
cytology;
metabolism;
Cell Differentiation;
drug effects;
Cells, Cultured;
Culture Media;
Humans;
Lysophospholipids;
pharmacology;
Mesenchymal Stromal Cells;
cytology;
drug effects;
Myocytes, Cardiac;
cytology;
Sphingosine;
analogs & derivatives;
pharmacology;
Umbilical Cord;
cytology
- From:
Chinese Journal of Biotechnology
2013;29(11):1617-1628
- CountryChina
- Language:Chinese
-
Abstract:
To study the effect of sphingosine-1-phosphate (S1P) on the cardiomyogenic differentiation of human umbilical cord mesenchymal stem cells (UC-MSCs) and human adipose-derived mesenchymal stem cells (AD-MSCs), we seeded the cells in the culture plates and used cardiomyocyte culture medium (CMCM) combining with different concentration of S1P to induce UC-MSCs and AD-MSCs in vitro for 7, 14 and 28 days. Cardiomyogenic differentiations were identified through immunofluorescence staining, and the results were observed with fluorescence microscopy and confocal microscopy. The effects of S1P and CMCM on cell activity were evaluated by the methyl thiazolyl tetrazolium assay. The functional characteristic similar to cardiomyocytes was evaluated through detecting calcium transient. Our results showed that cardiomyogenic differentiation of UC-MSCs or AD-MSCs were enhanced with S1P concentration increasing, but cell activities declined. Results showed that the suitable differentiation time was 14 days, and the optimal concentration of S1P was 0.5 micromol/L. When working together with CMCM, S1P could promote the differentiation of UC-MSCs or AD-MSCs into functional cardiomyocytes, giving rise to specific electrophysiological properties (the calcium transient). Taken together, our results suggested that S1P could promote the differentiation of UC-MSCs or AD-MSCs into functional cardiomyocytes when being cultured in CMCM.
