Litcius/Paper detail

TSG101 negatively regulates mitochondrial biogenesis in axons

Tzu-Huai Lin, Dana M. Bis‐Brewer, Amy E. Sheehan, Louise Townsend, Daniel C. Maddison, Stephan Züchner, Gaynor A. Smith, Marc Freeman

2021Proceedings of the National Academy of Sciences26 citationsDOIOpen Access PDF

Abstract

exhibited an increase in mitochondrial number and decrease in mitochondrial size. TSG101 is best known as a component of the endosomal sorting complexes required for transport (ESCRT) complexes; however, loss of most other ESCRT components did not affect mitochondrial numbers or size, suggesting TSG101 regulates mitochondrial biology in a noncanonical, ESCRT-independent manner. The TSG101-mutant phenotype was not caused by lack of mitophagy, and we found that autophagy blockade was detrimental only to the mitochondria in the cell bodies, arguing mitophagy and autophagy are dispensable for the regulation of mitochondria number in axons. Interestingly, TSG101 mitochondrial phenotypes were instead caused by activation of PGC-1ɑ/Nrf2-dependent mitochondrial biogenesis, which was mTOR independent and TFEB dependent and required the mitochondrial fission-fusion machinery. Our work identifies a role for TSG101 in inhibiting mitochondrial biogenesis, which is essential for the maintenance of mitochondrial numbers and sizes, in the axonal compartment.

Topics & Concepts

TSG101MitophagyPINK1MitochondrionBiologyCell biologyBiogenesismitochondrial fusionParkinMitochondrial biogenesisProteostasisNeuroscienceMitochondrial DNAAutophagyGeneticsParkinson's diseaseGeneDiseaseMedicineMicrovesiclesmicroRNAApoptosisPathologyMitochondrial Function and PathologyAutophagy in Disease and TherapyEndoplasmic Reticulum Stress and Disease