Mechanisms and roles of spatio-temporal dynamics of SAPKs signaling in determining cell fates.
Project/Area Number |
23770141
|
Research Category |
Grant-in-Aid for Young Scientists (B)
|
Allocation Type | Multi-year Fund |
Research Field |
Functional biochemistry
|
Research Institution | The University of Tokyo |
Principal Investigator |
|
Project Period (FY) |
2011 – 2012
|
Project Status |
Completed (Fiscal Year 2012)
|
Budget Amount *help |
¥4,550,000 (Direct Cost: ¥3,500,000、Indirect Cost: ¥1,050,000)
Fiscal Year 2012: ¥2,210,000 (Direct Cost: ¥1,700,000、Indirect Cost: ¥510,000)
Fiscal Year 2011: ¥2,340,000 (Direct Cost: ¥1,800,000、Indirect Cost: ¥540,000)
|
Keywords | ストレス応答 / キナーゼ / イメージング / 細胞死 / ストレス応答シグナル |
Research Abstract |
(1)Subcellular distribution of stress-activated protein kinase activities were determined by imaging analysis using fluorescent protein-based kinase activity sensors. (2) I found SAPKs are activated either in the cytoplasm or near plasma membrane depending on the type of stresses applied. (3)By manipulating subcellular-localized SAPK activity using inducible protein dimerization system, I found that cell death was induced only when sustained SAPK activity was induced in cytoplasm, while induction of transient SAPK activity resulted in no obvious cell death and showed only slight change in plasma membrane dynamics (membrane brebbing and shape of cell edge). Our data suggest that SAPK mediated signal can determine cell fates depending on the spatial or temporal dynamics of SAPK activity inside cells.
|
Report
(3 results)
Research Products
(9 results)