Endothelial progenitor cells: identity defined?

被引:384
作者
Timmermans, Frank [1 ,2 ]
Plum, Jean [1 ]
Yoeder, Mervin C. [3 ,4 ,5 ]
Ingram, David A. [3 ,4 ,5 ]
Vandekerckhove, Bart [1 ]
Case, Jamie [3 ,4 ]
机构
[1] Univ Ghent, State Univ Ghent Hosp, Dept Clin Chem Microbiol & Immunol, B-9000 Ghent, Belgium
[2] Univ Ghent, State Univ Ghent Hosp, Dept Cardiovasc Med, B-9000 Ghent, Belgium
[3] Indiana Univ, Sch Med, Dept Pediat, Indianapolis, IN 46202 USA
[4] Indiana Univ, Sch Med, Herman B Wells Ctr Pediat Res, Indianapolis, IN 46202 USA
[5] Indiana Univ, Sch Med, Dept Biochem & Mol Biol, Indianapolis, IN 46202 USA
基金
美国国家卫生研究院;
关键词
endothelial progenitor cells; haematopoietic cells; CD34; CD45; CD133; MARROW-DERIVED CELLS; HEMATOPOIETIC STEM-CELLS; ACUTE MYOCARDIAL-INFARCTION; HUMAN PERIPHERAL-BLOOD; BONE-MARROW; IN-VIVO; VASCULAR ENDOTHELIUM; CD34(+) CELLS; TUMOR ANGIOGENESIS; MONONUCLEAR-CELLS;
D O I
10.1111/j.1582-4934.2008.00598.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
In the past decade, researchers have gained important insights on the role of bone marrow (BM)-derived cells in adult neovascularization. A subset of BM-derived cells, called endothelial progenitor cells (EPCs), has been of particular interest, as these cells were suggested to home to sites of neovascularization and neoendothelialization and differentiate into endothelial cells (ECs) in situ, a process referred to as postnatal vasculogenesis. Therefore, EPCs were proposed as a potential regenerative tool for treating human vascular disease and a possible target to restrict vessel growth in tumour pathology. However, conflicting results have been reported in the field, and the identification, characterization, and exact role of EPCs in vascular biology is still a subject of much discussion. The focus of this review is on the controversial issues in the field of EPCs which are related to the lack of a unique EPC marker, identification challenges related to the paucity of EPCs in the circulation, and the important phenotypical and functional overlap between EPCs, haematopoietic cells and mature ECs. We also discuss our recent findings on the origin of endothelial outgrowth cells (EOCs), showing that this in vitro defined EC population does not originate from circulating CD133(+) cells or CD45(+) haematopoietic cells.
引用
收藏
页码:87 / 102
页数:16
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