STAT5 is required for lipid breakdown and beta-adrenergic responsiveness of brown adipose tissue

Mol Metab. 2020 Oct:40:101026. doi: 10.1016/j.molmet.2020.101026. Epub 2020 May 28.


Objective: Increasing energy expenditure through activation of brown adipose tissue (BAT) thermogenesis is an attractive approach to counteract obesity. It is therefore essential to understand the molecular mechanisms that control BAT functions. Until now several members of the Janus kinase (JAK) - signal transducer and activator of transcription (STAT) pathway have been implicated as being relevant for BAT physiology. However, whether the STAT family member STAT5 is important for the thermogenic property of adipose tissues is unknown. Therefore, we have investigated the role of STAT5 in thermogenic fat in this paper.

Methods: We performed metabolic and molecular analyses using mice that harbor an adipocyte-specific deletion of Stat5a/b alleles.

Results: We found that STAT5 is necessary for acute cold-induced temperature maintenance and the induction of lipid mobilization in BAT following β3-adrenergic stimulation. Moreover, mitochondrial respiration of primary differentiated brown adipocytes lacking STAT5 was diminished. Increased sensitivity to cold stress upon STAT5 deficiency was associated with reduced expression of thermogenic markers including uncoupling protein 1 (UCP1), while decreased stimulated lipolysis was linked to decreased protein kinase A (PKA) activity. Additionally, brown remodeling of white adipose tissue was diminished following chronic β3-adrenergic stimulation, which was accompanied by a decrease in mitochondrial performance.

Conclusion: We conclude that STAT5 is essential for the functionality and the β-adrenergic responsiveness of thermogenic adipose tissue.

Keywords: JAK-STAT; Temperature maintenance; Thermogenesis; β-adrenergic signalling.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adipocytes / metabolism
  • Adipose Tissue, Brown / metabolism*
  • Adipose Tissue, White / metabolism
  • Animals
  • Cold-Shock Response / physiology
  • Energy Metabolism
  • Female
  • Lipid Metabolism / physiology
  • Lipids / physiology
  • Lipolysis
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Mitochondria / metabolism
  • Obesity / metabolism
  • Receptors, Adrenergic, beta / metabolism
  • Receptors, Adrenergic, beta / physiology
  • STAT5 Transcription Factor / metabolism*
  • STAT5 Transcription Factor / physiology
  • Thermogenesis / physiology*


  • Lipids
  • Receptors, Adrenergic, beta
  • STAT5 Transcription Factor
  • Stat5a protein, mouse