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CXCL16 is a novel angiogenic factor for human umbilical vein endothelial cells
被引:91
作者:
Zhuge, X
Murayama, T
Arai, H
Yamauchi, R
Tanaka, M
Shimaoka, T
Yonehara, S
Kume, N
Yokode, M
Kita, T
机构:
[1] Kyoto Univ, Grad Sch Med, Dept Geriatr Med, Sakyo Ku, Kyoto 6068507, Japan
[2] Kyoto Univ, Grad Sch Med, Dept Clin Innovat Med, Sakyo Ku, Kyoto 6068507, Japan
[3] Kyoto Univ, Grad Sch Med, Dept Cardiovasc Med, Sakyo Ku, Kyoto 6068507, Japan
[4] Kyoto Univ, Grad Sch Med, Inst Virus Res, Sakyo Ku, Kyoto 6068507, Japan
关键词:
CXCL16;
angiogencsis;
endothelial cell;
D O I:
10.1016/j.bbrc.2005.03.200
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
CXCL16 is a unique chemokine with characteristics as a receptor for phosphatidylserine and oxidized low density lipoproteins in macrophages, and is involved in the accumulation of cellular cholesterol during atherosclerotic lesion development. In this study, we report a new function of CXCL16 as a novel angiogenic factor in human umbilical vein endothelial cells (HUVEC). CXCL16 stimulated proliferation and chemotaxis of HUVEC in a dose-dependent manner, reaching a maximum at 1 nM. CXCL16 also significantly induced tube formation of HUVEC on Matrigel. Further, exposure of HUVEC to CXCL16 led to a time- and dose-dependent activation of mitogen-activated protein kinase (ERK1/2), which was completely inhibited by a mitogen-activated protein kinase kinase inhibitor, PD98059. Proliferation and tube formation in response to CXCL16 were also blocked by the pretreatment with PD98059, but not CXCL16-induced chemotaxis. Thus, our data indicate that CXCL16 may act as a novel angiogenic factor for HUVEC and that ERK is involved as an important signaling molecule to mediate its angiogenic effects. (c) 2005 Elsevier Inc. All rights reserved.
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页码:1295 / 1300
页数:6
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