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NBR1 is a critical step in the repression of thermogenesis of p62-deficient adipocytes through PPARγ
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NBR1 is a critical step in the repression of thermogenesis of p62-deficient adipocytes through PPARγ
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Journal Article
NBR1 is a critical step in the repression of thermogenesis of p62-deficient adipocytes through PPARγ
2021
Overview
Activation of non-shivering thermogenesis is considered a promising approach to lower body weight in obesity. p62 deficiency in adipocytes reduces systemic energy expenditure but its role in sustaining mitochondrial function and thermogenesis remains unresolved. NBR1 shares a remarkable structural similarity with p62 and can interact with p62 through their respective PB1 domains. However, the physiological relevance of NBR1 in metabolism, as compared to that of p62, was not clear. Here we show that whole-body and adipocyte-specific ablation of NBR1 reverts the obesity phenotype induced by p62 deficiency by restoring global energy expenditure and thermogenesis in brown adipose tissue. Impaired adrenergic-induced browning of p62-deficient adipocytes is rescued by NBR1 inactivation, unveiling a negative role of NBR1 in thermogenesis under conditions of p62 loss. We demonstrate that upon p62 inactivation, NBR1 represses the activity of PPARγ, establishing an unexplored p62/NBR1-mediated paradigm in adipocyte thermogenesis that is critical for the control of obesity.
p62 is a signaling hub protein that contributes to the control of energy expenditure. Here the authors investigate the relative roles of p62 and a similar protein, NBR1, and show that NBR1 is required for the repression of thermogenesis in adipocytes occurring in the absence of p62.
Publisher
Nature Publishing Group UK,Nature Publishing Group,Nature Portfolio
Subject
/ 13/106
/ 13/109
/ 13/44
/ 13/51
/ 13/95
/ 38/22
/ 38/77
/ 38/88
/ 64/60
/ 82/1
/ 82/29
/ 82/80
/ Ablation
/ Adipose Tissue, Brown - cytology
/ Adipose Tissue, Brown - metabolism
/ Animals
/ Browning
/ Energy Metabolism - genetics
/ Humanities and Social Sciences
/ Humans
/ Intracellular Signaling Peptides and Proteins - deficiency
/ Intracellular Signaling Peptides and Proteins - genetics
/ Mice
/ Obesity
/ Proteins
/ Retinoid X Receptor alpha - genetics
/ Retinoid X Receptor alpha - metabolism
/ Science
/ Sequestosome-1 Protein - deficiency
