Computational analysis of liquid chromatography-tandem mass spectrometric steroid profiling in NCI H295R cells following angiotensin II, forskolin and abiraterone treatment. Issue 155 (January 2016)

• Record Type: Journal Article
• Authors: Mangelis, Anastasios; Dieterich, Peter; Peitzsch, Mirko; Richter, Susan; Jühlen, Ramona; Hübner, Angela; Willenberg, Holger S.; Deussen, Andreas; Lenders, Jacques W.M.; Eisenhofer, Graeme
• Is Part Of: Journal of steroid biochemistry and molecular biology. Issue 155 Part A(2016)
• Page Start: 67
• Page End: 75
• Publication Date: 2016-01
• Subjects: StAR steroidogenic acute regulatory protein -- CYP11A1 cholesterol side-chain cleavage enzyme -- CYP17 17-alpha-hydroxylase/17, 20-lyase -- 3β -HSD 3-beta-hydroxysteroid dehydrogenase -- CYP21A1 21 hydroxylase -- CYP11B1 11-beta-hydroxylase -- CYP11B2 aldosterone synthase -- RMSE root mean square error -- DHEA dehydroepiandrosterone; Computational analysis -- Steroidogenesis -- Steroid profiling -- LC–MS/MS; Steroid hormones -- Periodicals; Biochemistry -- Periodicals; Hormones -- Periodicals; Molecular Biology -- Periodicals; Hormones stéroïdes -- Périodiques; Steroid hormones; Periodicals; 572.579
• DOI: 10.1016/j.jsbmb.2015.09.038
• Languages: English
• ISSNs: 0960-0760

Abstract

Highlights: An LC–MS/MS based computational analysis of steroidogenesis is proposed. Multiple time point measurements reveal dynamics of induced perturbations. The computational analysis successfully describes steroid production. Calculated reaction rate constants appropriately reflect effects of agents. Abstract: Adrenal steroid hormones, which regulate a plethora of physiological functions, are produced via tightly controlled pathways. Investigations of these pathways, based on experimental data, can be facilitated by computational modeling for calculations of metabolic rate alterations. We therefore used a model system, based on mass balance and mass reaction equations, to kinetically evaluate adrenal steroidogenesis in human adrenal cortex-derived NCI H295R cells. For this purpose a panel of 10 steroids was measured by liquid chromatographic-tandem mass spectrometry. Time-dependent changes in cell incubate concentrations of steroids – including cortisol, aldosterone, dehydroepiandrosterone and their precursors – were measured after incubation with angiotensin II, forskolin and abiraterone. Model parameters were estimated based on experimental data using weighted least square fitting. Time-dependent angiotensin II- and forskolin-induced changes were observed for incubate concentrations of precursor steroids with peaks that preceded maximal increases in aldosterone and cortisol. Inhibition of 17-alpha-hydroxylase/17, 20-lyase with abiraterone resulted in increases in upstream precursor steroids and decreases in downstream products. Derived model parameters, including rate constants of enzymatic processes, appropriately quantified observed and expected changes in metabolic pathways at multiple conversion steps. Our data demonstrate limitations of single time point measurements and the importance of assessing pathway dynamics in studies of adrenal cortical cell line steroidogenesis. Our analysis provides a framework for evaluation of steroidogenesis in adrenal cortical cell culture systems and demonstrates that computational modeling-derived estimates of kinetic parameters are an effective tool for describing perturbations in associated metabolic pathways.