Pericyte Regulation of Vascular Remodeling Through the CXC Receptor 3

被引:55
作者
Bodnar, Richard J. [1 ,3 ]
Rodgers, Margaret E.
Chen, William C. W. [2 ]
Wells, Alan [1 ,3 ]
机构
[1] Univ Pittsburgh, Dept Pathol, Pittsburgh, PA 15260 USA
[2] Univ Pittsburgh, Dept Bioengn, Pittsburgh, PA 15260 USA
[3] Pittsburgh Vet Affairs Med Ctr, Pittsburgh, PA USA
基金
美国国家卫生研究院;
关键词
angiogenesis; CXC chemokine receptor 3; endothelial cells; pericytes; wound healing; ENDOTHELIAL GROWTH-FACTOR; CHEMOKINE RECEPTOR-3; TUBE FORMATION; CELL GROWTH; TNF-ALPHA; PDGF-B; INHIBITION; ANGIOGENESIS; REGRESSION; IP-10;
D O I
10.1161/ATVBAHA.113.302012
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective To understand the role, if any, played by pericytes in the regulation of newly formed vessels during angiogenesis. In this study, we investigate whether pericytes regulate the number of nascent endothelial tubes. Approach and Results Using an in vitro angiogenesis assay (Matrigel assay), we demonstrate that pericytes can inhibit vessel formation and induce vessel dissociation via CXCR3-induced involution of the endothelial cells. In a coculture Matrigel assay for cord formation, pericytes prevented endothelial cord formation of human dermal microvascular endothelial cells but not umbilical vein endothelial cells. Blockade of endothelial CXCR3 function or expression inhibited the repressing effect of the pericytes. We further show that pericytes are also able to induce regression of newly formed microvascular cords through CXCR3 activation of calpain. When CXCR3 function was inhibited by a neutralizing antibody or downregulated by siRNA, cord regression mediated by pericytes was abolished. Conclusions We show for the first time that pericytes regulate angiogenic vessel formation, and that this is mediated through CXCR3 expressed on endothelial cells. This suggests a role for pericytes in the pruning of immature vessels overproduced during wound repair.
引用
收藏
页码:2818 / 2829
页数:12
相关论文
共 51 条
[1]   HMEC-1 - ESTABLISHMENT OF AN IMMORTALIZED HUMAN MICROVASCULAR ENDOTHELIAL-CELL LINE [J].
ADES, EW ;
CANDAL, FJ ;
SWERLICK, RA ;
GEORGE, VG ;
SUMMERS, S ;
BOSSE, DC ;
LAWLEY, TJ .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1992, 99 (06) :683-690
[2]   Pericytes: Cell biology and pathology [J].
Allt, G ;
Lawrenson, JG .
CELLS TISSUES ORGANS, 2001, 169 (01) :1-11
[3]   Angiogenesis in the bovine corpus luteum:: An immunocytochemical and ultrastructural study [J].
Amselgruber, WM ;
Schäfer, M ;
Sinowatz, F .
ANATOMIA HISTOLOGIA EMBRYOLOGIA-JOURNAL OF VETERINARY MEDICINE SERIES C-ZENTRALBLATT FUR VETERINARMEDIZIN REIHE C, 1999, 28 (03) :157-166
[4]   Endothelial/pericyte interactions [J].
Armulik, A ;
Abramsson, A ;
Betsholtz, C .
CIRCULATION RESEARCH, 2005, 97 (06) :512-523
[5]  
Babu M, 2001, WOUNDS, V13, P183
[6]   Regulated angiogenesis and vascular regression in mice overexpressing vascular endothelial growth factor in airways [J].
Baluk, P ;
Lee, CG ;
Link, H ;
Ator, E ;
Haskell, A ;
Elias, JA ;
McDonald, DM .
AMERICAN JOURNAL OF PATHOLOGY, 2004, 165 (04) :1071-1085
[7]   Growth factors and cytokines in wound healing [J].
Barrientos, Stephan ;
Stojadinovic, Olivera ;
Golinko, Michael S. ;
Brem, Harold ;
Tomic-Canic, Marjana .
WOUND REPAIR AND REGENERATION, 2008, 16 (05) :585-601
[8]  
Benjamin LE, 1998, DEVELOPMENT, V125, P1591
[9]  
Betsholtz C, 2005, EXP SUPPL, V94, P115
[10]   IP-10 induces dissociation of newly formed blood vessels [J].
Bodnar, Richard J. ;
Yates, Cecelia C. ;
Rodgers, Margaret E. ;
Du, Xiaoping ;
Wells, Alan .
JOURNAL OF CELL SCIENCE, 2009, 122 (12) :2064-2077