Imaging Survival and Function of Transplanted Cardiac Resident Stem Cells

被引:163
作者
Li, Zongjin [1 ,2 ]
Lee, Andrew [1 ,2 ]
Huang, Mei [1 ,2 ]
Chun, Hyung [3 ]
Chung, Jaehoon [3 ]
Chu, Pauline [5 ]
Hoyt, Grant [4 ]
Yang, Phillip [3 ]
Rosenberg, Jarrett [1 ,2 ]
Robbins, Robert C. [4 ]
Wu, Joseph C. [1 ,2 ,3 ]
机构
[1] Stanford Univ, Sch Med, Dept Radiol, Stanford, CA 94305 USA
[2] Stanford Univ, Sch Med, Mol Imaging Program MIPS0, Stanford, CA 94305 USA
[3] Stanford Univ, Sch Med, Dept Med, Div Cardiol, Stanford, CA 94305 USA
[4] Stanford Univ, Sch Med, Dept Cardiothorac Surg, Stanford, CA 94305 USA
[5] Stanford Univ, Sch Med, Dept Comparat Med, Stanford, CA 94305 USA
关键词
molecular imaging; cardiac stem cells; ischemic heart disease; differentiation; cell fate; PROGENITOR CELLS; IN-VITRO; HEART; DIFFERENTIATION; REGENERATION; MYOCARDIUM; THERAPY;
D O I
10.1016/j.jacc.2008.12.036
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
Objectives The goal of this study is to characterize resident cardiac stem cells (CSCs) and investigate their therapeutic efficacy in myocardial infarction by molecular imaging methods. Background CSCs have been isolated and characterized in vitro. These cells offer a provocative method to regenerate the damaged myocardium. However, the survival kinetics and function of transplanted CSCs have not been fully elucidated. Methods CSCs were isolated from L2G85 transgenic mice (FVB strain background) that constitutively express both firefly luciferase and enhanced green fluorescence protein reporter gene. CSCs were characterized in vitro and transplanted in vivo into murine infarction models. Multimodality noninvasive imaging techniques were used to assess CSC survival and therapeutic efficacy for restoration of cardiac function. Results CSCs can be isolated from L2G85 mice, and fluorescence-activated cell sorting analysis showed expression of resident CSC markers (Sca-1, c-Kit) and mesenchymal stem cell markers (CD90, CD106). Afterwards, 5 x 10(5) CSCs (n = 30) or phosphate-buffered saline control (n = 15) was injected into the hearts of syngeneic FVB mice undergoing left anterior descending artery ligation. Bioluminescence imaging showed poor donor cell survival by week 8. Echocardiogram, invasive hemodynamic pressure-volume analysis, positron emission tomography imaging with fluorine-18-fluorodeoxyglucose, and cardiac magnetic resonance imaging demonstrated no significant difference in cardiac contractility and viability between the CSC and control group. Finally, postmortem analysis confirmed transplanted CSCs integrated with host cardiomyocytes by immunohistology. Conclusions In a mouse myocardial infarction model, Sca-1-positive CSCs provide no long-term engraftment and benefit to cardiac function as determined by multimodality imaging. (J Am Coll Cardiol 2009;53:1229-40) (C) 2009 by the American College of Cardiology Foundation
引用
收藏
页码:1229 / 1240
页数:12
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