Abstract
Aster proteins mediate the nonvesicular transport of cholesterol from the plasma membrane (PM) to the endoplasmic reticulum (ER). However, the importance of nonvesicular sterol movement for physiology and pathophysiology in various tissues is incompletely understood. Here we show that loss of Aster-B leads to diet-induced obesity in female but not in male mice, and that this sex difference is abolished by ovariectomy. We further demonstrate that Aster-B deficiency impairs nonvesicular cholesterol transport from the PM to the ER in ovaries in vivo, leading to hypogonadism and reduced estradiol synthesis. Female Aster-B–deficient mice exhibit reduced locomotor activity and energy expenditure, consistent with established effects of estrogens on systemic metabolism. Administration of exogenous estradiol ameliorates the diet-induced obesity phenotype of Aster-B–deficient female mice. These findings highlight the key role of Aster-B–dependent nonvesicular cholesterol transport in regulating estradiol production and protecting females from obesity.
| Original language | English |
|---|---|
| Article number | 173002 |
| Journal | Journal of Clinical Investigation |
| Volume | 134 |
| Issue number | 4 |
| DOIs | |
| State | Published - Feb 15 2024 |
Bibliographical note
Publisher Copyright:© 2024, Xiao et al. This is an open access article published under the terms of the Creative Commons Attribution 4.0 International License.
Funding
We thank Yuta Shimannaka and all members of the Tontonoz laboratory at UCLA for useful advice and discussions. We thank Stephen T. Smale (UCLA), Nazim Mohammad (UCLA), Wen Xiao (UCLA), and Ya (Allen) Cui (UCI) for their invaluable sup- port and discussions. This work was supported by NIH grants P01 HL146358, R01 DK126779, and Fondation Leducq Transatlantic Network of Excellence (19CVD04). XX was supported by AHA Postdoctoral Fellowship (18Post34030388). JPK was supported by AHA Postdoctoral Fellowship (903306). YG was supported by Damon Runyon Cancer Research Foundation and Mark Foundation postdoctoral fellowship (DRG2424-21). Confocal microscopy was performed at the California NanoSystems Institute of Advanced Light Microscopy/ Spectroscopy Facility. Histology analysis was performed at the UCLA Translational Pathology Core Laboratory.
| Funders | Funder number |
|---|---|
| Mark Foundation for Cancer Research | DRG2424-21 |
| National Institutes of Health (NIH) | P01 HL146358, R01 DK126779 |
| National Institutes of Health (NIH) | |
| American the American Heart Association | 18Post34030388, 903306 |
| American the American Heart Association | |
| Damon Runyon Cancer Research Foundation | |
| Fondation Leducq | 19CVD04 |
| Fondation Leducq |
ASJC Scopus subject areas
- General Medicine