Liimatta, Jani Petri TapaniJani Petri TapaniLiimattaCurschellas, Evelyn CathrineEvelyn CathrineCurschellasAltinkiliç, Emre MuratEmre MuratAltinkiliçNa'Amneh Elzenaty, RawdaRawdaNa'Amneh ElzenatyAugsburger, Philipp EmanuelPhilipp EmanuelAugsburgerDu Toit, TherinaTherinaDu ToitVögel, ClarissaClarissaVögelBreault, David TDavid TBreaultFlück Pandey, Christa EmmaChrista EmmaFlück Pandey0000-0002-4568-5504Pignatti, EmanueleEmanuelePignatti2024-10-262024-10-262024-01-16https://boris-portal.unibe.ch/handle/20.500.12422/173964Cholesterol is the precursor of all steroids, but how cholesterol flux is controlled in steroidogenic tissues is poorly understood. The cholesterol exporter ABCG1 is an essential component of the reverse cholesterol pathway and its global inactivation results in neutral lipid redistribution to tissue macrophages. The function of ABCG1 in steroidogenic tissues, however, has not been explored. To model this, we inactivated Abcg1 in the mouse adrenal cortex, which led to an adrenal-specific increase in transcripts involved in cholesterol uptake and de novo synthesis. Abcg1 inactivation did not affect adrenal cholesterol content, zonation, or serum lipid profile. Instead, we observed a moderate increase in corticosterone production that was not recapitulated by the inactivation of the functionally similar cholesterol exporter Abca1. Altogether, our data imply that Abcg1 controls cholesterol uptake and biosynthesis and regulates glucocorticoid production in the adrenal cortex, introducing the possibility that ABCG1 variants may account for physiological or subclinical variation in stress response.enAbcg1 adrenal cortex cholesterol glucocorticoids steroids600 - Technology::610 - Medicine & healtharticle10.48350/1923493830127110.1210/endocr/bqae014