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. 2018 Nov;78(1):e65.
doi: 10.1002/cptx.65. Epub 2018 Oct 15.

Assessment of Altered Cholesterol Homeostasis by Xenobiotics Using Ultra-High Performance Liquid Chromatography-Tandem Mass Spectrometry

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Assessment of Altered Cholesterol Homeostasis by Xenobiotics Using Ultra-High Performance Liquid Chromatography-Tandem Mass Spectrometry

Josi Herron et al. Curr Protoc Toxicol. 2018 Nov.

Abstract

Cholesterol and cholesterol-derived oxysterols are critical for embryonic development, synapse formation and function, and myelination, among other biological functions. Indeed, alterations in levels of cholesterol, sterol precursors, and oxysterols result in a variety of developmental disorders, emphasizing the importance of cholesterol homeostasis. The ability of xenobiotics to reproduce similar phenotypes by altering cholesterol homeostasis has increasingly become of interest. Therefore, the ability to quantitatively assess alterations in cholesterol homeostasis resulting from exposure to xenobiotics is of value. This unit describes methods for the quantitative assessment of altered post-squalene cholesterol biosynthesis and subsequent oxysterol formation in various sample types using ultra-high performance liquid chromatography-tandem mass spectrometry (UHPLC-MS/MS). Understanding alterations in cholesterol homeostasis resulting from xenobiotic exposure can provide key insight into the toxicant's mechanism of action and resulting phenotype. © 2018 by John Wiley & Sons, Inc.

Keywords: cholesterol; homeostasis; liquid chromatography-mass spectrometry; oxysterols; sterols; xenobiotics.

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Figures

Figure 1.
Figure 1.
Post-squalene cholesterol biosynthetic pathway and examples of malformation disorders associated with defects at specific steps.
Figure 2.
Figure 2.
Structures of the main cholesterol-derived oxysterols.
Figure 3.
Figure 3.
Representative image of aqueous (top), protein (thin, middle layer), and lipid (bottom) layers from a cell sample.
Figure 4.
Figure 4.
LC-MS chromatogram of the oxysterol standard sample, including the internal standard d7-7-ketocholesterol (peak S) and all oxysterol standards. Mass transitions are denoted in color legend.
Figure 5.
Figure 5.
LC-MS chromatogram of the sterol standard sample, including the internal standards 13C3-desmosterol, d7-7-DHC, d7-cholesterol, and 13C3-lanosterol (top panel) and all sterol standards (bottom panel). Mass transitions are denoted in color legend.

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