| Literature DB >> 28262504 |
Zhiwei Dong1, Santhanam Shanmughapriya2, Dhanendra Tomar2, Naveed Siddiqui3, Solomon Lynch4, Neeharika Nemani2, Sarah L Breves2, Xueqian Zhang5, Aparna Tripathi2, Palaniappan Palaniappan2, Massimo F Riitano2, Alison M Worth2, Ajay Seelam2, Edmund Carvalho2, Ramasamy Subbiah2, Fabián Jaña2, Jonathan Soboloff6, Yizhi Peng7, Joseph Y Cheung5, Suresh K Joseph8, Jeffrey Caplan4, Sudarsan Rajan9, Peter B Stathopulos3, Muniswamy Madesh10.
Abstract
Ca2+ dynamics and oxidative signaling are fundamental mechanisms for mitochondrial bioenergetics and cell function. The MCU complex is the major pathway by which these signals are integrated in mitochondria. Whether and how these coactive elements interact with MCU have not been established. As an approach toward understanding the regulation of MCU channel by oxidative milieu, we adapted inflammatory and hypoxia models. We identified the conserved cysteine 97 (Cys-97) to be the only reactive thiol in human MCU that undergoes S-glutathionylation. Furthermore, biochemical, structural, and superresolution imaging analysis revealed that MCU oxidation promotes MCU higher order oligomer formation. Both oxidation and mutation of MCU Cys-97 exhibited persistent MCU channel activity with higher [Ca2+]m uptake rate, elevated mROS, and enhanced [Ca2+]m overload-induced cell death. In contrast, these effects were largely independent of MCU interaction with its regulators. These findings reveal a distinct functional role for Cys-97 in ROS sensing and regulation of MCU activity.Entities:
Keywords: EMRE; MCU; MCUR1; MICU1; MICU2; bioenergetics; calcium; gluathionylation; mitochondria; reactive oxygen species
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Year: 2017 PMID: 28262504 PMCID: PMC5357178 DOI: 10.1016/j.molcel.2017.01.032
Source DB: PubMed Journal: Mol Cell ISSN: 1097-2765 Impact factor: 17.970