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Important role of apoptosis signal-regulating kinase 1 in ischemia-induced angiogenesis

delete2005-09-01
delete34
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OA
AI
Y
Yasukatsu Izumi
S
Shokei Kim‐Mitsuyama
M
Minoru Yoshiyama
T
Takashi Omura
M
Masayuki Shiota
A
Atsushi Matsuzawa
T
Tokihito Yukimura
T
Toyoaki Murohara
M
Motohiro Takeya
H
Hidenori Ichijo
J
Junichi Yoshikawa
H
Hiroshi Iwao
DOI:10.1161/01.ATV.0000174801.76234.bddelete
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Abstract

Abstract

En 中文
Objective - We first examined the role of apoptosis signal-regulating kinase 1 (ASK1), one of mitogen-activated protein kinase kinase kinases, in ischemia-induced angiogenesis. Methods and Results - Unilateral hindlimb ischemia was induced surgically in C57BL/6J wild-type (WT) mice or mice deficient in ASK1 ( ASK1(-/-)). ASK1 activity in WT mouse hindlimb was increased dramatically after ischemia. By laser Doppler analysis, well-developed collateral vessels and angiogenesis were observed in WT mice in response to hindlimb ischemia, whereas these responses were reduced in ASK1(-/-) mice. Immunostaining revealed that infiltration of macrophages and T lymphocytes was suppressed in the ischemic tissues of ASK1(-/-) mice compared with WT mice. The expression of vascular endothelial growth factor ( VEGF) and monocyte chemoattractant protein-1 (MCP-1) proteins in ischemic tissues was weaker in ASK1(-/-) mice compared with WT mice. In vitro study on endothelial cells indicated that dominant-negative ASK1 significantly attenuated hydrogen peroxide - induced VEGF and MCP-1 production. Furthermore, in vivo blockade of MCP-1 by its neutralizing antibody suppressed the recovery of the blood flow and capillary formation after ischemia. Conclusions - ASK1 pathway promotes early angiogenesis by inducing inflammatory cell infiltration and VEGF and MCP-1 expression. ASK1 may provide the basis for the development of new therapeutic strategy for angiogenesis.
Keywords:
angiogenesis
ischemia
inflammation
signal transduction
cytokines
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Journal

Arteriosclerosis Thrombosis and Vascular Biology cover
Arteriosclerosis Thrombosis and Vascular Biology
IF:
7.4
Papers:
1.2W
Citations:
3.5W

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