Key result
CLSTN3b is significantly enriched in human multilocular brown perirenal fat compared to subcutaneous white fat and positively correlates with UCP1 expression.
p-value: p=<0.01
CLSTN3b serves as a hallmark of thermogenic adipose depots in both mice and humans, responding dynamically to temperature and obesity.
Hypothesis-generating for human brown fat biology; leaves open any metabolic role pending validation studies.
Activation of thermogenic adipose tissue is linked to improved metabolic outcomes in mice and humans. Dissipation of energy as heat during thermogenesis relies on sufficient innervation of fat by sympathetic nerve fibers, a process recently proposed to be regulated by the adipose-specific Calsyntenin3b (Clstn3b)-S100b axis. Here we aimed 1) to assess enrichment patterns of CLSTN3b, S100b as well as the previously annotated neuronal CLSTN3a in perirenal brown and subcutaneous white human fat specimens, and 2) to investigate if the novel Clstn3b is dynamically regulated by changes in environmental temperatures and nutritional stress in thermogenic adipose tissues in mice. We provide evidence for CLSTN3b enrichment in multilocular perirenal fat located anatomically in the proximity to both the adrenal gland and sympathetic nerve bundles innervating the kidney in humans. Moreover, transcript levels of CLSTN3b, but not S100b or CLSTN3a, positively correlate with uncoupling protein 1 (UCP1) expression in human adipose tissue. Our results further show that Clsnt3b is preferentially expressed in brown adipocytes and is highly responsive to changes in environmental temperature and obesity state in mice. Collectively, this brief communication highlights CLSTN3b as a hallmark of thermogenic adipose depots in mice and humans.
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Plucińska et al. (2020) studied Healthy kidney donors (n=16). Multilocular perirenal brown adipose tissue vs. Subcutaneous white adipose tissue was evaluated on CLSTN3b transcript enrichment (p=<0.01). CLSTN3b is significantly enriched in human multilocular brown perirenal fat compared to subcutaneous white fat and positively correlates with UCP1 expression.
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