Regulation of epidermal innate immunity by Smurf/Arkadia
Project/Area Number |
25293245
|
Research Category |
Grant-in-Aid for Scientific Research (B)
|
Allocation Type | Partial Multi-year Fund |
Section | 一般 |
Research Field |
Dermatology
|
Research Institution | Ehime University |
Principal Investigator |
Koji Sayama 愛媛大学, 医学(系)研究科(研究院), 教授 (80187286)
|
Co-Investigator(Kenkyū-buntansha) |
Toyama Mikiko 愛媛大学, 大学院医学系研究科, 准教授 (60263935)
Shiraishi Ken 愛媛大学, 医学部附属病院, 講師 (80710863)
白方 裕司 愛媛大学, 医学(系)研究科(研究院), 准教授 (50226320)
|
Project Period (FY) |
2013-04-01 – 2016-03-31
|
Project Status |
Completed (Fiscal Year 2015)
|
Budget Amount *help |
¥18,590,000 (Direct Cost: ¥14,300,000、Indirect Cost: ¥4,290,000)
Fiscal Year 2015: ¥4,160,000 (Direct Cost: ¥3,200,000、Indirect Cost: ¥960,000)
Fiscal Year 2014: ¥5,590,000 (Direct Cost: ¥4,300,000、Indirect Cost: ¥1,290,000)
Fiscal Year 2013: ¥8,840,000 (Direct Cost: ¥6,800,000、Indirect Cost: ¥2,040,000)
|
Keywords | Innate immunity / keratinocyte / epidermis / TGF-beta / Smad / 自然免疫 / 角化細胞 / smad / KOマウス / 表皮角化細胞 / インフラマソーム / アレルギー |
Outline of Final Research Achievements |
Function of Smurf and Arkadia was analyzed in keratinocytes. Stimulation with TGF-beta enhanced Smad2/3 phosphorylation and Smad7 expression. While TGF-beta stimulation enhaced Smurf1/2 expression, it did not enhance the expression of Arkadia. The phosphorylation of Smad2/3 and the expression of Smad7 were significantly enhanced by reducing Smurf by using shRNA. On the other hand, suppression of Arkadia by shRNA reduced the phosphorylation of Smad2/3 and the expression of Smad7. Furthermore, suppressive effect of TGF-beta on cell growth and migration was enhanced by knockdown of Smurf.
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Report
(4 results)
Research Products
(11 results)