Roles of FABP and its regulating factors on neurogenesis after ischemia
Project/Area Number |
21591834
|
Research Category |
Grant-in-Aid for Scientific Research (C)
|
Allocation Type | Single-year Grants |
Section | 一般 |
Research Field |
Cerebral neurosurgery
|
Research Institution | University of Yamanashi |
Principal Investigator |
SUGITA Masao 山梨大学, 大学院・医学工学総合研究部, 医学研究員 (70235886)
|
Co-Investigator(Kenkyū-buntansha) |
KINOUCHI Hiroyuki 山梨大学, 医学工学総合研究部, 教授 (30241623)
|
Project Period (FY) |
2009 – 2011
|
Project Status |
Completed (Fiscal Year 2011)
|
Budget Amount *help |
¥4,550,000 (Direct Cost: ¥3,500,000、Indirect Cost: ¥1,050,000)
Fiscal Year 2011: ¥1,040,000 (Direct Cost: ¥800,000、Indirect Cost: ¥240,000)
Fiscal Year 2010: ¥1,820,000 (Direct Cost: ¥1,400,000、Indirect Cost: ¥420,000)
Fiscal Year 2009: ¥1,690,000 (Direct Cost: ¥1,300,000、Indirect Cost: ¥390,000)
|
Keywords | 脳虚血 / 脂肪酸結合蛋白 / 神経新生 / 神経細胞保護 |
Research Abstract |
Elucidating the mechanisms of neurogenesis after ischemia is crucial for the development of regenerative therapy for stroke. Brain-type fatty acid binding protein(B-FABP) is supposed to regulate neurogenesis during development and to have a cytoprotective role ; however, the roles on neurogenesis and neuronal injury after ischemia have not been studied well. In this study, we used a mouse forebrain ischemia model, and examined expression change of B-FABP after ischemia. In addition, we evaluated the effects of B-FABP gene knockout on neurogenesis and neuronal injury after ischemia. The current study revealed that B-FABP is expressed in neuronal stem cells, and regulates proliferation of neuronal stem cells under physiological and ischemic conditions, though the role of B-FABP on ischemic neuronal injury is not evident.
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Report
(4 results)
Research Products
(1 results)