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2019年3月6日

iCeMS見学グループセミナー:Mengping Wei 博士

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 このたび、高等研究院物質-細胞統合システム拠点 (iCeMS) 見学グループでは、
セミナーを以下の通り開催いたします。
事前申し込みは不要ですので、皆様のご参加をお待ちしております。

Mengping Wei 博士
State Key Laboratory of Membrane Biology, School of Life Sciences, Peking University

ABHD6 negatively regulates the trafficking and function of AMPA receptors
Regulation of AMPA receptor (AMPAR)-mediated synaptic transmission is a key mechanism for synaptic plasticity. High-resolution proteomics analysis revealed that native AMPARs were macromolecular complex including a number of auxiliary subunits, including TARPs, CNIHs, GSG1L and CKAMP44, which are important for AMPARs forward trafficking to synapses. Our studies shows that ABHD6 negatively regulates AMPAR-mediated synaptic transmission. Overexpression of ABHD6 in neurons drastically reduced, and ABHD6 knockout (KO) enhances, excitatory neurotransmission mediated by AMPARs and surface expression levels of AMPARs. Interestingly, overexpression of ABHD6 reduced glutamate-induced currents and the surface expression of GluA1 in HEK293T cells expressing GluA1 and stargazin, suggesting a direct functional interaction between ABHD6 and GluA1.The C-terminal tail of GluA1 was required for the binding between of ABHD6 and GluA1, suggested by pull down assay. Future analysis showed that overexpression of ABHD6 led to the retention of AMPARs in the endoplasmic reticulum and thus inhibited the surface delivery of AMPARs and AMPAR-mediated responses. Futuremore, overexpression of ABHD6 decreased the tau of desesitization. Finally, ABHD6 KO mice exhibited decreased LTP and incresed LTD. Thus, our findings reveal a novel and unexpected mechanism governing AMPAR trafficking at synapses through ABHD6.

日時
2019年3月8日(金)15:00〜16:00
場所
京都大学iCeMS本館2階 セミナールーム
事前登録
必要なし
言語
英語
主催・問い合わせ
京都大学 高等研究院 物質-細胞統合システム拠点(iCeMS)見学美根子グループ
kengaku-g [at] icems.kyoto-u.ac.jp

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