Cardiomyogenic Potential of C-Kit+-Expressing Cells Derived From Neonatal and Adult Mouse Hearts

被引:176
作者
Zaruba, Marc-Michael [1 ,2 ,3 ]
Soonpaa, Mark [1 ,2 ]
Reuter, Sean [1 ,2 ]
Field, Loren J. [1 ,2 ]
机构
[1] Indiana Univ, Sch Med, Riley Heart Res Ctr, Herman B Wells Ctr Pediat Res, Indianapolis, IN 46202 USA
[2] Indiana Univ, Sch Med, Krannert Inst Cardiol, Indianapolis, IN 46202 USA
[3] Univ Munich, Klinikum Grosshadern, Dept Med 1, D-8000 Munich, Germany
基金
美国国家卫生研究院;
关键词
progenitor cells; molecular biology; myocardial infarction; myocytes; cardiac; stem cells; CARDIAC STEM-CELLS; C-KIT; PROGENITOR CELLS; MYOCARDIAL-INFARCTION; PRECURSOR CELLS; BONE-MARROW; MULTIPOTENT; DIFFERENTIATION; CARDIOMYOCYTES; IDENTIFICATION;
D O I
10.1161/CIRCULATIONAHA.109.909093
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background-C-kit is a receptor tyrosine kinase family member expressed in hematopoietic stem cells. C-kit is also transiently expressed in cardiomyocyte precursors during development and in a rare cell population in the normal adult heart. In the present study, the cardiomyogenic potential of c-kit(+) cells isolated from normal neonatal, normal adult, and infarcted adult mouse hearts was evaluated. Methods and Results-Magnetic activated cell sorting was used to prepare c-kit(+) cells from the hearts of ACT-EGFP/MHC-nLAC double transgenic mice. These animals exhibit widespread enhanced green fluorescent protein (EGFP) expression and cardiomyocyte-restricted nuclear beta-galactosidase activity, thus permitting simultaneous tracking of cell survival and differentiation. A subset of the c-kit(+) cells from double transgenic neonatal hearts acquired a cardiomyogenic phenotype when cocultured with fetal cardiomyocytes (2.4% of all EGFP(+) cells screened) but rarely when cultured alone or when cocultured with mouse fibroblasts (0.03% and 0.05% of the EGFP(+) cells screened, respectively). In contrast, c-kit(+) cells from normal adult double transgenic hearts failed to undergo cardiomyogenic differentiation when cocultured with nontransgenic fetal cardiomyocytes (>18 000 EGFP(+) cells screened) or when transplanted into normal or infarcted adult mouse hearts (14 EGFP(+) grafts examined). A single c-kit(+) cell from an infarcted double transgenic adult heart was observed to acquire a cardiomyogenic phenotype in coculture (>37 000 EGFP(+) cells screened). Conclusions-These data suggest that the ability of cardiac-resident c-kit(+) cells to acquire a cardiomyogenic phenotype is subject to temporal limitations or, alternatively, that the cardiomyogenic population is lost. Elucidation of the underlying molecular basis may permit robust cardiomyogenic induction in adult-derived cardiac c-kit(+) cells. (Circulation. 2010;121:1992-2000.)
引用
收藏
页码:1992 / U56
页数:33
相关论文
共 32 条
[1]   Transdifferentiation of blood-derived human adult endothelial progenitor cells into functionally active cardiomyocytes [J].
Badorff, C ;
Brandes, RP ;
Popp, R ;
Rupp, S ;
Urbich, C ;
Aicher, A ;
Fleming, I ;
Busse, R ;
Zeiher, A ;
Dimmeler, S .
CIRCULATION, 2003, 107 (07) :1024-1032
[2]   Human cardiac stem cells [J].
