Mitochondria form contact sites with the nucleus to couple pro-survival retrograde response
Desai, R.; East, D. A.; Hardy, L.; Rigon, M.; Faccenda, D.; Alvarex, M. S.; Singh, A.; Mainenti, M.; Hussey, L. K.; Bentham, R.; Szabadkai, G.; Zappulli, V.; Dhoot, G.; Romano, L. E.; Dong, X.; Coppens, I.; Hamacher-Brady, A.; Chapple, P.; Fleck, R. A.; Vizcay-Barrena, G.; Abeti, R.; Smith, K.; Campanella, M.
Show 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 dysfunctions which perturb cell signalling. MRR results in the nuclear stabilization and activation of pro-survival transcription factors such as the nuclear factor kappa-light-chain-enhancer of activated B cells (NF-kB). Here we demonstrate that MRR is facilitated by the formation of contact sites between mitochondria and the nucleus which establish microdomains of communication between the two organelles. The 18kD Translocator Protein (TSPO), which de-ubiquitylates and stabilizes the mitochondrial network preventing its mitophagy-mediated segregation, is required for this interaction. The tethering TSPO enacts is mediated by the complex formed with the Protein Kinase A via the A-kinase anchoring protein Acyl-CoA Binding Domain Containing 3 (ACBD3) and allows the redistribution of cholesterol which sustains the pro-survival response by blocking NF-kB de-acetylation. This work proposes a new paradigm in the mitochondrial retro-communication by revealing the existence of contact sites between mitochondrial and the nucleus and a signalling role for cholesterol.
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