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Brown and beige fat in humans: thermogenic adipocytes that control energy and glucose homeostasis
Labros Sidossis, Shingo Kajimura
Labros Sidossis, Shingo Kajimura
Published February 2, 2015
Citation Information: J Clin Invest. 2015;125(2):478-486. https://doi.org/10.1172/JCI78362.
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Review

Brown and beige fat in humans: thermogenic adipocytes that control energy and glucose homeostasis

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Abstract

Brown adipose tissue (BAT), a specialized fat that dissipates energy to produce heat, plays an important role in the regulation of energy balance. Two types of thermogenic adipocytes with distinct developmental and anatomical features exist in rodents and humans: classical brown adipocytes and beige (also referred to as brite) adipocytes. While classical brown adipocytes are located mainly in dedicated BAT depots of rodents and infants, beige adipocytes sporadically reside with white adipocytes and emerge in response to certain environmental cues, such as chronic cold exposure, a process often referred to as “browning” of white adipose tissue. Recent studies indicate the existence of beige adipocytes in adult humans, making this cell type an attractive therapeutic target for obesity and obesity-related diseases, including type 2 diabetes. This Review aims to cover recent progress in our understanding of the anatomical, developmental, and functional characteristics of brown and beige adipocytes and discuss emerging questions, with a special emphasis on adult human BAT.

Authors

Labros Sidossis, Shingo Kajimura

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Figure 3

External and internal factors that regulate beige adipocyte development under lean and obese conditions.

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External and internal factors that regulate beige adipocyte development ...
Beige adipocyte development is induced by the indicated stimuli and mediated by the listed endocrine factors. This process is associated with increased energy expenditure, reduced body weight, and improved insulin sensitivity. Under obese conditions, beige adipocyte development is impaired through multiple factors, including but not limited to reduced sympathetic nervous system (SNS) activity and increased activation of signaling pathways that inhibit beige adipocyte development. Impaired beige adipocyte development is associated with reduced energy expenditure, increased body weight, reduced insulin sensitivity, and development of hepatic steatosis.

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