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A Microenvironment, Rather than Chemical, Initiates the Cardiomyogenic Differentiation of Marrow Stromal Cells

A Microenvironment, Rather than Chemical, Initiates the Cardiomyogenic Differentiation of Marrow Stromal Cells
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摘要 To investigate the potential of cardiomyogenic differentiation of rat bone marrow stromal cells (MSCs), they were exposed to 5-azacytidine tretments (single/repeat) at varying concentrations (3, 5, 10 μmol/L) and the fates of the cells were analyzed by immunocytochemistry, Western blot and the reporter gene of enhanced cyan fluorescent protein (ECFP) under the control of ventricular myosin light chain 2 (MLC2v) promoter. MSCs were also cocultured with cardiomyocytes for periods up to 16 days, the expression of cardiac myosin heavy chain (MHC) and troponin I (Tn I) proteins was analyzed. After the induction with 5-azacytidine, neither spontaneously beating cells nor myotubes were found; MHC and Tn I proteins were also undetectable and no ECFP-positive MSCs were detected. But when cocultured with cardiomyocytes, spontaneously contracting MSCs were observed and cardiac specific proteins could be detected. The results proved that the novel effects of 5-azacytidine on the cardiomyogenic differentiation of MSCs should be questioned and a direct intercellular communication with cardiomyocytes is necessary for MSCs to differentiate into cardiomyocytes. Key words cardiomyocyte - cell differentiation - stem cell CLC number Q 813.5 - R 542.2+2 Foundation item: Supported by the Natural Science Foundation of Hubei Province (2002AB00150)Biography: LIU Wei-xin (1976-), male, Ph. D candidate, research direction: stem cell and cellular biology. To investigate the potential of cardiomyogenic differentiation of rat bone marrow stromal cells (MSCs), they were exposed to 5-azacytidine tretments (single/repeat) at varying concentrations (3, 5, 10 μmol/L) and the fates of the cells were analyzed by immunocytochemistry, Western blot and the reporter gene of enhanced cyan fluorescent protein (ECFP) under the control of ventricular myosin light chain 2 (MLC2v) promoter. MSCs were also cocultured with cardiomyocytes for periods up to 16 days, the expression of cardiac myosin heavy chain (MHC) and troponin I (Tn I) proteins was analyzed. After the induction with 5-azacytidine, neither spontaneously beating cells nor myotubes were found; MHC and Tn I proteins were also undetectable and no ECFP-positive MSCs were detected. But when cocultured with cardiomyocytes, spontaneously contracting MSCs were observed and cardiac specific proteins could be detected. The results proved that the novel effects of 5-azacytidine on the cardiomyogenic differentiation of MSCs should be questioned and a direct intercellular communication with cardiomyocytes is necessary for MSCs to differentiate into cardiomyocytes. Key words cardiomyocyte - cell differentiation - stem cell CLC number Q 813.5 - R 542.2+2 Foundation item: Supported by the Natural Science Foundation of Hubei Province (2002AB00150)Biography: LIU Wei-xin (1976-), male, Ph. D candidate, research direction: stem cell and cellular biology.
出处 《Wuhan University Journal of Natural Sciences》 CAS 2004年第4期513-521,共9页 武汉大学学报(自然科学英文版)
基金 SupportedbytheNaturalScienceFoundationofHubeiProvince(2 0 0 2AB0 0 1 50 )
关键词 CARDIOMYOCYTE cell differentiation stem cell cardiomyocyte cell differentiation stem cell
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参考文献11

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