Bone Marrow Mesenchymal Stem Cells Stimulate Cardiac Stem Cell Proliferation and Differentiation

被引:591
作者
Hatzistergos, Konstantinos E. [1 ]
Quevedo, Henry [1 ]
Oskouei, Behzad N. [1 ]
Hu, Qinghua [1 ,2 ]
Feigenbaum, Gary S. [1 ]
Margitich, Irene S. [1 ]
Mazhari, Ramesh [3 ]
Boyle, Andrew J. [4 ]
Zambrano, Juan P. [1 ,2 ]
Rodriguez, Jose E. [1 ]
Dulce, Raul [1 ]
Pattany, Pradip M. [1 ]
Valdes, David [1 ]
Revilla, Concepcion [5 ]
Heldman, Alan W. [1 ,2 ]
McNiece, Ian [1 ,2 ]
Hare, Joshua M. [1 ,2 ]
机构
[1] Leonard M Miller Sch Med, Interdisciplinary Stem Cell Inst, Miami, FL USA
[2] Leonard M Miller Sch Med, Div Cardiovasc, Dept Med, Miami, FL USA
[3] George Washington Univ, Div Cardiol, Washington, DC USA
[4] Univ Calif San Francisco, Dept Med, Div Cardiol, UCSF Heart & Vasc Ctr, San Francisco, CA 94143 USA
[5] Inst Nacl Invest & Tecnol Agr & Alimentaria, Dpto Biotecnol, Madrid, Spain
关键词
myocardial infarction; mesenchymal stem cells; cardiac stem cells; myocardial regeneration; CHRONIC ISCHEMIC CARDIOMYOPATHY; ZEBRAFISH HEART REGENERATION; ACUTE MYOCARDIAL-INFARCTION; PROGENITOR CELLS; IN-VIVO; SMOOTH-MUSCLE; EX-VIVO; REPAIR; THERAPY; CARDIOMYOCYTES;
D O I
10.1161/CIRCRESAHA.110.222703
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Rationale: The regenerative potential of the heart is insufficient to fully restore functioning myocardium after injury, motivating the quest for a cell-based replacement strategy. Bone marrow-derived mesenchymal stem cells (MSCs) have the capacity for cardiac repair that appears to exceed their capacity for differentiation into cardiac myocytes. Objective: Here, we test the hypothesis that bone marrow derived MSCs stimulate the proliferation and differentiation of endogenous cardiac stem cells (CSCs) as part of their regenerative repertoire. Methods And Results: Female Yorkshire pigs (n = 31) underwent experimental myocardial infarction (MI), and 3 days later, received transendocardial injections of allogeneic male bone marrow-derived MSCs, MSC concentrated conditioned medium (CCM), or placebo (Plasmalyte). A no-injection control group was also studied. MSCs engrafted and differentiated into cardiomyocytes and vascular structures. In addition, endogenous c-kit(+) CSCs increased 20-fold in MSC-treated animals versus controls (P<0.001), there was a 6-fold increase in GATA-4(+) CSCs in MSC versus control (P<0.001), and mitotic myocytes increased 4-fold (P=0.005). Porcine endomyocardial biopsies were harvested and plated as organotypic cultures in the presence or absence of MSC feeder layers. In vitro, MSCs stimulated c-kit(+) CSCs proliferation into enriched populations of adult cardioblasts that expressed Nkx2-5 and troponin I. Conclusions: MSCs stimulate host CSCs, a new mechanism of action underlying successful cell-based therapeutics. (Circ Res. 2010;107:913-922.)
引用
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页码:913 / +
页数:33
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