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Ire1? in Pomc Neurons Is Required for Thermogenesis and Glycemia.


ABSTRACT: Whether neuronal inositol-requiring enzyme 1 (Ire1) is required for the proper regulation of energy balance and glucose homeostasis is unclear. We found that pro-opiomelanocortin (Pomc)-specific deficiency of Ire1? accelerated diet-induced obesity concomitant with a decrease in energy expenditure. This hypometabolic phenotype included deficits in thermogenic responses to diet and cold exposure as well as "beiging" of white adipose tissue. We also demonstrate that loss of Ire1? in Pomc neurons impaired whole-body glucose and insulin tolerance as well as hepatic insulin sensitivity. At the cellular level, deletion of Ire1? in Pomc neurons elevated hypothalamic endoplasmic reticulum (ER) stress and predisposed Pomc neurons to leptin and insulin resistance. Together, the current studies extend and confirm conclusions that Ire1?-Xbp1s and associated molecular targets link ER stress in arcuate Pomc neurons to aspects of normal energy and glucose homeostasis.

SUBMITTER: Yao T 

PROVIDER: S-EPMC5319716 | biostudies-literature | 2017 Mar

REPOSITORIES: biostudies-literature

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Whether neuronal inositol-requiring enzyme 1 (<i>Ire1</i>) is required for the proper regulation of energy balance and glucose homeostasis is unclear. We found that pro-opiomelanocortin (<i>Pomc</i>)-specific deficiency of <i>Ire1α</i> accelerated diet-induced obesity concomitant with a decrease in energy expenditure. This hypometabolic phenotype included deficits in thermogenic responses to diet and cold exposure as well as "beiging" of white adipose tissue. We also demonstrate that loss of <i>  ...[more]

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