Stem Cell Factor Gene Transfer Promotes Cardiac Repair After Myocardial Infarction via In Situ Recruitment and Expansion of c-kit(+) Cells

作者：Yaniz Galende Elisa; Chen Jiqiu; Chemaly Elie; Liang Lifan; Hulot Jean Sebastien; McCollum LaTronya; Arias Teresa; Fuster Valentin; Zsebo Krisztina M; Hajjar Roger J^*

来源：Circulation Research, 2012, 111(11): 1434-U188.

DOI：10.1161/CIRCRESAHA.111.263830

• cardiac myocyte regeneration
• gene transfer
• myocardial infarction
• stem cell factor

Rationale: There is growing evidence that the myocardium responds to injury by recruiting c-kit(+) cardiac progenitor cells to the damage tissue. Even though the ability of exogenously introducing c-kit(+) cells to injured myocardium has been established, the capability of recruiting these cells through modulation of local signaling pathways by gene transfer has not been tested.
Objective: To determine whether stem cell factor gene transfer mediates cardiac regeneration in a rat myocardial infarction model, through survival and recruitment of c-kit(+) progenitors and cell-cycle activation in cardiomyocytes, and explore the mechanisms involved.
Methods and Results: Infarct size, cardiac function, cardiac progenitor cells recruitment, fibrosis, and cardiomyocyte cell-cycle activation were measured at different time points in controls (n=10) and upon stem cell factor gene transfer (n=13) after myocardial infarction. We found a regenerative response because of stem cell factor overexpression characterized by an enhancement in cardiac hemodynamic function: an improvement in survival; a reduction in fibrosis, infarct size and apoptosis; an increase in cardiac c-kit(+) progenitor cells recruitment to the injured area; an increase in cardiomyocyte cell-cycle activation; and Wnt/beta-catenin pathway induction.
Conclusions: Stem cell factor gene transfer induces c-kit(+) stem/progenitor cell expansion in situ and cardiomyocyte proliferation, which may represent a new therapeutic strategy to reverse adverse remodeling after myocardial infarction. (Circ Res. 2012;111:1434-1445.)

• 出版日期2012-11-9