Journal
CELLULAR AND MOLECULAR LIFE SCIENCES
Volume 79, Issue 8, Pages -Publisher
SPRINGER BASEL AG
DOI: 10.1007/s00018-022-04441-9
Keywords
Adtrp; BAT; iWAT; Thermogenesis; Differentiation; S100b
Categories
Funding
- National Natural Science Foundation of China [82171854, 31970802]
- Beijing Municipal Natural Science Foundation [7202099]
- Medical University of Bialystok, Poland [SUB/1/DN/20/006/1104]
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Brown and beige adipose tissues play a crucial role in maintaining body temperature and their impaired function can lead to metabolic diseases. This study identified a functional thermogenic regulator, Adtrp, which was significantly overexpressed in mature brown/beige adipocytes and played a key role in thermogenesis and metabolism.
Brown and beige adipose tissues dissipate chemical energy in the form of heat to maintain your body temperature in cold conditions. The impaired function of these tissues results in various metabolic diseases in humans and mice. By bioinformatical analyses, we identified a functional thermogenic regulator of adipose tissue, Androgen-dependent tissue factor pathway inhibitor [TFPI]-regulating protein (Adtrp), which was significantly overexpressed in and functionally activated the mature brown/beige adipocytes. Hereby, we knocked out Adtrp in mice which led to multiple abnormalities in thermogenesis, metabolism, and maturation of brown/beige adipocytes causing excess lipid accumulation in brown adipose tissue (BAT) and cold intolerance. The capability of thermogenesis in brown/beige adipose tissues could be recovered in Adtrp KO mice upon direct beta 3-adrenergic receptor (beta 3-AR) stimulation by CL316,243 treatment. Our mechanistic studies revealed that Adtrp by binding to S100 calcium-binding protein b (S100b) indirectly mediated the secretion of S100b, which in turn promoted the beta 3-AR mediated thermogenesis via sympathetic innervation. These results may provide a novel insight into Adtrp in metabolism via regulating the differentiation and thermogenesis of adipose tissues in mice.
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