Aster-B–dependent estradiol synthesis protects female mice from diet-induced obesity

  • Xu Xiao
  • , John P. Kennelly
  • , An Chieh Feng
  • , Lijing Cheng
  • , Beatriz Romartinez-Alonso
  • , Alexander Bedard
  • , Yajing Gao
  • , Liujuan Cui
  • , Stephen G. Young
  • , John W.R. Schwabe
  • , Peter Tontonoz

Research output: Contribution to journalArticlepeer-review

11 Scopus citations

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 languageEnglish
Article number173002
JournalJournal of Clinical Investigation
Volume134
Issue number4
DOIs
StatePublished - 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.

FundersFunder number
Mark Foundation for Cancer ResearchDRG2424-21
National Institutes of Health (NIH)P01 HL146358, R01 DK126779
National Institutes of Health (NIH)
American the American Heart Association18Post34030388, 903306
American the American Heart Association
Damon Runyon Cancer Research Foundation
Fondation Leducq19CVD04
Fondation Leducq

    ASJC Scopus subject areas

    • General Medicine

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