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Aster-B–dependent estradiol synthesis protects female mice from diet-induced obesity
Xu Xiao, … , John W.R. Schwabe, Peter Tontonoz
Xu Xiao, … , John W.R. Schwabe, Peter Tontonoz
Published January 4, 2024
Citation Information: J Clin Invest. 2024;134(4):e173002. https://doi.org/10.1172/JCI173002.
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Research Article Metabolism

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

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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.

Authors

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

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Figure 3

Estradiol synthesis is impaired in Aster-B–KO mice.

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Estradiol synthesis is impaired in Aster-B–KO mice.
(A) Ovary weights fr...
(A) Ovary weights from female WT and Aster-B–KO mice after 10 weeks of WD feeding; n = 9 WT and 14 Aster-B–KO mice. (B–E) Representative stained sections for H&E (B), GDP9(C), BMP15 (D), and Cleaved Caspase3 (E) of ovaries from female WT and Aster-B–KO mice. Oocytes in the H&E staining are indicated by the arrow (12 in WT, 9 in Aster-B KO). (F) Expression levels of the indicated genes in the ovaries of WT and Aster-B–KO mice. n = 11 WT and 13 Aster-B–KO mice. (G–I) Plasma estradiol (G), LH (H) and FSH (I) from female WT and Aster-B–KO mice. n = 8 WT and 13 Aster-B–KO mice for estradiol; n = 10 WT and 12 Aster-B–KO mice for LH; n = 10 WT and 11 Aster-B–KO mice for FSH. (J and K) Body lean mass from female mice measured by MRI in chow diet (J) or after 10 weeks of WD feeding (K). n = 13 WT and 13 Aster-B–KO mice for chow diet; n = 11 WT and 15 Aster-B–KO mice for WD. (L and M) Body lean mass from male mice measured by MRI on chow diet (L) or after 10 weeks of WD feeding (M). n = 8 WT and 14 Aster-B–KO mice for chow diet; n = 9 WT and 11 Aster-B–KO mice for WD. All data are presented as mean ± SEM. P values were determined by 2-sided Student’s t test (A, F, G, H, I, J, K, L and M). *P < 0.05, **P < 0.01, ***P < 0.001, *****P < 0.00001

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