Bearzi, Claudia ;
Rota, Marcello ;
Hosoda, Toru ;
Tillmanns, Jochen ;
Nascirnbene, Angelo ;
De Angelis, Antonella ;
Yasuzawa-Amano, Saori ;
Trofimova, Irina ;
Siggins, Robert W. ;
LeCapitaine, Nicole ;
Cascapera, Stefano ;
Beltrami, Antonio P. ;
D'Alessandro, David A. ;
Zias, Elias ;
Quaini, Federico ;
Urbanek, Konrad ;
Michler, Robert E. ;
Bolli, Roberto ;
Kajstura, Jan ;
Leri, Annarosa ;
Anversa, Piero .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2007, 104 (35) :14068-14073
[3]   Adult cardiac stem cells are multipotent and support myocardial regeneration [J].
Beltrami, AP ;
Barlucchi, L ;
Torella, D ;
Baker, M ;
Limana, F ;
Chimenti, S ;
Kasahara, H ;
Rota, M ;
Musso, E ;
Urbanek, K ;
Leri, A ;
Kajstura, J ;
Nadal-Ginard, B ;
Anversa, P .
CELL, 2003, 114 (06) :763-776
[4]   Evidence for Cardiomyocyte Renewal in Humans [J].
Bergmann, Olaf ;
Bhardwaj, Ratan D. ;
Bernard, Samuel ;
Zdunek, Sofia ;
Barnabe-Heider, Fanie ;
Walsh, Stuart ;
Zupicich, Joel ;
Alkass, Kanar ;
Buchholz, Bruce A. ;
Druid, Henrik ;
Jovinge, Stefan ;
Frisen, Jonas .
SCIENCE, 2009, 324 (5923) :98-102
[5]   Mouse ES cell-derived cardiac precursor cells are multipotent and facilitate identification of novel cardiac genes [J].
Christoforou, Nicolas ;
Miller, Ronald A. ;
Hill, Christine M. ;
Jie, Chunfa C. ;
McCallion, Andrew S. ;
Gearhart, John D. .
JOURNAL OF CLINICAL INVESTIGATION, 2008, 118 (03) :894-903
[6]   G-CSF administration after myocardial infarction in mice attenuates late ischemic cardiomyopathy by enhanced arteriogenesis [J].
Deindl, Elisabeth ;
Zaruba, Marc-Michael ;
Brunner, Stefan ;
Huber, Bruno ;
Mehl, Ursula ;
Assmann, Gerald ;
Hoefer, Imo E. ;
Mueller-Hoecker, Josef ;
Franz, Wolfgang-Michael .
FASEB JOURNAL, 2006, 20 (07) :956-+
[7]   c-Kit - A hematopoietic cell essential receptor tyrosine kinase [J].
Edling, Charlotte E. ;
Hallberg, Bengt .
INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY, 2007, 39 (11) :1995-1998
[8]   Cardioprotective c-kit+ cells are from the bone marrow and regulate the myocardial balance of angiogenic cytokines [J].
Fazel, Shafie ;
Cimini, Massimo ;
Chen, Liwen ;
Li, Shuhong ;
Angoulvant, Denis ;
Fedak, Paul ;
Verma, Subodh ;
Weisel, Richard D. ;
Keating, Armand ;
Li, Ren-Ke .
JOURNAL OF CLINICAL INVESTIGATION, 2006, 116 (07) :1865-1877
[9]   Evolution of the c-kit-positive cell response to pathological challenge in the myocardium [J].
Fransioli, Jenna ;
Bailey, Brandi ;
Gude, Natalie A. ;
Cottage, Christopher T. ;
Muraski, John A. ;
Emmanuel, Gregory ;
Wu, Weitao ;
Alvarez, Roberto ;
Rubio, Marta ;
Ottolenghi, Sergio ;
Schaefer, Erik ;
Sussman, Mark A. .
STEM CELLS, 2008, 26 (05) :1315-1324
[10]   Akt promotes increased cardiomyocyte cycling and expansion of the cardiac progenitor cell population [J].
Gude, Natalie ;
Muraski, John ;
Rubio, Marta ;
Kajstura, Jan ;
Schaefer, Erik ;
Anversa, Piero ;
Sussman, Mark A. .
CIRCULATION RESEARCH, 2006, 99 (04) :381-388