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Publication : <i>Ire1α</i> in <i>Pomc</i> Neurons Is Required for Thermogenesis and Glycemia.

First Author  Yao T Year  2017
Journal  Diabetes Volume  66
Issue  3 Pages  663-673
PubMed ID  28028078 Mgi Jnum  J:246084
Mgi Id  MGI:5924323 Doi  10.2337/db16-0533
Citation  Yao T, et al. (2017) Ire1alpha in Pomc Neurons Is Required for Thermogenesis and Glycemia. Diabetes 66(3):663-673
abstractText  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 Ire1alpha 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 Ire1alpha in Pomc neurons impaired whole-body glucose and insulin tolerance as well as hepatic insulin sensitivity. At the cellular level, deletion of Ire1alpha 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 Ire1alpha-Xbp1s and associated molecular targets link ER stress in arcuate Pomc neurons to aspects of normal energy and glucose homeostasis.
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