2016 Fiscal Year Final Research Report
Investigation of the role of Menin in immunosenescense and cellular energy metabolism
Project/Area Number |
15K19133
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Research Category |
Grant-in-Aid for Young Scientists (B)
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Allocation Type | Multi-year Fund |
Research Field |
Immunology
|
Research Institution | Ehime University |
Principal Investigator |
Suzuki Junpei 愛媛大学, 医学系研究科, 助教(特定教員) (20734239)
|
Research Collaborator |
Yasukawa Masaki
Yamashita Masakatsu
|
Project Period (FY) |
2015-04-01 – 2017-03-31
|
Keywords | T細胞老化 / 細胞内エネルギー代謝 / mTORC1 |
Outline of Final Research Achievements |
The deficiency in Menin, a tumor suppressor protein, induces CD8 T-cell senescence. We found that Akt/mTORC1 signaling pathway was enhanced in Menin-deficient activated CD8 T cells. We performed a metabolic profiling of 116 metabolites and found that Menin-deficient activated CD8 T cells had higher rate of glutaminolysis and anaerobic glycolysis than that in the WT activated CD8 T cells. Furthermore, premature CD8 T cell senescence in Menin-deficient CD8 T cells was partially inhibited by the treatment with rapamycin or inhibitors for glutamine metabolism. Theses results suggest that Menin controls CD8 T-cell senescence in part by regulating the energy metabolism.
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Free Research Field |
免疫学
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