Mitochondria form contact sites with the nucleus to couple prosurvival retrograde response.
Radha DesaiDaniel A EastLiana HardyDanilo FaccendaManuel RigonJames CrosbyMaría Soledad AlvarezAarti SinghMarta MainentiLaura Kuhlman HusseyRobert BenthamGyorgy SzabadkaiValentina ZappulliGurtej K DhootLisa E RomanoDong XiaIsabelle CoppensAnne Hamacher-BradyJ Paul ChappleRosella AbetiRoland A FleckGema Vizcay-BarrenaKenneth SmithMichelangelo CampanellaPublished in: Science advances (2020)
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.
Keyphrases
- nuclear factor
- toll like receptor
- cell death
- transcription factor
- protein kinase
- reactive oxygen species
- signaling pathway
- oxidative stress
- binding protein
- endoplasmic reticulum
- lps induced
- pet imaging
- low density lipoprotein
- inflammatory response
- computed tomography
- protein protein
- amino acid
- stress induced
- positron emission tomography