Endothelial progenitor cells as factors in neovascularization and endothelial repair

被引:24
作者
Capobianco, Stefano [1 ]
Chennamaneni, Venu [2 ]
Mittal, Mayank [2 ]
Zhang, Nannan [3 ]
Zhang, Cuihua [3 ]
机构
[1] Gaetano Rummo Hosp, Dept Cardiol, Via DellAngelo 1, Benevento 82100, Italy
[2] Univ Missouri, Dept Internal Med, Columbia, MO 65211 USA
[3] Univ Missouri, Dalton Cardiovascular Res Ctr, Dept Internal Medi cine Med Pharmacol & Physiol, Columbia, MO 65211 USA
来源
WORLD JOURNAL OF CARDIOLOGY | 2010年 / 2卷 / 12期
关键词
Atherosclerosis; Bone marrow; Endothelial dysfunction; Endothelial progenitor cells; Neovascularization; Stem cells;
D O I
10.4330/wjc.v2.i12.411
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Endothelial progenitor cells (EPCs) are a heterogeneous population of cells that are provided by the bone marrow and other adult tissue in both animals and humans. They express both hematopoietic and endothelial surface markers, which challenge the classic dogma that the presumed differentiation of cells into angioblasts and subsequent endothelial and vascular differentiation occurred exclusively in embryonic development. This breakthrough stimulated research to understand the mechanism(s) underlying their physiologic function to allow development of new therapeutic options. One focus has been on their ability to form new vessels in injured tissues, and another has been on their ability to repair endothelial damage and restore both monolayer integrity and endothelial function in denuded vessels. Moreover, measures of their density have been shown to be a better predictor of cardiovascular events, both in healthy and coronary artery disease populations than the classical tools used in the clinic to evaluate the risk stratification. In the present paper we review the effects of EPCs on revascularization and endothelial repair in animal models and human studies, in an attempt to better understand their function, which may lead to potential advancement in clinical management. (C 2010 Baishideng. All rights reserved.
引用
收藏
页码:411 / 420
页数:10
相关论文
共 105 条
[1]   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
[2]   Long-term follow-up of patients with mild coronary artery disease and endothelial dysfunction [J].
Al Suwaidi, J ;
Hamasaki, S ;
Higano, ST ;
Nishimura, RA ;
Holmes, DR ;
Lerman, A .
CIRCULATION, 2000, 101 (09) :948-954
[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]   Effect of stromal-cell-derived factor 1 on stem-cell homing and tissue regeneration in ischaemic cardiomyopathy [J].
Askari, AT ;
Unzek, S ;
Popovic, ZB ;
Goldman, CK ;
Forudi, F ;
Kiedrowski, M ;
Rovner, A ;
Ellis, SG ;
Thomas, JD ;
DiCorleto, PE ;
Topol, EJ ;
Penn, MS .
LANCET, 2003, 362 (9385) :697-703
[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]   Effects of cerivastatin on human arterial smooth muscle cell proliferation and migration in transfilter cocultures [J].
Axel, DI ;
Riessen, R ;
Runge, H ;
Viebahn, R ;
Karsch, KR .
JOURNAL OF CARDIOVASCULAR PHARMACOLOGY, 2000, 35 (04) :619-629
[8]   Protein kinase B (c-Akt), phosphatidylinositol 3-kinase, and STAT5 are activated by erythropoietin (EPO) in HCD57 erythroid cells but are constitutively active in an EPO-independent, apoptosis-resistant subclone (HCD57-SREI cells) [J].
Bao, HF ;
Jacobs-Helber, SM ;
Lawson, AE ;
Penta, K ;
Wickrema, A ;
Sawyer, ST .
BLOOD, 1999, 93 (11) :3757-3773
[9]   High levels of circulating endothelial microparticles in patients with acute coronary syndromes [J].
Bernal-Mizrachi, L ;
Jy, W ;
Jimenez, JJ ;
Pastor, J ;
Mauro, LM ;
Horstman, LL ;
de Marchena, E ;
Ahn, YS .
AMERICAN HEART JOURNAL, 2003, 145 (06) :962-970
[10]   VASCULAR-PERMEABILITY FACTOR (VASCULAR ENDOTHELIAL GROWTH-FACTOR) GENE IS EXPRESSED DIFFERENTIALLY IN NORMAL-TISSUES, MACROPHAGES, AND TUMORS [J].
BERSE, B ;
BROWN, LF ;
VANDEWATER, L ;
DVORAK, HF ;
SENGER, DR .
MOLECULAR BIOLOGY OF THE CELL, 1992, 3 (02) :211-220