Analysis of process from ER stress to cell death in an animal model for disease
Project/Area Number |
23659475
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Research Category |
Grant-in-Aid for Challenging Exploratory Research
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Allocation Type | Multi-year Fund |
Research Field |
Endocrinology
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Research Institution | Nagoya University |
Principal Investigator |
OISO Yutaka 名古屋大学, 医学(系)研究科(研究院), 教授 (40203707)
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Co-Investigator(Kenkyū-buntansha) |
ARIMA Hiroshi 名古屋大学, 大学院医学系研究科, 准教授 (50422770)
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Project Period (FY) |
2011 – 2013
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Project Status |
Completed (Fiscal Year 2013)
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Budget Amount *help |
¥3,510,000 (Direct Cost: ¥2,700,000、Indirect Cost: ¥810,000)
Fiscal Year 2013: ¥1,170,000 (Direct Cost: ¥900,000、Indirect Cost: ¥270,000)
Fiscal Year 2012: ¥1,170,000 (Direct Cost: ¥900,000、Indirect Cost: ¥270,000)
Fiscal Year 2011: ¥1,170,000 (Direct Cost: ¥900,000、Indirect Cost: ¥270,000)
|
Keywords | バゾプレシン / 小胞体ストレス / オートファギー / 細胞死 |
Research Abstract |
Familial neurohypophysial diabetes insipidus (FNDI) model mice were subjected to intermittent water deprivation in order to promote the phenotypes. Electron microscopic analyses demonstrated that, while aggregates are confined to a certain compartment of the ER in the AVP neurons of FNDI mice with water access ad libitum, they were scattered throughout the dilated ER lumen in the FNDI mice subjected to water deprivation for 4 weeks. It is also demonstrated that phagophores, the autophagosome precursors, emerged in the vicinity of aggregates and engulfed the ER containing scattered aggregates. The cytoplasm of AVP neurons in FNDI mice was occupied with vacuoles in the mice subjected to water deprivation for 12 weeks, when 30-40% of AVP neurons are lost. Our data thus demonstrated that autophagy was induced in the AVP neurons subjected to ER stress in FNDI mice.
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Report
(4 results)
Research Products
(15 results)
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[Journal Article] Arginine vasopressin neuronal loss results from autophagy-associated cell death in a mouse model for familial neurohypophysial diabetes insipidus2014
Author(s)
Hagiwara D, Arima H, Morishita Y, Wenjun L, Azuma Y, Ito Y, Suga H, Goto M, Banno R, Sugimura Y, Shiota A, Asai N, Takahashi M, Oiso Y
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Journal Title
Cell Death Dis
Volume: 27;5
Related Report
Peer Reviewed
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