Cell
Volume 151, Issue 3, 26 October 2012, Pages 630-644
Journal home page for Cell

Article
MICU1 Is an Essential Gatekeeper for MCU-Mediated Mitochondrial Ca2+ Uptake that Regulates Cell Survival

https://doi.org/10.1016/j.cell.2012.10.011Get rights and content
Under an Elsevier user license
open archive

Summary

Mitochondrial Ca2+ (Ca2+m) uptake is mediated by an inner membrane Ca2+ channel called the uniporter. Ca2+ uptake is driven by the considerable voltage present across the inner membrane (ΔΨm) generated by proton pumping by the respiratory chain. Mitochondrial matrix Ca2+ concentration is maintained five to six orders of magnitude lower than its equilibrium level, but the molecular mechanisms for how this is achieved are not clear. Here, we demonstrate that the mitochondrial protein MICU1 is required to preserve normal [Ca2+]m under basal conditions. In its absence, mitochondria become constitutively loaded with Ca2+, triggering excessive reactive oxygen species generation and sensitivity to apoptotic stress. MICU1 interacts with the uniporter pore-forming subunit MCU and sets a Ca2+ threshold for Ca2+m uptake without affecting the kinetic properties of MCU-mediated Ca2+ uptake. Thus, MICU1 is a gatekeeper of MCU-mediated Ca2+m uptake that is essential to prevent [Ca2+]m overload and associated stress.

Highlights

▸ MICU1 inhibits the mitochondrial Ca2+ channel MCU under resting conditions ▸ MICU1 sets a cytoplasmic Ca2+ concentration threshold for mitochondrial Ca2+ uptake ▸ Loss of MICU1 results in mitochondrial Ca2+ overload ▸ Mitochondrial Ca2+ overload causes excessive ROS production and cell stress

Cited by (0)

8

These authors contributed equally to this work