Biology of bone marrow-derived endothelial cell precursors

被引:123
作者
Schatteman, Gina C.
Dunnwald, Martine
Jiao, Chunhua
机构
[1] Univ Iowa, Dept Integrat Physiol, Iowa City, IA 52242 USA
[2] Univ Iowa, Dept Dermatol, Iowa City, IA 52242 USA
来源
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY | 2007年 / 292卷 / 01期
关键词
endothelial progenitor cell; endothelium; tumorigenesis; stromal derived factor 1; monocyte;
D O I
10.1152/ajpheart.00662.2006
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Over the past decade, the old idea that the bone marrow contains endothelial cell precursors has become an area of renewed interest. While some still believe that there are no endothelial precursors in the blood, even among those who do, there is no consensus as to what they are or what they do. In this review, we describe the problems in identifying endothelial cells and conclude that expression of endothelial nitric oxide synthase may be the most reliable antigenic indicator of the phenotype. The evidence for two different classes of endothelial precursors is also presented. We suggest that, though there is no single endothelial cell precursor, we may be able to use these phenotypic variations to our advantage in better understanding their biology. We also discuss how a variety of genetic, epigenetic, and methodological differences can account for the seemingly contradictory findings on the physiological relevance of bone marrow-derived precursors in normal vascular maintenance and in response to injury. Data on the impact of tumor type and location on the contribution of bone marrow-derived cells to the tumor vasculature are also presented. These data provide hope that we may ultimately be able to predict those tumors in which bone marrow-derived cells will have a significant contribution and design therapies accordingly. Finally, factors that regulate bone marrow cell recruitment to and function in the endothelium are beginning to be identified, and several of these, including stromal derived factor 1, monocyte chemoattractant factor-1, and vascular endothelial growth factor are discussed.
引用
收藏
页码:H1 / H18
页数:18
相关论文
共 209 条
[21]   Skin graft vascularization involves precisely regulated regression and replacement of endothelial cells through both angiogenesis and vasculogenesis [J].
Capla, JM ;
Ceradini, D ;
Tepper, OM ;
Callaghan, MJ ;
Bhatt, KA ;
Galiano, RD ;
Levine, JP ;
Gurtner, GC .
PLASTIC AND RECONSTRUCTIVE SURGERY, 2006, 117 (03) :836-844
[22]   Mechanisms of angiogenesis and arteriogenesis [J].
Carmeliet, P .
NATURE MEDICINE, 2000, 6 (04) :389-395
[23]   Synergism between vascular endothelial growth factor and placental growth factor contributes to angiogenesis and plasma extravasation in pathological conditions [J].
Carmeliet, P ;
Moons, L ;
Luttun, A ;
Vincenti, V ;
Compernolle, V ;
De Mol, M ;
Wu, Y ;
Bon, F ;
Devy, L ;
Beck, H ;
Scholz, D ;
Acker, T ;
DiPalma, T ;
Dewerchin, M ;
Noel, A ;
Stalmans, I ;
Barra, A ;
Blacher, S ;
Vandendriessche, T ;
Ponten, A ;
Eriksson, U ;
Plate, KH ;
Foidart, JM ;
Schaper, W ;
Charnock-Jones, DS ;
Hicklin, DJ ;
Herbert, JM ;
Collen, D ;
Persico, MG .
NATURE MEDICINE, 2001, 7 (05) :575-583
[24]   Progenitor cell trafficking is regulated by hypoxic gradients through HIF-1 induction of SDF-1 [J].
Ceradini, DJ ;
Kulkarni, AR ;
Callaghan, MJ ;
Tepper, OM ;
Bastidas, N ;
Kleinman, ME ;
Capla, JM ;
Galiano, RD ;
Levine, JP ;
Gurtner, GC .
NATURE MEDICINE, 2004, 10 (08) :858-864
[25]   Hematopoietic stem cell quiescence maintained by p21cip1/waf1 [J].
Cheng, T ;
Rodrigues, N ;
Shen, HM ;
Yang, YG ;
Dombkowski, D ;
Sykes, M ;
Scadden, DT .
SCIENCE, 2000, 287 (5459) :1804-1808
[26]  
CIVIN CI, 1984, J IMMUNOL, V133, P157
[27]   Adult human hematopoietic cells provide functional hemangioblast activity [J].
Cogle, CR ;
Wainman, DA ;
Jorgensen, ML ;
Guthrie, SM ;
Mames, RN ;
Scott, EW .
BLOOD, 2004, 103 (01) :133-135
[28]  
Consigny PM, 2000, J LONG-TERM EFF MED, V10, P79
[29]   LABEL-RETAINING CELLS RESIDE IN THE BULGE AREA OF PILOSEBACEOUS UNIT - IMPLICATIONS FOR FOLLICULAR STEM-CELLS, HAIR CYCLE, AND SKIN CARCINOGENESIS [J].
COTSARELIS, G ;
SUN, TT ;
LAVKER, RM .
CELL, 1990, 61 (07) :1329-1337
[30]   EXISTENCE OF SLOW-CYCLING LIMBAL EPITHELIAL BASAL CELLS THAT CAN BE PREFERENTIALLY STIMULATED TO PROLIFERATE - IMPLICATIONS ON EPITHELIAL STEM-CELLS [J].
COTSARELIS, G ;
CHENG, SZ ;
DONG, G ;
SUN, TT ;
LAVKER, RM .
CELL, 1989, 57 (02) :201-209