Contrasting recruitment of skin‐associated adipose depots during cold challenge of mouse and human

Key points Several distinct strategies produce and conserve heat to maintain the body temperature of mammals, each associated with unique physiologies, with consequences for wellness and disease susceptibility Highly regulated properties of skin offset the total requirement for heat production  We h...

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Published inThe Journal of physiology Vol. 600; no. 4; pp. 847 - 868
Main Authors Kasza, Ildiko, Kühn, Jens‐Peter, Völzke, Henry, Hernando, Diego, Xu, Yaohui G., Siebert, John W., Gibson, Angela L. F., Yen, C. ‐L. Eric, Nelson, David W., MacDougald, Ormond A., Richardson, Nicole E., Lamming, Dudley W., Kern, Philip A., Alexander, C. M.
Format Journal Article
LanguageEnglish
Published England Wiley Subscription Services, Inc 01.02.2022
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Summary:Key points Several distinct strategies produce and conserve heat to maintain the body temperature of mammals, each associated with unique physiologies, with consequences for wellness and disease susceptibility Highly regulated properties of skin offset the total requirement for heat production  We hypothesize that the adipose component of skin is primarily responsible for modulating heat flux; here we evaluate the relative regulation of adipose depots in mouse and human, to test their recruitment to heat production and conservation We found that insulating mouse dermal white adipose tissue accumulates in response to environmentally and genetically induced cool stress; this layer is one of two adipose depots closely apposed to mouse skin, where the subcutaneous mammary gland fat pads are actively recruited to heat production In contrast, the body‐wide adipose depot associated with human skin produces heat directly, potentially creating an alternative to the centrally regulated brown adipose tissue Mammalian skin impacts metabolic efficiency system‐wide, controlling the rate of heat loss and consequent heat production. Here we compare the unique fat depots associated with mouse and human skin, to determine whether they have corresponding functions and regulation. For humans, we assay a skin‐associated fat (SAF) body‐wide depot to distinguish it from the subcutaneous fat pads characteristic of the abdomen and upper limbs. We show that the thickness of SAF is not related to general adiposity; it is much thicker (1.6‐fold) in women than men, and highly subject‐specific. We used molecular and cellular assays of β‐adrenergic‐induced lipolysis and found that dermal white adipose tissue (dWAT) in mice is resistant to lipolysis; in contrast, the body‐wide human SAF depot becomes lipolytic, generating heat in response to β‐adrenergic stimulation. In mice challenged to make more heat to maintain body temperature (either environmentally or genetically), there is a compensatory increase in thickness of dWAT: a corresponding β‐adrenergic stimulation of human skin adipose (in vivo or in explant) depletes adipocyte lipid content. We summarize the regulation of skin‐associated adipocytes by age, sex and adiposity, for both species. We conclude that the body‐wide dWAT depot of mice shows unique regulation that enables it to be deployed for heat preservation; combined with the actively lipolytic subcutaneous mammary fat pads they enable thermal defence. The adipose tissue that covers human subjects produces heat directly, providing an alternative to the brown adipose tissues.
Bibliography:https://doi.org/10.1101/2020.09.16.300533v2
This article was first published as a preprint. Kasza L, Kühn J‐P, Völzke H, Hernando D, Xu YG, Siebert JW, Gibson ALF, Yen C‐L E, Nelson DW, MacDougald OA, Richardson NE, Lamming DW, Kern PA, Alexander CM. 2021. Contrasting recruitment of skin‐associated adipose depots during cold challenge of mouse and human. bioRxiv.
Edited by: Kim Barrett & Yasuhiko Minokoshi
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CMA Development of strategy, execution of experimental procedures, consultation with analysis, manuscript preparation; IK Design and execution of experimental procedures, data analysis and presentation, manuscript preparation; JK, HZ, RB, DH Design and execution of MRI imaging procedures, data analysis and presentation; AG, YZ, JS, PK Collection of human skin and fat samples; CLEY, DN, NR, DL Development of strategy, consultation on mouse metabolic studies, supply of samples from mice on high fat feeding protocols; OM Development of strategy, manuscript preparation. All authors approved the final version of this manuscript and agree to be accountable for the accuracy and integrity of the work.
Author contributions
ISSN:0022-3751
1469-7793
DOI:10.1113/JP280922