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Pirt deficiency has subtle female-specific effects on energy and glucose metabolism in mice.
Mol. Metab. 23, 75-81 (2019)
Objective: The contribution of brown adipose tissue (BAT) to adult human metabolic control is a topic of ongoing investigation. In context, understanding the cellular events leading to BAT uncoupling, heat production, and energy expenditure is anticipated to produce significant insight into this endeavor. The phosphoinositide interacting regulator of transient receptor potentials (Pirt) was recently put forward as a key protein regulating cold sensing downstream of the transient receptor potential melastatin 8 (TRPM8). Notably, TRPM8 has been identified as a non-canonical regulator of BAT thermogenesis. The aim of this investigation was to delineate the role of Pirt in energy homeostasis and glucose metabolism - and the possible involvement of Pirt in TRPM8-elicited energy expenditure.Methods: To this end, we metabolically phenotyped male and female Pirt deficient (Pirt(-/-)) mice exposed to a low-fat chow diet or to a high-fat, high-sugar (HFHS) diet.Results: We identified that chow-fed female Pirt(-/-) mice have an increased susceptibility to develop obesity and glucose intolerance. This effect is abrogated when the mice are exposed to a HFHS diet. Conversely, Pirt(-/-) male mice display no metabolic phenotype on either diet relative to wild-type (WT) control mice. Finally, we observed that Pirt is dispensable for TRPM8-evoked energy expenditure.Conclusion: We here report subtle metabolic abnormalities in female, but not male, Pirt(-/-) mice. Future studies are required to tease out if metabolic stressors beyond dietary interventions, e.g. temperature fluctuations, are interacting with Pirt-signaling and metabolic control in a sex-specific fashion.
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Publikationstyp
Artikel: Journalartikel
Dokumenttyp
Wissenschaftlicher Artikel
Schlagwörter
Signaling Molecule ; Sex Differences ; Body Weight ; Energy Metabolism ; Trpm8 ; Brown Adipose Tissue; Brown Adipose-tissue; Identification; Adipocytes; Activation; Induction; Channels; Protein
ISSN (print) / ISBN
2212-8778
e-ISSN
2212-8778
Zeitschrift
Molecular Metabolism
Quellenangaben
Band: 23,
Seiten: 75-81
Verlag
Elsevier
Verlagsort
Amsterdam
Nichtpatentliteratur
Publikationen
Begutachtungsstatus
Peer reviewed
Institut(e)
Institute of Diabetes and Obesity (IDO)