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Critical roles of nardilysin in the maintenance of body temperature homoeostasis.


ABSTRACT: Body temperature homoeostasis in mammals is governed centrally through the regulation of shivering and non-shivering thermogenesis and cutaneous vasomotion. Non-shivering thermogenesis in brown adipose tissue (BAT) is mediated by sympathetic activation, followed by PGC-1? induction, which drives UCP1. Here we identify nardilysin (Nrd1 and NRDc) as a critical regulator of body temperature homoeostasis. Nrd1(-/-) mice show increased energy expenditure owing to enhanced BAT thermogenesis and hyperactivity. Despite these findings, Nrd1(-/-) mice show hypothermia and cold intolerance that are attributed to the lowered set point of body temperature, poor insulation and impaired cold-induced thermogenesis. Induction of ?3-adrenergic receptor, PGC-1? and UCP1 in response to cold is severely impaired in the absence of NRDc. At the molecular level, NRDc and PGC-1? interact and co-localize at the UCP1 enhancer, where NRDc represses PGC-1? activity. These findings reveal a novel nuclear function of NRDc and provide important insights into the mechanism of thermoregulation.

SUBMITTER: Hiraoka Y 

PROVIDER: S-EPMC3926010 | biostudies-literature | 2014

REPOSITORIES: biostudies-literature

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Body temperature homoeostasis in mammals is governed centrally through the regulation of shivering and non-shivering thermogenesis and cutaneous vasomotion. Non-shivering thermogenesis in brown adipose tissue (BAT) is mediated by sympathetic activation, followed by PGC-1α induction, which drives UCP1. Here we identify nardilysin (Nrd1 and NRDc) as a critical regulator of body temperature homoeostasis. Nrd1(-/-) mice show increased energy expenditure owing to enhanced BAT thermogenesis and hypera  ...[more]

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