Cardiac stem cells and mechanisms of myocardial regeneration

被引:311
作者
Leri, A [1 ]
Kajstura, J [1 ]
Anversa, P [1 ]
机构
[1] New York Med Coll, Cardiovasc Res Inst, Dept Med, Valhalla, NY 10595 USA
关键词
D O I
10.1152/physrev.00013.2005
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
This review discusses current understanding of the role that endogenous and exogenous progenitor cells may have in the treatment of the diseased heart. In the last several years, a major effort has been made in an attempt to identify immature cells capable of differentiating into cell lineages different from the organ of origin to be employed for the regeneration of the damaged heart. Embryonic stem cells (ESCs) and bone marrow-derived cells (BMCs) have been extensively studied and characterized, and dramatic advances have been made in the clinical application of BMCs in heart failure of ischemic and nonischemic origin. However, a controversy exists concerning the ability of BMCs to acquire cardiac cell lineages and reconstitute the myocardium lost after infarction. The recognition that the adult heart possesses a stem cell compartment that can regenerate myocytes and coronary vessels has raised the unique possibility to rebuild dead myocardium after infarction, to repopulate the hypertrophic decompensated heart with new better functioning myocytes and vascular structures, and, perhaps, to reverse ventricular dilation and wall thinning. Cardiac stem cells may become the most important cell for cardiac repair.
引用
收藏
页码:1373 / 1416
页数:44
相关论文
共 559 条
[1]   Stromal cell-derived factor-1α plays a critical role in stem cell recruitment to the heart after myocardial infarction but is not sufficient to induce homing in the absence of injury [J].
Abbott, JD ;
Huang, Y ;
Liu, D ;
Hickey, R ;
Krause, DS ;
Giordano, FJ .
CIRCULATION, 2004, 110 (21) :3300-3305
[2]   Maintenance of differentiation potential of human bone marrow mesenchymal stem cells immortalized by human telomerase reverse transcriptase gene in despite of extensive proliferation [J].
Abdallah, BM ;
Haack-Sorensen, M ;
Burns, JS ;
Elsnab, B ;
Jakob, F ;
Hokland, P ;
Kassem, M .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2005, 326 (03) :527-538
[3]   MRL mice fail to heal the heart in response to ischemia-reperfusion injury [J].
Abdullah, I ;
Lepore, JJ ;
Epstein, JA ;
Parmacek, MS ;
Gruber, PJ .
WOUND REPAIR AND REGENERATION, 2005, 13 (02) :205-208
[4]   Tissue injury in marrow transdifferentiation [J].
Abedi, M ;
Greer, DA ;
Colvin, GA ;
Demers, DA ;
Dooner, MS ;
Harpel, JA ;
Pimentel, J ;
Menon, MK ;
Quesenberry, PJ .
BLOOD CELLS MOLECULES AND DISEASES, 2004, 32 (01) :42-46
[5]   CELLS, MATRIX, GROWTH-FACTORS, AND THE SURGEON - THE BIOLOGY OF SCARLESS FETAL WOUND REPAIR [J].
ADZICK, NS ;
LORENZ, HP .
ANNALS OF SURGERY, 1994, 220 (01) :10-18
[6]   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
[7]   Gene recombination in postmitotic cells - Targeted expression of cre recombinase provokes cardiac-restricted, site-specific rearrangement in adult ventricular muscle in vivo [J].
Agah, R ;
Frenkel, PA ;
French, BA ;
Michael, LH ;
Overbeek, PA ;
Schneider, MD .
JOURNAL OF CLINICAL INVESTIGATION, 1997, 100 (01) :169-179
[8]   Mesenchymal stem cells: Isolation and therapeutics [J].
Alhadlaq, A ;
Mao, JJ .
STEM CELLS AND DEVELOPMENT, 2004, 13 (04) :436-448
[9]   Recipes for adult stem cell plasticity: fusion cuisine or readymade? [J].
Alison, MR ;
Poulsom, R ;
Otto, WR ;
Vig, P ;
Brittan, M ;
Direkze, NC ;
Lovell, M ;
Fang, TC ;
Preston, SL ;
Wright, NA .
JOURNAL OF CLINICAL PATHOLOGY, 2004, 57 (02) :113-120
[10]   Plastic adult stem cells: will they graduate from the school of hard knocks? [J].
Alison, MR ;
Poulsom, A ;
Otto, WR ;
Vig, P ;
Brittan, M ;
Direkze, NC ;
Preston, SL ;
Wright, NA .
JOURNAL OF CELL SCIENCE, 2003, 116 (04) :599-603