Transcriptional Landscaping Identifies a Beige Adipocyte Depot in the Newborn Mouse

Cells. 2021 Sep 9;10(9):2368. doi: 10.3390/cells10092368.

Abstract

The present study sought to identify gene networks that are hallmarks of the developing inguinal subcutaneous adipose tissue (iWAT) and the interscapular brown adipose tissue (BAT) in the mouse. RNA profiling revealed that the iWAT of postnatal (P) day 6 mice expressed thermogenic and lipid catabolism transcripts, along with the abundance of transcripts associated with the beige adipogenesis program. This was an unexpected finding, as thermogenic BAT was believed to be the only site of nonshivering thermogenesis in the young mouse. However, the transcriptional landscape of BAT in P6 mice suggests that it is still undergoing differentiation and maturation, and that the iWAT temporally adopts thermogenic and lipolytic potential. Moreover, P6 iWAT and adult (P56) BAT were similar in their expression of immune gene networks, but P6 iWAT was unique in the abundant expression of antimicrobial proteins and virus entry factors, including a possible receptor for SARS-CoV-2. In summary, postnatal iWAT development is associated with a metabolic shift from thermogenesis and lipolysis towards fat storage. However, transcripts of beige-inducing signal pathways including β-adrenergic receptors and interleukin-4 signaling were underrepresented in young iWAT, suggesting that the signals for thermogenic fat differentiation may be different in early postnatal life and in adulthood.

Keywords: adipogenesis; adipose tissue; brown fat; obesity; thermogenesis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adipocytes, Beige / metabolism*
  • Adipose Tissue, Brown / metabolism
  • Adipose Tissue, White / metabolism
  • Animals
  • Animals, Newborn
  • Biomarkers / metabolism
  • Cell Cycle / genetics
  • Gene Expression Regulation, Developmental
  • Gene Ontology
  • Gene Regulatory Networks
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Models, Biological
  • Muscle Development / genetics
  • Neuropeptides / metabolism
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Signal Transduction
  • Transcription, Genetic*

Substances

  • Biomarkers
  • Neuropeptides
  • RNA, Messenger