PI(4,5) P2-Dependent and Ca2+-Regulated ER-PM Interactions Mediated by the Extended Synaptotagmins

被引:463
作者
Giordano, Francesca [1 ,3 ,4 ]
Saheki, Yasunori [1 ,3 ,4 ]
Idevall-Hagren, Olof [1 ,3 ,4 ]
Colombo, Sara Francesca [5 ,6 ]
Pirruccello, Michelle [1 ,3 ,4 ]
Milosevic, Ira [1 ,3 ,4 ]
Gracheva, Elena O. [2 ,3 ]
Bagriantsev, Sviatoslav N. [2 ]
Borgese, Nica [5 ,6 ,7 ]
De Camilli, Pietro [1 ,3 ,4 ]
机构
[1] Yale Univ, Sch Med, Dept Cell Biol, New Haven, CT 06510 USA
[2] Yale Univ, Sch Med, Dept Physiol, New Haven, CT 06510 USA
[3] Yale Univ, Sch Med, Program Cellular Neurosci Neurodegenerat & Repair, New Haven, CT 06510 USA
[4] Yale Univ, Sch Med, Howard Hughes Med Inst, New Haven, CT 06510 USA
[5] Univ Milan, CNR, Inst Neurosci, I-20129 Milan, Italy
[6] Univ Milan, BIOMETRA Dept, I-20129 Milan, Italy
[7] Magna Graecia Univ Catanzaro, Dept Hlth Sci, I-88100 Catanzaro, Italy
基金
瑞典研究理事会;
关键词
ENDOPLASMIC-RETICULUM; PHOSPHOLIPID-BINDING; MEMBRANE-PROTEINS; CONTACT SITES; CA2+ SENSOR; STORE; DOMAINS; COMPLEX; STIM1; FORM;
D O I
10.1016/j.cell.2013.05.026
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Most available information on endoplasmic reticulum (ER)-plasma membrane (PM) contacts in cells of higher eukaryotes concerns proteins implicated in the regulation of Ca2+ entry. However, growing evidence suggests that such contacts play more general roles in cell physiology, pointing to the existence of additionally ubiquitously expressed ER-PM tethers. Here, we show that the three extended synaptotagmins (E-Syts) are ER proteins that participate in such tethering function via C2 domain-dependent interactions with the PM that require PI(4,5) P-2 in the case of E-Syt2 and E-Syt3 and also elevation of cytosolic Ca2+ in the case of E-Syt1. As they form heteromeric complexes, the E-Syts confer cytosolic Ca2+ regulation to ER-PM contact formation. E-Syts-dependent contacts, however, are not required for store-operated Ca2+ entry. Thus, the ER-PM tethering function of the E-Syts (tricalbins in yeast) mediates the formation of ER-PM contacts sites, which are functionally distinct from those mediated by STIM1 and Orai1.
引用
收藏
页码:1494 / 1509
页数:16
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