Adrenal Abcg1 Controls Cholesterol Flux and Steroidogenesis

Author:

Liimatta Jani123ORCID,Curschellas Evelyn4,Altinkilic Emre Murat12,Naamneh Elzenaty Rawda2,Augsburger Philipp2,du Toit Therina125,Voegel Clarissa D25,Breault David T67,Flück Christa E12,Pignatti Emanuele12ORCID

Affiliation:

1. Division of Pediatric Endocrinology, Diabetology and Metabolism, Department of Pediatrics, Inselspital, Bern University Hospital , Bern 3010 , Switzerland

2. Department for BioMedical Research, University Hospital Inselspital, University of Bern , Bern 3010 , Switzerland

3. Kuopio Pediatric Research Unit (KuPRU), University of Eastern Finland and Kuopio University Hospital , Kuopio 70200 , Finland

4. Department of Chemistry, Biochemistry and Pharmacy, Medical Faculty, University of Bern , Bern 3010 , Switzerland

5. Department of Nephrology and Hypertension, Inselspital, Bern University Hospital, University of Bern , Bern 3010 , Switzerland

6. Department of Pediatrics, Harvard Medical School, Boston Children's Hospital , Boston, MA 02115 , USA

7. Harvard Stem Cell Institute , Cambridge, MA 02138 , USA

Abstract

Abstract Cholesterol 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.

Funder

Novartis Foundation for Medical-Biological Research

NCCR RNA&Disease Translational Fellowship Grant

International Fund Congenital Adrenal Hyperplasia

University of Bern via the Initiator

Uniscientia Foundation Zürich/Vaduz

Sigrid Jusélius Foundation

Foundation for Pediatric Research

Publisher

The Endocrine Society

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