Cardiomyocytes fuse with surrounding noncardiomyocytes and reenter the cell cycle

被引:100
作者
Matsuura, K
Wada, H
Nagai, T
Iijima, Y
Minamino, T
Sano, M
Akazawa, H
Molkentin, JD
Kasanuki, H
Komuro, I [1 ]
机构
[1] Chiba Univ, Grad Sch Med, Dept Cardiovasc Sci & Med, Chiba 2608670, Japan
[2] Tokyo Womens Med Univ, Heart Inst Japan, Dept Cardiol, Tokyo 1628666, Japan
[3] Childrens Hosp, Med Ctr, Dept Pediat, Div Mol Cardiovasc Biol, Cincinnati, OH 45229 USA
关键词
D O I
10.1083/jcb.200312111
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The concept of the plasticity or transdifferentiation of adult stem cells has been challenged by the phenomenon of cell fusion. In this work, we examined whether neonatal cardiomyocytes fuse with various somatic cells including endothelial cells, cardiac fibroblasts, bone marrow cells and endothelial progenitor cells spontaneously in vitro. When cardiomyocytes were cocultured with endothelial cells or cardiac fibroblasts, they fused and showed phenotypes of cardiomyocytes. Furthermore, cardiomyocytes reentered the G2-M phase in the cell cycle after fusing with proliferative noncardiomyocytes. Transplanted endothelial cells or skeletal muscle-derived cells fused with adult cardiomyocytes in vivo. In the cryo-injured heart, there were Ki67-positive cells that expressed both cardiac and endothelial lineage marker proteins. These results suggest that cardiomyocytes fuse with other cells and enter the cell cycle by maintaining their phenotypes.
引用
收藏
页码:351 / 363
页数:13
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[1]   Adenoviral delivery of E2F-1 directs cell cycle reentry and p53-independent apoptosis in postmitotic adult myocardium in vivo [J].
Agah, R ;
Kirshenbaum, LA ;
Abdellatif, M ;
Truong, LD ;
Chakraborty, S ;
Michael, LH ;
Schneider, MD .
JOURNAL OF CLINICAL INVESTIGATION, 1997, 100 (11) :2722-2728
[2]   Fusion of bone-marrow-derived cells with Purkinje neurons, cardiomyocytes and hepatocytes [J].
Alvarez-Dolado, M ;
Pardal, R ;
Garcia-Vardugo, JM ;
Fike, JR ;
Lee, HO ;
Pfeffer, K ;
Lois, C ;
Morrison, SJ ;
Alvarez-Buylla, A .
NATURE, 2003, 425 (6961) :968-973
[3]   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
[4]   Reversibility of the differentiated state in somatic cells [J].
Baron, Margaret H. .
CURRENT OPINION IN CELL BIOLOGY, 1993, 5 (06) :1050-1056
[5]   Evidence that human cardiac myocytes divide after myocardial infarction (Publication with Expression of Concern. See vol. 379, pg. 1870, 2018) [J].
Beltrami, AP ;
Urbanek, K ;
Kajstura, J ;
Yan, SM ;
Finato, N ;
Bussani, R ;
Nadal-Ginard, B ;
Silvestri, F ;
Leri, A ;
Beltrami, CA ;
Anversa, P .
NEW ENGLAND JOURNAL OF MEDICINE, 2001, 344 (23) :1750-1757
[6]   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
[7]   G1 and G2 cell-cycle arrest following microtubule depolymerization in human breast cancer cells [J].
Blajeski, AL ;
Phan, VA ;
Kottke, TJ ;
Kaufmann, SH .
JOURNAL OF CLINICAL INVESTIGATION, 2002, 110 (01) :91-99
[8]   CYTOPLASMIC ACTIVATION OF HUMAN NUCLEAR GENES IN STABLE HETEROCARYONS [J].
BLAU, HM ;
CHIU, CP ;
WEBSTER, C .
CELL, 1983, 32 (04) :1171-1180
[9]   Plasticity of cell fate: Insights from heterokaryons [J].
Blau, HM ;
Blakely, BT .
SEMINARS IN CELL & DEVELOPMENTAL BIOLOGY, 1999, 10 (03) :267-272
[10]   CARDIAC-MUSCLE DISEASES IN GENETICALLY-ENGINEERED MICE - EVOLUTION OF MOLECULAR PHYSIOLOGY [J].
CHIEN, KR .
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 1995, 269 (03) :H755-H766