4.7 Article

Epidermal Acyl-CoA-binding protein is indispensable for systemic energy homeostasis

Journal

MOLECULAR METABOLISM
Volume 44, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.molmet.2020.101144

Keywords

Epidermal barrier; Energy expenditure; Adipose tissue; Browning; Diet induced obesity; beta-adrenergic signaling; Acyl-CoA binding protein; Filaggrin

Funding

  1. Independent Research Fund Denmark - Natural Sciences
  2. Novo Nordisk Foundation
  3. Lundbeck Foundation
  4. VILLUM Foundation through a grant to the VILLUM Center for Bioanalytical Sciences at the University of Southern Denmark
  5. NordForsk through a grant to the Nordic Center of Excellence MitoHealth

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The loss of ACBP in keratinocytes leads to increased energy expenditure, food intake, browning of adipose tissue, and resistance to diet-induced obesity. These findings highlight the crucial role of the epidermal barrier in maintaining systemic metabolic homeostasis.
Objectives: The skin is the largest sensory organ of the human body and plays a fundamental role in regulating body temperature. However, adaptive alterations in skin functions and morphology have only vaguely been associated with physiological responses to cold stress or sensation of ambient temperatures. We previously found that loss of acyl-CoA-binding protein (ACBP) in keratinocytes upregulates lipolysis in white adipose tissue and alters hepatic lipid metabolism, suggesting a link between epidermal barrier functions and systemic energy metabolism. Methods: To assess the physiological responses to loss of ACBP in keratinocytes in detail, we used full-body ACBP(-/-) and skin-specific ACBP(-/-) knockout mice to clarify how loss of ACBP affects 1) energy expenditure by indirect calorimetry, 2) response to high-fat feeding and a high oral glucose load, and 3) expression of brown-selective gene programs by quantitative PCR in inguinal WAT (iWAT). To further elucidate the role of the epidermal barrier in systemic energy metabolism, we included mice with defects in skin structural proteins (ma/ma Flg(ft/ft)) in these studies. Results: We show that the ACBP(-/-) mice and skin-specific ACBP(-/-) knockout mice exhibited increased energy expenditure, increased food intake, browning of the iWAT, and resistance to diet-induced obesity. The metabolic phenotype, including browning of the iWAT, was reversed by housing the mice at thermoneutrality (30 degrees C) or pharmacological beta-adrenergic blocking. Interestingly, these findings were phenocopied in flaky tail mice (ma/ma Flg(ft/ft)). Taken together, we demonstrate that a compromised epidermal barrier induces a beta-adrenergic response that increases energy expenditure and browning of the white adipose tissue to maintain a normal body temperature. Conclusions: Our findings show that the epidermal barrier plays a key role in maintaining systemic metabolic homeostasis. Thus, regulation of epidermal barrier functions warrants further attention to understand the regulation of systemic metabolism in further detail. (C) 2020 The Author(s). Published by Elsevier GmbH.

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