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Plasma membrane cholesterol trafficking in steroidogenesis.

Citation
Deng, B., et al. “Plasma Membrane Cholesterol Trafficking In Steroidogenesis.”. Faseb Journal : Official Publication Of The Federation Of American Societies For Experimental Biology, pp. 1389-1400.
Center Stanford University
Author Bing Deng, Wen-Jun Shen, Dachuan Dong, Salman Azhar, Fredric B Kraemer
Keywords SNARE proteins, adrenal gland, mitochondria
Abstract

Cholesterol is an important component of plasma membranes (PMs) and the precursor of all steroid hormones. In steroidogenic tissues, upon hormone stimulation, there is a rapid transfer of cholesterol to the mitochondria, which is the site of the initial step in steroidogenesis. In the current study, we examined PM cholesterol trafficking for steroidogenesis. In a mitochondrial reconstitution assay, adrenal PMs supported steroidogenesis in the absence of additional transport proteins. Depletion of cholesterol in PMs by 50% eliminated the membranes' ability to support steroidogenesis in vitro and reduced steroid production in intact Y1 adrenocortical cells. Syntaxin (STX)-5 and α-soluble N-ethylmaleimide-sensitive factor attachment protein (α-SNAP) are enriched in adrenal PMs, and adrenocorticotropic hormone treatment of rats recruited STX5 and α-SNAP to adrenal PMs and mitochondria. Immunodepletion of STX5 and α-SNAP from PMs decreased steroidogenesis supported by PMs in vitro. Protease digestion of PMs decreased, whereas recombinant STX5 or α-SNAP restored, the PMs' ability to support steroidogenesis. Knockdown of either STX5 or α-SNAP in Y1 cells decreased stimulated steroidogenesis. These results indicate that STX5 and α-SNAP facilitate cholesterol trafficking from PMs to mitochondria for adrenal steroid synthesis and underscore the importance of vesicular trafficking of PM cholesterol for steroidogenesis.-Deng, B., Shen, W.-J., Dong, D., Azhar, S., Kraemer, F. B. Plasma membrane cholesterol trafficking in steroidogenesis.

Year of Publication
2019
Journal
FASEB journal : official publication of the Federation of American Societies for Experimental Biology
Volume
33
Issue
1
Number of Pages
1389-1400
Date Published
12/2019
ISSN Number
1530-6860
DOI
10.1096/fj.201800697RRR
Alternate Journal
FASEB J.
PMID
30133326
PMCID
PMC6988844
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