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2016 Fiscal Year Final Research Report

Investigation of the role of Menin in immunosenescense and cellular energy metabolism

Research Project

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Project/Area Number 15K19133
Research Category

Grant-in-Aid for Young Scientists (B)

Allocation TypeMulti-year Fund
Research Field Immunology
Research InstitutionEhime 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
KeywordsT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.

Free Research Field

免疫学

URL: 

Published: 2018-03-22  

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