| Literature DB >> 26903221 |
Jessica Matesanz-Isabel1, Jessica Arias-del-Val1, Pilar Alvarez-Illera1, Rosalba I Fonteriz1, Mayte Montero1, Javier Alvarez2.
Abstract
MICU1 and MICU2 are the main regulators of the mitochondrial Ca(2+)-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 [Ca(2+)] ([Ca(2+)]c), though its effects decrease as [Ca(2+)]c is increased and disappear above 7 μM. 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 Ca(2+) 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 [Ca(2+)]c, separate and kinetically different from that of MICU2. On the other hand, we and others have shown previously that MICU1 activates MCU at [Ca(2+)]c above 2.5 μM. Thus, MICU1 has a double role in MCU regulation, inhibitory at low [Ca(2+)]c and activatory at high [Ca(2+)]c.Entities:
Keywords: Aequorin; Calcium; HeLa cells; MCU; MICU1; MICU2
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Year: 2016 PMID: 26903221 DOI: 10.1016/j.bbamem.2016.02.022
Source DB: PubMed Journal: Biochim Biophys Acta ISSN: 0006-3002