Project/Area Number |
15K07969
|
Research Category |
Grant-in-Aid for Scientific Research (C)
|
Allocation Type | Multi-year Fund |
Section | 一般 |
Research Field |
Pharmacology in pharmacy
|
Research Institution | Kitasato University |
Principal Investigator |
|
Co-Investigator(Kenkyū-buntansha) |
藤井 健志 同志社女子大学, 薬学部, 教授 (80255380)
間下 雅士 同志社女子大学, 薬学部, 助教 (30738886)
堀口 和秀 福井大学, 学術研究院医学系部門, 准教授 (20377451)
|
Co-Investigator(Renkei-kenkyūsha) |
MISAWA Hidemi 慶応大学, 薬学部, 教授 (80219617)
MORIWAKI Yasuhiro 慶応大学, 薬学部, 講師 (00392150)
|
Project Period (FY) |
2015-04-01 – 2018-03-31
|
Project Status |
Completed (Fiscal Year 2017)
|
Budget Amount *help |
¥4,810,000 (Direct Cost: ¥3,700,000、Indirect Cost: ¥1,110,000)
Fiscal Year 2017: ¥780,000 (Direct Cost: ¥600,000、Indirect Cost: ¥180,000)
Fiscal Year 2016: ¥1,560,000 (Direct Cost: ¥1,200,000、Indirect Cost: ¥360,000)
Fiscal Year 2015: ¥2,470,000 (Direct Cost: ¥1,900,000、Indirect Cost: ¥570,000)
|
Keywords | nAChR / アロステリック・リガンド / Treg / Th1 / Th2 / GTS-21 / alpha7 / DO11.10マウス / T細胞分化 / alpha7 nAChR / 抗原提示細胞 / 制御性T細胞 / エフェクターT細胞 / SLURP-1 / Th分化 / Th17 / α7 nAChR / アロステリック・リガンド / T細胞 / 分化 |
Outline of Final Research Achievements |
We studied roles of GTS-21, an alpha7 (a7) nAChR agonist, and recombinant human type SLURP-1 (rhSLURP-1), an endogenous allosteric a7 nAChR ligand, in regulation of T cell differentiation. The differentiation was activated by culturing spleen cells from DO11.10 mice with ovalbumin (OVA) or OVA peptide (OVA-P). The effects of GTS-21 and rhSLURP-1 on T cell differentiation into regulatory T cell (Tregs) and effector T cells (Th1 and Th2) were determined by FACS or ELISA. GTS-21 inhibited the differentiation into Tregs and effector T cells under OVA activation, but facilitated the differentiation under OVA-P activation. rhSLURP-1 did not show any effect under the present experimental conditions. These results suggest that a7 nAChR activation in antigen-presenting cells prevents antigen processing leading to suppression of the differentiation while a7 nAChR activation in T cell facilitates the differentiation. No effect with rhSLURP-1 may be due to species difference.
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