The CCT chaperonin is a novel regulator of Ca2+ signaling through modulation of Orai1 trafficking

Rawad Hodeify, Manjula Nandakumar, Maryam Own, Raphael Jean Courjaret, Johannes Graumann, Satanay Zuhair Hubrack, Khaled Machaca

Research output: Contribution to journalArticle

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Abstract

Store-operated Ca2+ entry (SOCE) encodes a range of cellular responses downstream of Ca2+ influx through the SOCE channel Orai1. Orai1 recycles at the plasma membrane (PM), with ∼40% of the total Orai1 pool residing at the PM at steady state. The mechanisms regulating Orai1 recycling remain poorly understood. We map the domains in Orai1 that are required for its trafficking to and recycling at the PM. We further identify, using biochemical and proteomic approaches, the CCT [chaperonin-containing TCP-1 (T-complex protein 1)] chaperonin complex as a novel regulator of Orai1 recycling by primarily regulating Orai1 endocytosis. We show that Orai1 interacts with CCT through its intracellular loop and that inhibition of CCT-Orai1 interaction increases Orai1 PM residence. This increased residence is functionally significant as it results in prolonged Ca2+ signaling, early formation of STIM1-Orai1 puncta, and more rapid activation of NFAT (nuclear factor of activated T cells) downstream of SOCE. Therefore, the CCT chaperonin is a novel regulator of Orai1 trafficking and, as such, a modulator of Ca2+ signaling and effector activation kinetics.

Original languageEnglish
Article numberaau1935
JournalScience advances
Volume4
Issue number9
DOIs
Publication statusPublished - 26 Sep 2018

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Chaperonin Containing TCP-1
Recycling
Cell Membrane
Chaperonins
NFATC Transcription Factors
Endocytosis
Proteomics

ASJC Scopus subject areas

  • General

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The CCT chaperonin is a novel regulator of Ca2+ signaling through modulation of Orai1 trafficking. / Hodeify, Rawad; Nandakumar, Manjula; Own, Maryam; Courjaret, Raphael Jean; Graumann, Johannes; Hubrack, Satanay Zuhair; Machaca, Khaled.

In: Science advances, Vol. 4, No. 9, aau1935, 26.09.2018.

Research output: Contribution to journalArticle

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