Endothelial progenitor cells: past, state of the art, and future

被引:77
作者
Iwami, Y
Masuda, H
Asahara, T [1 ]
机构
[1] Tokai Univ, Sch Med, Dept Regenerat Med Sci, Isehara, Kanagawa 2591193, Japan
[2] Kobe Inst Biomed Res, Stem Cell Translat Res & Innovat, Kobe, Hyogo, Japan
[3] RIKEN, Ctr Dev Biol, Chuo Ku, Kobe, Hyogo, Japan
关键词
endothelial progenitor cell (EPC); vasculogenesis; angiogenesis; therapeutic neovascularization; cardiovascular disease; cell therapy;
D O I
10.1111/j.1582-4934.2004.tb00473.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Recent evidences suggest that endothelial progenitor cells (EPCs) derived from bone marrow (BM) contribute to de novo vessel formation in adults occurring as physiological and pathological responses. Emerging preclinical trials have shown that EPCs home to sites of neovascularization after ischemic events in limb and myocardium. On the basis of these aspects, EPCs are expected to develop as a key strategy of therapeutic applications for the ischemic organs. Such clinical requirements of EPCs will tentatively accelerate the translational research aiming at the devices to acquire the optimized quality and quantity of EPCs. In this review, we attempt to discuss about biological features of EPCs and speculate on the clinical potential of EPCs for therapeutic neovascularization.
引用
收藏
页码:488 / 497
页数:10
相关论文
共 41 条
[1]   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
[2]   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
[3]   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
[4]   Enhanced endothelialization and microvessel formation in polyester grafts seeded with CD34+ bone marrow cells [J].
Bhattacharya, V ;
McSweeney, PA ;
Shi, Q ;
Bruno, B ;
Ishida, A ;
Nash, R ;
Storb, RF ;
Sauvage, LR ;
Hammond, WP ;
Wu, MHD .
BLOOD, 2000, 95 (02) :581-585
[5]   Endothelial cells of hematopoietic origin make a significant contribution to adult blood vessel formation [J].
Crosby, JR ;
Kaminski, WE ;
Schatteman, G ;
Martin, PJ ;
Raines, EW ;
Seifert, RA ;
Bowen-Pope, DF .
CIRCULATION RESEARCH, 2000, 87 (09) :728-730
[6]   HMG-CoA reductase inhibitors (statins) increase endothelial progenitor cells via the PI 3-kinase/Akt pathway [J].
Dimmeler, S ;
Aicher, A ;
Vasa, M ;
Mildner-Rihm, C ;
Adler, K ;
Tiemann, M ;
Rütten, H ;
Fichtlscherer, S ;
Martin, H ;
Zeiher, AM .
JOURNAL OF CLINICAL INVESTIGATION, 2001, 108 (03) :391-397
[7]   Young adult bone marrow-derived endothelial precursor cells restore aging-impaired cardiac angiogenic function [J].
Edelberg, JM ;
Tang, LL ;
Hattori, K ;
Lyden, D ;
Rafii, S .
CIRCULATION RESEARCH, 2002, 90 (10) :E89-E93
[8]  
Gehling UM, 2000, BLOOD, V95, P3106
[9]  
Gill M, 2001, CIRC RES, V88, P167
[10]  
Gunsilius E, 2001, LANCET, V357, P1449, DOI 10.1016/S0140-6736(00)04605-5