The physiological role of TASK channel in adrenaline secretion
Project/Area Number |
26460306
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Research Category |
Grant-in-Aid for Scientific Research (C)
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Allocation Type | Multi-year Fund |
Section | 一般 |
Research Field |
General physiology
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Research Institution | University of Occupational and Environmental Health, Japan |
Principal Investigator |
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Project Period (FY) |
2014-04-01 – 2017-03-31
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Project Status |
Completed (Fiscal Year 2016)
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Budget Amount *help |
¥4,940,000 (Direct Cost: ¥3,800,000、Indirect Cost: ¥1,140,000)
Fiscal Year 2016: ¥910,000 (Direct Cost: ¥700,000、Indirect Cost: ¥210,000)
Fiscal Year 2015: ¥1,820,000 (Direct Cost: ¥1,400,000、Indirect Cost: ¥420,000)
Fiscal Year 2014: ¥2,210,000 (Direct Cost: ¥1,700,000、Indirect Cost: ¥510,000)
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Keywords | TASKチャネル / エンドサイトーシス / Src / TASK1 channel / endocytosis |
Outline of Final Research Achievements |
I investigated the function and physiological role of TASK1 channels in endocrine cells. Pharmacological and molecular biological analyses showed that TASK1 channels are regulated by the clathrin-dependent endocytosis in NGF- and muscarine-stimulated adrenal medullary and PC12 cells. Additionally, it showed that the molecular mechanisms regulating channel endocytosis differ between NGF-induced endocytosis and muscarine-induced endocytosis. The AM cells prepared from TASK1 KO mice indicated the decrease of pH sensitivity and adrenaline secretion, suggesting TASK1 channels play an important role in a sensor of acidosis and adrenaline secretion in AM cells.
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Report
(4 results)
Research Products
(8 results)
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[Journal Article] Fluorescent visualisation of the hypothalamic oxytocin neurones activated by cholecystokinin-8 in rats expressing c-fos-enhanced green fluorescent protein and oxtocin-monomeric red fluorescent protein 1 fusion transgenes.2014
Author(s)
Katoh, A. Shoguchi, K. Matsuoka, H. Yoshimura, M. Ohkubo,JI. Matsuura, T. Maruyama, T. Ishikura, T. Aritomi, T. Fujihara, H. Hashimoto, H. Suzuki, H. Murphy, D. & Ueta, Y.
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Journal Title
Journal of Neuroendocrinology
Volume: 26(5)
Issue: 5
Pages: 341-347
DOI
Related Report
Peer Reviewed / Open Access
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