Cardiac Transcription Factors Driven Lineage-Specification of Adult Stem Cells

被引:19
作者
Arminan, Ana [3 ]
Gandia, Carolina [3 ]
Manuel Garcia-Verdugo, Jose [2 ,3 ]
Lledo, Elisa [3 ]
Luis Mullor, Jose [3 ]
Anastasio Montero, Jose [3 ]
Sepulveda, Pilar [1 ,3 ]
机构
[1] Fdn Invest Hosp Univ la Fe, Regenerat Med & Heart Transplantat Unit, Valencia 46009, Spain
[2] Univ Valencia, Inst Cavanilles, Valencia, Spain
[3] Ctr Invest Principe Felipe, Valencia, Spain
关键词
Mesenchymal Stem Cells; Neonatal Rat Cardiomyocytes; Cardiac Specification; Cardiac Transcription Factors; MARROW STROMAL CELLS; BONE-MARROW; MYOCARDIAL-INFARCTION; PROGENITOR CELLS; GENE-EXPRESSION; IN-VITRO; CARDIOMYOCYTES; DIFFERENTIATION; HEART; GATA4;
D O I
10.1007/s12265-009-9144-3
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Differentiation of human bone marrow mesenchymal stem cells (hBMSC) into the cardiac lineage has been assayed using different approaches such as coculture with cardiac or embryonic cells, treatment with factors, or by seeding cells in organotypic cultures. In most cases, differentiation was evaluated in terms of expression of cardiac-specific markers at protein or molecular level, electrophysiological properties, and formation of sarcomers in differentiated cells. As observed in embryonic stem cells and cardiac progenitors, differentiation of MSC towards the cardiac lineage was preceded by translocation of NKX2.5 and GATA4 transcription factors to the nucleus. Here, we induce differentiation of hBMSC towards the cardiac lineage using coculture with neonatal rat cardiomyocytes. Although important ultrastructural changes occurred during the course of differentiation, sarcomerogenesis was not fully achieved even after long periods of time. Nevertheless, we show that the main cardiac markers, NKX2.5 and GATA4, translocate to the nucleus in a process characteristic of cardiac specification.
引用
收藏
页码:61 / 65
页数:5
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