mTORC1-PGC1 axis regulates mitochondrial remodeling during reprogramming

FEBS J. 2020 Jan;287(1):108-121. doi: 10.1111/febs.15024. Epub 2019 Aug 18.

Abstract

Metabolic reprogramming, hallmarked by enhanced glycolysis and reduced mitochondrial activity, is a key event in the early phase of somatic cell reprogramming. Although extensive work has been conducted to identify the mechanisms of mitochondrial remodeling in reprogramming, many questions remain. In this regard, different laboratories have proposed a role in this process for either canonical (ATG5-dependent) autophagy-mediated mitochondrial degradation (mitophagy), noncanonical (ULK1-dependent, ATG5-independent) mitophagy, mitochondrial fission or reduced biogenesis due to mTORC1 suppression. Clarifying these discrepancies is important for providing a comprehensive picture of metabolic changes in reprogramming. Yet, the comparison among these studies is difficult because they use different reprogramming conditions and mitophagy detection/quantification methods. Here, we have systematically explored mitochondrial remodeling in reprogramming using different culture media and reprogramming factor cocktails, together with appropriate quantification methods and thorough statistical analysis. Our experiments show lack of evidence for mitophagy in mitochondrial remodeling in reprogramming, and further confirm that the suppression of the mTORC1-PGC1 pathway drives this process. Our work helps to clarify the complex interplay between metabolic changes and nutrient sensing pathways in reprogramming, which may also shed light on other contexts such as development, aging and cancer.

Keywords: PGC1; mTORC1; mitochondrial remodeling; mitophagy; reprogramming.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Differentiation
  • Cells, Cultured
  • Cellular Reprogramming*
  • Embryonic Stem Cells / metabolism
  • Embryonic Stem Cells / pathology*
  • Fibroblasts / metabolism
  • Fibroblasts / pathology*
  • Glycolysis
  • Mechanistic Target of Rapamycin Complex 1 / genetics
  • Mechanistic Target of Rapamycin Complex 1 / metabolism*
  • Mice
  • Mice, Inbred ICR
  • Mitochondria / metabolism
  • Mitochondria / pathology*
  • Mitochondrial Dynamics
  • Mitophagy*
  • Transcription Factors / genetics
  • Transcription Factors / metabolism*

Substances

  • Transcription Factors
  • peroxisome-proliferator-activated receptor-gamma coactivator-1
  • Mechanistic Target of Rapamycin Complex 1