2013
DOI: 10.1016/j.cmet.2013.04.020
|View full text |Cite
|
Sign up to set email alerts
|

MICU1 Controls Both the Threshold and Cooperative Activation of the Mitochondrial Ca2+ Uniporter

Abstract: Summary Mitochondrial Ca2+ uptake via the uniporter is central to cell metabolism, signaling and survival. Recent studies identified MCU as the uniporter’s likely pore and MICU1, an EF-hand protein, as its critical regulator. How this complex decodes dynamic cytoplasmic [Ca2+] ([Ca2+]c) signals, to tune out small [Ca2+]c increases yet permit pulse transmission, remains unknown. We report that loss of MICU1 in mouse liver and cultured cells causes mitochondrial Ca2+ accumulation during small [Ca2+]c elevations,… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1
1
1

Citation Types

59
490
1
6

Year Published

2014
2014
2023
2023

Publication Types

Select...
6
2

Relationship

2
6

Authors

Journals

citations
Cited by 411 publications
(556 citation statements)
references
References 49 publications
59
490
1
6
Order By: Relevance
“…However, as the defect in mitochondrial Ca 2+ accumulation in Pat#1 cells is also evident in permeabilized cells (Supplementary Figure S3c), we conclude that the assembly of the MCU complex has a major role in lowering mitochondrial Ca 2+ uptake. In particular, Pat#1 and Pat#2 (but not Pat#3 and Pat#4) cells show a significant decrease of MICU1 and EMRE levels, known as positive MCU regulators, [15][16][17][18] and an increase in the expression of MICU2. MICU2 is a negative MCU modulator as it forms the MICU1/ MICU2 heterodimer, thus sequestering MICU1 and preventing the MICU1 homodimer stimulatory activity on MCU, as we recently demonstrated.…”
Section: Discussionmentioning
confidence: 95%
See 1 more Smart Citation
“…However, as the defect in mitochondrial Ca 2+ accumulation in Pat#1 cells is also evident in permeabilized cells (Supplementary Figure S3c), we conclude that the assembly of the MCU complex has a major role in lowering mitochondrial Ca 2+ uptake. In particular, Pat#1 and Pat#2 (but not Pat#3 and Pat#4) cells show a significant decrease of MICU1 and EMRE levels, known as positive MCU regulators, [15][16][17][18] and an increase in the expression of MICU2. MICU2 is a negative MCU modulator as it forms the MICU1/ MICU2 heterodimer, thus sequestering MICU1 and preventing the MICU1 homodimer stimulatory activity on MCU, as we recently demonstrated.…”
Section: Discussionmentioning
confidence: 95%
“…The pore region is composed of MCU, its isoform MCUb 14 and essential MCU regulator (EMRE). 15 The channel is gated by the Ca 2+ -sensitive proteins mitochondrial Ca 2+ uptake 1 (MICU1) and MICU2 [16][17][18][19] and further regulated by the SLC25A23 protein. 20 As to its cellular function, mitochondrial Ca 2+ has been shown to stimulate ATP production by positive regulation of three key dehydrogenases of the tricarboxylic acid cycle 21 and of the ETC.…”
mentioning
confidence: 99%
“…Control of mitochondrial Ca 2+ uptake can occur through a change in its driving force or the permeability of MCU. The latter is regulated for example by the Ca 2+ sensing MICU1 protein that supports closure of the MCU at low and cooperative activation of the MCU at high [Ca 2+ ] c [53][54][55].…”
Section: Role Of Pic In Calcium Handlingmentioning
confidence: 99%
“…Therefore, the precise role of the PiC in mitochondrial Ca 2+ uptake requires further investigation. Since Pi likely is a primary factor in mitochondrial matrix Ca 2+ buffering that shows remarkable adaptive changes during both acute and prolonged increases in mitochondrial Ca 2+ uptake [53,59], the mechanisms of the coordination of the transports of Pi and Ca 2+ is of great interest. Although mitochondrial ATP production is an obvious major target of PiC deficiency, downstream effects of a limitation in mitochondrial ATP production may have their own consequences.…”
Section: Future Directionsmentioning
confidence: 99%
“…[Ca 2ϩ ] o was measured using fura2 (1.5 M) for [Ca 2ϩ ] o range 0 to ϳ2.5 M or fura-loAff (1 M) for [Ca 2ϩ ] o Ͼ2.5 M. Fura fluorescence was recorded and transformed to molar [Ca 2ϩ ] values as described (36). Despite the Ca 2ϩ -free isolation procedure at 0 -4°C, significant Ca 2ϩ residue remained in the SR store of the SR fraction.…”
Section: Camentioning
confidence: 99%