Mitochondrial RNA stimulates beige adipocyte development in young mice

Nat Metab. 2022 Dec;4(12):1684-1696. doi: 10.1038/s42255-022-00683-w. Epub 2022 Nov 28.

Abstract

Childhood obesity is a serious public health crisis and a critical factor that determines future obesity prevalence. Signals affecting adipocyte development in early postnatal life have a strong potential to trigger childhood obesity; however, these signals are still poorly understood. We show here that mitochondrial (mt)RNA efflux stimulates transcription of nuclear-encoded genes for mitobiogenesis and thermogenesis in adipocytes of young mice and human infants. While cytosolic mtRNA is a potential trigger of the interferon (IFN) response, young adipocytes lack such a response to cytosolic mtRNA due to the suppression of IFN regulatory factor (IRF)7 expression by vitamin D receptor signalling. Adult and obese adipocytes, however, strongly express IRF7 and mount an IFN response to cytosolic mtRNA. In turn, suppressing IRF7 expression in adult adipocytes restores mtRNA-induced mitobiogenesis and thermogenesis and eventually mitigates obesity. Retrograde mitochondrion-to-nucleus signalling by mtRNA is thus a mechanism to evoke thermogenic potential during early adipocyte development and to protect against obesity.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adipocytes / physiology
  • Adipocytes, Beige* / metabolism
  • Adult
  • Animals
  • Child
  • Humans
  • Mice
  • Pediatric Obesity*
  • RNA, Mitochondrial / metabolism
  • Signal Transduction

Substances

  • RNA, Mitochondrial

Associated data

  • figshare/10.6084/m9.figshare.21202400