2015 Fiscal Year Final Research Report
Stabilizing endocrine cell function by phogrin.
Project/Area Number |
24390050
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Research Category |
Grant-in-Aid for Scientific Research (B)
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Allocation Type | Partial Multi-year Fund |
Section | 一般 |
Research Field |
General physiology
|
Research Institution | Gunma University |
Principal Investigator |
TORII SEIJI 群馬大学, 生体調節研究所, 准教授 (40312904)
|
Co-Investigator(Renkei-kenkyūsha) |
GOMI Hiroshi 日本大学, 生物資源科学部, 教授 (90293240)
NAMEKI Nobukazu 群馬大学, 工学研究科, 准教授 (80302959)
MOGAMI Hideo 浜松大学, 健康科学部, 教授 (90311604)
|
Project Period (FY) |
2012-04-01 – 2016-03-31
|
Keywords | ペプチドホルモン / 分泌顆粒 / インスリン / オートクライン / チロシンホスファターゼ |
Outline of Final Research Achievements |
Phogrin, a member of receptor protein tyrosine phosphatases, primarily localizes on secretory granules (SGs) in a variety of neuroendocrine cells including pancreatic β-cells, and has some supportive roles in SGs formation and cell growth. We analyze its function with use of newly developed imaging method and of gene-targeting mice. Our data show an evidence suggesting that at the plasma membrane phogrin participates in molecular interactions with insulin receptors to regulate IRS2 protein stability and in turn glucose-promoted pancreatic β-cell growth. We further showed that phogrin supports PTP1B activity to achieve an overall regulation of glucose-stimulated insulin signaling.
|
Free Research Field |
神経内分泌細胞学
|