2012 Fiscal Year Final Research Report
Systematic analysis of angiogenesis system and development of novel immunomodulation in organ acceptance and regeneration
Project/Area Number |
21390366
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Research Category |
Grant-in-Aid for Scientific Research (B)
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Allocation Type | Single-year Grants |
Section | 一般 |
Research Field |
General surgery
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Research Institution | Nara Medical University |
Principal Investigator |
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Co-Investigator(Kenkyū-buntansha) |
SHO Masayuki 奈良県立医科大学, 医学部, 准教授 (50364063)
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Project Period (FY) |
2009 – 2012
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Keywords | 臓器移植 / 拒絶反応 / 血管新生 |
Research Abstract |
The aim of this study was to clarify unknown mechanisms relating to angiogenesis in graft acceptance and tissue regeneration. Moreover, we aimed to develop novel therapeutic strategy inducing durable immunoregulation and long-term acceptance in organ and cell transplantation. We found that TWEAK/Fn14 pathway plays a critical role in ischemia-reperfusion injury. Importantly, Fn14 blockade had a significant inhibitory effect on inhibition of injury. In inflammatory bowel disease model, we うい erythropoietin, which has a proangiogenic property, was found to not only prevent tissue injury, but also accelerate tissue repair. These revealed mechanisms may lead to develop novel therapeutic strategy for intractable disease conditions.
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Research Products
(10 results)
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[Journal Article] Direct targeting of fibroblast growth factor-inducible 14 protein protects against renal ischemia reperfusion injury2011
Author(s)
Hotta K, Sho M, Yamato I, Shimada K, Harada H, Akahori T, Nakamura S, Konishi N, Yagita H, Nonomura K, Nakajima Y
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Journal Title
Kidney Int
Volume: 79(2)
Pages: 179-88
Peer Reviewed
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[Journal Article] Therapeutic potential of the TWEAK/Fn14 pathway in intractable gastrointestinal cancer2011
Author(s)
Yoriki R, Akashi S, Sho M, Nomi T, Yamato I, Hotta K, Takayama T, Matsumoto S, Wakatsuki K, Migita K, Yagita H, Nakajima Y
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Journal Title
Exp Ther Med
Volume: 2(1)
Pages: 103-108
Peer Reviewed
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