| Literature DB >> 33355129 |
Radha Desai1, Daniel A East1, Liana Hardy1, Danilo Faccenda1, Manuel Rigon1, James Crosby1, María Soledad Alvarez1, Aarti Singh1, Marta Mainenti1, Laura Kuhlman Hussey1, Robert Bentham2, Gyorgy Szabadkai2,3,4, Valentina Zappulli5, Gurtej K Dhoot1, Lisa E Romano6, Dong Xia1, Isabelle Coppens7, Anne Hamacher-Brady7, J Paul Chapple6, Rosella Abeti8, Roland A Fleck9, Gema Vizcay-Barrena9, Kenneth Smith10, Michelangelo Campanella11,2.
Abstract
Mitochondria drive cellular adaptation to stress by retro-communicating with the nucleus. This process is known as mitochondrial retrograde response (MRR) and is induced by mitochondrial dysfunction. MRR results in the nuclear stabilization of prosurvival transcription factors such as the nuclear factor kappa-light-chain-enhancer of activated B cells (NF-κB). Here, we demonstrate that MRR is facilitated by contact sites between mitochondria and the nucleus. The translocator protein (TSPO) by preventing the mitophagy-mediated segregation o mitochonria is required for this interaction. The complex formed by TSPO with the protein kinase A (PKA), via the A-kinase anchoring protein acyl-CoA binding domain containing 3 (ACBD3), established the tethering. The latter allows for cholesterol redistribution of cholesterol in the nucleus to sustain the prosurvival response by blocking NF-κB deacetylation. This work proposes a previously unidentified paradigm in MRR: the formation of contact sites between mitochondria and nucleus to aid communication.Entities:
Year: 2020 PMID: 33355129 DOI: 10.1126/sciadv.abc9955
Source DB: PubMed Journal: Sci Adv ISSN: 2375-2548 Impact factor: 14.136