The role of endothelial progenitor and cardiac stem cells in the cardiovascular adaptations to age and exercise

被引：31
作者：
Thijssen, Dick H. J. [3 ]
Torella, Daniele [1 ,2 ]
Hopman, Maria T. E.
Ellison, Georgina M. [1 ]
机构：
[1] Liverpool John Moores Univ, Res Inst Sport & Exercise Sci, Stem Cell & Mol Physiol Lab, Liverpool L3 3ET, Merseyside, England
[2] Magna Graecia Univ Catanzaro, Lab Mol & Cellular Cardiol, I-88100 Catanzaro, Italy
[3] Radboud Univ Nijmegen, Med Ctr, Inst Fundamental & Clin Movement Sci, Dept Physiol, NL-6500 HB Nijmegen, Netherlands
来源：
FRONTIERS IN BIOSCIENCE-LANDMARK | 2009年 / 14卷
关键词：
Aging; Endothelial Progenitor Cells; Cardiac Stem Cells; Cardiovascular Disease; Exercise; Review; BONE-MARROW-CELLS; CORONARY-ARTERY-DISEASE; NITRIC-OXIDE SYNTHASE; SIDE POPULATION CELLS; GROWTH-FACTOR; HEMATOPOIETIC STEM; MYOCARDIAL-INFARCTION; DEPENDENT IMPAIRMENT; SMOOTH-MUSCLE; NEOVASCULARIZATION CAPACITY;
D O I：
10.2741/3560
中图分类号：
Q5 [生物化学]; Q7 [分子生物学];
学科分类号：
071010 ; 081704 ;
摘要：
Age is a major risk factor for cardiovascular disease. Many hypotheses have been proposed to explain the ageing process. Ageing of tissue-specific as well as circulating stem and progenitor cell compartments can be viewed to be central to the decline of tissue and organ integrity and function in the elderly. Related to the cardiovascular system, circulating endothelial progenitor cells (EPCs) contribute to the endothelial integrity and function, and initiate adult neovascularization, while resident cardiac stem cells (CSCs) have the potential to differentiate into cardiomyocytes, endothelial or smooth muscle cells in the heart. Reduction in number and functional capacity of EPCs and CSCs might play a role in age-related vascular and cardiac dysfunction, leading to increased cardiovascular risk. In this review, we discuss the impact of ageing on EPCs and CSCs and their possible contribution to age-related cardiovascular adaptations. Regular aerobic physical activity has a strong cardioprotective effect, while physical inactivity is a central part of the aging process. Therefore, we also outline the immediate and long-term effects of physical activity on EPCs and CSCs.
引用
收藏
页码：4685 / 4702
页数：18
相关论文
共 148 条
[1]   Increase of circulating endothelial progenitor cells in patients with coronary artery disease after exercise-induced ischemia [J].
Adams, V ;
Lenk, K ;
Linke, A ;
Lenz, D ;
Erbs, S ;
Sandri, M ;
Tarnok, A ;
Gielen, S ;
Emmrich, F ;
Schuler, G ;
Hambrecht, R .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2004, 24 (04) :684-690
[2]   Essential role of endothelial nitric oxide synthase for mobilization of stem and progenitor cells [J].
Aicher, A ;
Heeschen, C ;
Mildner-Rihm, C ;
Urbich, C ;
Ihling, C ;
Technau-Ihling, K ;
Zeiher, AM ;
Dimmeler, S .
NATURE MEDICINE, 2003, 9 (11) :1370-1376
[3]   Isolation of putative progenitor endothelial cells for angiogenesis [J].
Asahara, T ;
Murohara, T ;
Sullivan, A ;
Silver, M ;
vanderZee, R ;
Li, T ;
Witzenbichler, B ;
Schatteman, G ;
Isner, JM .
SCIENCE, 1997, 275 (5302) :964-967
[4]   Bone marrow origin of endothelial progenitor cells responsible for postnatal vasculogenesis in physiological and pathological neovascularization [J].
Asahara, T ;
Masuda, H ;
Takahashi, T ;
Kalka, C ;
Pastore, C ;
Silver, M ;
Kearne, M ;
Magner, M ;
Isner, JM .
CIRCULATION RESEARCH, 1999, 85 (03) :221-228
[5]   VEGF contributes to postnatal neovascularization by mobilizing bone marrow-derived endothelial progenitor cells [J].
Asahara, T ;
Takahashi, T ;
Masuda, H ;
Kalka, C ;
Chen, DH ;
Iwaguro, H ;
Inai, Y ;
Silver, M ;
Isner, JM .
EMBO JOURNAL, 1999, 18 (14) :3964-3972
[6]   Transplantation of progenitor cells and regeneration enhancement in acute myocardial infarction -: (TOPCARE-AMI) [J].
Assmus, B ;
Schächinger, V ;
Teupe, C ;
Britten, M ;
Lehmann, R ;
Döbert, N ;
Grünwald, F ;
Aicher, A ;
Urbich, C ;
Martin, H ;
Hoelzer, D ;
Dimmeler, S ;
Zeiher, AM .
CIRCULATION, 2002, 106 (24) :3009-3017
[7]   Stem cell factor receptor induces progenitor and natural killer cell-mediated cardiac survival and repair after myocardial infarction [J].
Ayach, BB ;
Yoshimitsu, M ;
Dawood, F ;
Sun, M ;
Arab, S ;
Chen, M ;
Higuchi, K ;
Siatskas, C ;
Lee, P ;
Lim, H ;
Zhang, J ;
Cukerman, E ;
Stanford, WL ;
Medin, JA ;
Liu, PP .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2006, 103 (07) :2304-2309
[8]   Haematopoietic stem cells adopt mature haematopoietic fates in ischaemic myocardium [J].
Balsam, LB ;
Wagers, AJ ;
Christensen, JL ;
Kofidis, T ;
Weissman, IL ;
Robbins, RC .
NATURE, 2004, 428 (6983) :668-673
[9]   Cardiopoietic programming of embryonic stem cells for tumor-free heart repair [J].
Behfar, Atta ;
Perez-Terzic, Carmen ;
Faustino, Randolph S. ;
Arrell, D. Kent ;
Hodgson, Denice M. ;
Yamada, Satsuki ;
Puceat, Michel ;
Niederlander, Nicolas ;
Alekseev, Alexey E. ;
Zingman, Leonid V. ;
Terzic, Andre .
JOURNAL OF EXPERIMENTAL MEDICINE, 2007, 204 (02) :405-420
[10]   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
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