| Project/Area Number |
25293042
|
|---|
| Research Category |
Grant-in-Aid for Scientific Research (B)
|
| Allocation Type | Partial Multi-year Fund |
|---|
| Section | 一般 |
|---|
| Research Field |
General anatomy (including histology/embryology)
|
|---|
| Research Institution | Tokyo Medical and Dental University |
|---|
Principal Investigator |
NAKATA TAKAO 東京医科歯科大学, 医歯(薬)学総合研究科, 教授 (50218004)
|
|---|
| Co-Investigator(Kenkyū-buntansha) |
INOUE AKIHIRO 東京医科歯科大学, 大学院医歯学総合研究科, 准教授 (80322080)
ISHII TOMOHORO 東京医科歯科大学, 大学院医歯学総合研究科, 助教 (60549947)
|
|---|
| Project Period (FY) |
2013-04-01 – 2016-03-31
|
| Project Status |
Completed (Fiscal Year 2015)
|
| Budget Amount *help |
¥17,940,000 (Direct Cost: ¥13,800,000、Indirect Cost: ¥4,140,000)
Fiscal Year 2015: ¥2,080,000 (Direct Cost: ¥1,600,000、Indirect Cost: ¥480,000)
Fiscal Year 2014: ¥2,080,000 (Direct Cost: ¥1,600,000、Indirect Cost: ¥480,000)
Fiscal Year 2013: ¥13,780,000 (Direct Cost: ¥10,600,000、Indirect Cost: ¥3,180,000)
|
|---|
| Keywords | シグナル伝達 / G蛋白 / 細胞骨格 / 細胞運動 / 光スイッチ / 解剖学 / 細胞組織 / 神経科学 |
|---|
| Outline of Final Research Achievements |
Actin cytoskeletons play an important role in cell structure, division,
motility, development and signaling. Overexpression of the mutant GTPases as well as their gene-knock out studies revealed that RAC1 and CDC42 might regulate these processes, but cells might accommodate to the newsituation, resulting in less phenotypes. We performed acute-activation of photoactivatable (PA)-GTPases and observed the early phenotypes using life-act mCherry marker for F-actin in typical polygonal-shaped COS7 cells before/after light stimulation. RAC1 mainly acted on sides and formed laterally long lamellipodia (LP), while CDC42 polymerized actin filaments mainly at some vertexes (tips) of the cell and the actin bundles protrude into LP at the tips. Accordingly, the bundles were parallel to cell margins.
|
