| Literature DB >> 24558039 |
Levente Jozsef1, Keitaro Tashiro, Andrew Kuo, Eon Joo Park, Athanasia Skoura, Sebastian Albinsson, Felix Rivera-Molina, Kenneth D Harrison, Yasuko Iwakiri, Derek Toomre, William C Sessa.
Abstract
Despite recent advances in understanding store-operated calcium entry (SOCE) regulation, the fundamental question of how ER morphology affects this process remains unanswered. Here we show that the loss of RTN4, is sufficient to alter ER morphology and severely compromise SOCE. Mechanistically, we show this to be the result of defective STIM1-Orai1 coupling because of loss of ER tubulation and redistribution of STIM1 to ER sheets. As a functional consequence, RTN4-depleted cells fail to sustain elevated cytoplasmic Ca(2+) levels via SOCE and therefor are less susceptible to Ca(2+) overload induced apoptosis. Thus, for the first time, our results show a direct correlation between ER morphology and SOCE and highlight the importance of RTN4 in cellular Ca(2+) homeostasis.Entities:
Keywords: Apoptosis; Cell Signaling; Endoplasmic Reticulum (ER); Imaging; Membrane; reticulons
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Year: 2014 PMID: 24558039 PMCID: PMC3969502 DOI: 10.1074/jbc.M114.548602
Source DB: PubMed Journal: J Biol Chem ISSN: 0021-9258 Impact factor: 5.157