HSDL2 links nutritional cues to bile acid and cholesterol homeostasis

• Published in: Science advances Vol. 10; no. 22; p. eadk9681
• Main Authors: Samson, Nolwenn, Bosoi, Cristina R., Roy, Christian, Turcotte, Laurie, Tribouillard, Laura, Mouchiroud, Mathilde, Berthiaume, Line, Trottier, Jocelyn, Silva, Heitor C. G., Guerbette, Thomas, Plata-Gómez, Ana Belén, Besse-Patin, Aurèle, Montoni, Alicia, Ilacqua, Nicolò, Lamothe, Jennifer, Citron, Yemima R., Gélinas, Yves, Gobeil, Stéphane, Zoncu, Roberto, Caron, Alexandre, Morissette, Mathieu, Pellegrini, Luca, Rochette, Patrick J., Estall, Jennifer L., Efeyan, Alejo, Shum, Michael, Audet-Walsh, Étienne, Barbier, Olivier, Marette, André, Laplante, Mathieu
• Format: Journal Article
• Language: English
• Published: United States 31.05.2024
• Subjects: Animals; Bile Acids and Salts - metabolism; Cholesterol - metabolism; Fasting - metabolism; Hepatocytes - metabolism; Homeostasis; Humans; Hydroxysteroid Dehydrogenases - genetics; Hydroxysteroid Dehydrogenases - metabolism; Liver - metabolism; Mechanistic Target of Rapamycin Complex 1 - metabolism; Mice; Mitochondria - metabolism; Signal Transduction
• ISSN: 2375-2548; 2375-2548
• DOI: 10.1126/sciadv.adk9681

In response to energy and nutrient shortage, the liver triggers several catabolic processes to promote survival. Despite recent progress, the precise molecular mechanisms regulating the hepatic adaptation to fasting remain incompletely characterized. Here, we report the identification of hydroxysteroid dehydrogenase–like 2 (HSDL2) as a mitochondrial protein highly induced by fasting. We show that the activation of PGC1α-PPARα and the inhibition of the PI3K-mTORC1 axis stimulate HSDL2 expression in hepatocytes. We found that HSDL2 depletion decreases cholesterol conversion to bile acids (BAs) and impairs FXR activity. HSDL2 knockdown also reduces mitochondrial respiration, fatty acid oxidation, and TCA cycle activity. Bioinformatics analyses revealed that hepatic Hsdl2 expression positively associates with the postprandial excursion of various BA species in mice. We show that liver-specific HSDL2 depletion affects BA metabolism and decreases circulating cholesterol levels upon refeeding. Overall, our report identifies HSDL2 as a fasting-induced mitochondrial protein that links nutritional signals to BAs and cholesterol homeostasis. HSDL2 is a mitochondrial protein that controls bile acid and lipid metabolism in response to nutritional cues.