A modest change in housing temperature alters whole body energy expenditure and adipocyte thermogenic capacity in mice

• Published in: American journal of physiology: endocrinology and metabolism Vol. 323; no. 6; p. E517
• Main Authors: Sadler, Daniel G, Treas, Lillie, Sikes, James D, Porter, Craig
• Format: Journal Article
• Language: English
• Published: United States 01-12-2022
• Subjects: Adipose Tissue, Brown - metabolism; Adipose Tissue, White - metabolism; Animals; Energy Metabolism; Female; Humans; Male; Mice; Mice, Inbred C57BL; Proteomics; Thermogenesis; Uncoupling Protein 1 - metabolism; adipose tissue; thermoneutral; ambient temperature; thermogenesis; proteomics
• ISSN: 1522-1555
• DOI: 10.1152/ajpendo.00079.2022

Typical vivarium temperatures (20-26°C) induce facultative thermogenesis in mice, a process attributable in part to uncoupling protein-1 (UCP1). The impact of modest changes in housing temperature on whole body and adipose tissue energetics in mice remains unclear. Here, we determined the effects of transitioning mice from 24°C to 30°C on total energy expenditure and adipose tissue protein signatures. C57BL/6J mice were housed at 24°C for 2 wk and then either remained at 24°C (
= 16/group, 8M/8F) or were transitioned to 30°C (
= 16/group, 8M/8F) for 4 wk. Total energy expenditure and its components were determined by indirect calorimetry. Interscapular brown adipose tissue (iBAT) and inguinal white adipose tissue (iWAT) proteins were quantified by Western blot and quantitative proteomics. Transitioning from 24°C to 30°C reduced total energy expenditure in both male (-25%) and female (-16%) mice, which was attributable to lower basal energy expenditure in males (-36%) and females (-40%). Total iBAT UCP1 protein content was 50% lower at 30°C compared with 24°C, whereas iWAT UCP1 protein content was similar between conditions. iBAT UCP1 protein content remained 20-fold greater than iWAT at 30°C. In iBAT and iWAT, 183 and 41 proteins were differentially expressed between 24°C and 30°C, respectively. iWAT proteins (257) differentially expressed between sexes at 30°C were not differentially expressed at 24°C. Thus, 30°C housing lowers total energy expenditure of mice when compared with an ambient temperature (24°C) that falls within the National Research Council's guidelines for housing laboratory mice. Lower iBAT UCP1 content accompanied chronic housing at 30°C. Furthermore, housing temperature influences sexual dimorphism in the iWAT proteome. These data have implications regarding the optimization of preclinical models of human disease.
Housing mice at 30°C reduced the basal and total energy expenditure compared with 24°C, which was accompanied by a reduction in brown adipose tissue UCP1 content. Proteomic profiling demonstrated the brown adipose tissue and white adipose tissue proteomes were largely influenced by housing temperature and sex, respectively. Therefore, 30°C housing revealed sexual dimorphism in the white adipose tissue proteome that was largely absent in animals housed at 24°C.