Inhibition of TRPP3 by calmodulin through Ca2+/calmodulin-dependent protein kinase II

Xiong Liu , Yifang Wang , Ziyi Weng , Qinyi Xu , Cefan Zhou , JingFeng Tang , Xing-Zhen Chen
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Abstract

Transient receptor potential (TRP) polycystin-3 (TRPP3) is a non-selective cation channel activated by Ca2+ and protons and is involved in regulating ciliary Ca2+ concentration, hedgehog signaling and sour tasting. The TRPP3 channel function and regulation are still not well understood. Here we investigated regulation of TRPP3 by calmodulin (CaM) by means of electrophysiology and Xenopus oocytes as an expression model. We found that TRPP3 channel function is enhanced by calmidazolium, a CaM antagonist, and inhibited by CaM through binding of the CaM N-lobe to a TRPP3 C-terminal domain not overlapped with the EF-hand. We further revealed that the TRPP3/CaM interaction promotes phosphorylation of TRPP3 at threonine 591 by Ca2+/CaM-dependent protein kinase II, which mediates the inhibition of TRPP3 by CaM.

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钙调素通过Ca2+/钙调素依赖性蛋白激酶II抑制TRPP3
瞬时受体电位(TRP)多囊蛋白-3(TRPP3)是一种由Ca2+和质子激活的非选择性阳离子通道,参与调节纤毛Ca2+浓度、刺猬信号传导和酸味。TRPP3通道的功能和调节仍不清楚。本文以非洲爪蟾卵母细胞为表达模型,通过电生理学研究了钙调蛋白(CaM)对TRPP3的调控。我们发现TRPP3通道功能被CaM拮抗剂calmidazolium增强,并通过CaM N叶与TRPP3 C末端结构域的结合被CaM抑制,该结构域与EF手不重叠。我们进一步揭示了TRPP3/CaM相互作用通过Ca2+/CaM依赖性蛋白激酶II促进TRPP3在苏氨酸591的磷酸化,其介导CaM对TRPP3的抑制。
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来源期刊
Cell insight
Cell insight Neuroscience (General), Biochemistry, Genetics and Molecular Biology (General), Cancer Research, Cell Biology
CiteScore
2.70
自引率
0.00%
发文量
0
审稿时长
35 days
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