| |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Vascular Biology |
From the Departments of Pharmacology (Y.I., M.S., H. Iwao) and Cardiology and Internal Medicine (M.Y., T.O., J.Y.), Osaka City University Medical School, Japan; the Departments of Pharmacology and Molecular Therapeutics (S.K.-M.) and Cell Pathology (M.T.), Kumamoto University Graduate School of Medical Sciences, Japan; Faculty of Education and Social Welfare (T.Y.), Ohtani Womens University, Tondabayashi, Japan; the Department of Cardiology (T.M.), Nagoya University Graduate School of Medicine, Japan; and the Laboratory of Cell Signaling, Graduate School of Pharmaceutical Sciences (A.M., H. Ichijo), University of Tokyo, Japan.
Correspondence to Shokei Kim-Mitsuyama, MD, Department of Pharmacology and Molecular Therapeutics, Kumamoto University Graduate School of Medical Sciences, 1-1-1 Honjo, Kumamoto 860-8556, Japan. E-mail kimmitsu{at}gpo.kumamoto-u.ac.jp
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 peroxideinduced 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.
We examined the significance of apoptosis signal-regulating kinase 1 (ASK1) in ischemia-induced angiogenesis in vivo. Well-developed collateral vessels and angiogenesis were observed in wild-type mice in response to hindlimb ischemia, whereas these responses were reduced in mice deficient in ASK1. Thus, the activation of ASK1 leads to angiogenesis.
Key Words: angiogenesis ischemia inflammation signal transduction cytokines
This article has been cited by other articles:
![]() |
E. Yamamoto, K. Kataoka, H. Shintaku, T. Yamashita, Y. Tokutomi, Y.-F. Dong, S. Matsuba, H. Ichijo, H. Ogawa, and S. Kim-Mitsuyama Novel Mechanism and Role of Angiotensin II Induced Vascular Endothelial Injury in Hypertensive Diastolic Heart Failure Arterioscler. Thromb. Vasc. Biol., December 1, 2007; 27(12): 2569 - 2575. [Abstract] [Full Text] [PDF] |
||||
![]() |
T. Yamashita, E. Yamamoto, K. Kataoka, T. Nakamura, S. Matsuba, Y. Tokutomi, Y.-F. Dong, H. Ichijo, H. Ogawa, and S. Kim-Mitsuyama Apoptosis Signal-Regulating Kinase-1 Is Involved in Vascular Endothelial and Cardiac Remodeling Caused by Nitric Oxide Deficiency Hypertension, September 1, 2007; 50(3): 519 - 524. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. C. Frisbee, J. B. Samora, J. Peterson, and R. Bryner Exercise training blunts microvascular rarefaction in the metabolic syndrome Am J Physiol Heart Circ Physiol, November 1, 2006; 291(5): H2483 - H2492. [Abstract] [Full Text] [PDF] |
||||
|
ATVB Home | Subscriptions | Archives | Feedback | Authors | Help | AHA Journals Home | Search Copyright © 2005 American Heart Association, Inc. All rights reserved. Unauthorized use prohibited. |