Functional roles of MICU1 and MICU2 in mitochondrial Ca2+ uptake

被引:36
|
作者
Matesanz-Isabel, Jessica
Arias-del-Val, Jessica
Alvarez-Illera, Pilar
Fonteriz, Rosalba I.
Montero, Mayte
Alvarez, Javier [1 ]
机构
[1] Univ Valladolid, Fac Med, IBGM, Dept Bioquim & Biol Mol & Fisiol, Ramon & Cajal 7, E-47005 Valladolid, Spain
来源
关键词
MCU; MICU1; MICU2; Aequorin; HeLa cells; Calcium; CALCIUM UNIPORTER; ESSENTIAL COMPONENT; PROTEIN; ACTIVATION; DYNAMICS; MCU; AEQUORIN; RELEASE;
D O I
10.1016/j.bbamem.2016.02.022
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
MICU1 and MICU2 are the main regulators of the mitochondrial Ca2+-uniporter (MCU), but their precise functional role is still under debate. We show here that MICU2 behaves as a pure inhibitor of MCU at low cytosolic [Ca2+] ([Ca2+](c)), though its effects decrease as [Ca2+], is increased and disappear above 7 mu M. Regarding MICU1, studying its effects is more difficult because knockdown of MICU1 leads also to loss of MICU2. However, while knockdown of MICU2 induces only a persistent increase in mitochondrial Ca2+ uptake, knockdown of MICU1 also induces a peculiar use-dependent transient activation of MCU that cannot be attributed to the parallel loss of MICU2. Therefore, MICU1 is endowed with a specific inhibitory effect on MCU at low [Ca2+](c), separate and kinetically different from that of MICU2. On the other hand, we and others have shown previously that MICU1 activates MCU at [Ca2+](c) above 2.5 mu M. Thus, MICU1 has a double role in MCU regulation, inhibitory at low [Ca2+](c) and activatory at high [Ca2+](c). (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:1110 / 1117
页数:8
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