No extra-adrenal aldosterone production in various human cell lines.

IF 3.8 4区 医学 Q2 ENDOCRINOLOGY & METABOLISM
Journal of molecular endocrinology Pub Date : 2024-02-01 Print Date: 2024-04-01 DOI:10.1530/JME-23-0100
Isabelle Durrer, Daniel Ackermann, Rahel Klossner, Michael Grössl, Clarissa Vögel, Therina Du Toit, Bruno Vogt, Heidi Jamin, Markus G Mohaupt, Carine Gennari-Moser
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引用次数: 0

Abstract

Extra-adrenal de novo aldosterone (Aldo) production has been described inconsistently. Systematic data based upon state-of-the-art technology including validated controls are sparse. We hypothesized that aldosterone synthase (CYP11B2) expression and de novo Aldo production are absent in nonadrenal human cell lines, either immortalized cell lines or commercially available primary cell lines, including peripheral blood mononuclear cells (PBMCs) of individuals without and with primary hyperaldosteronism (PA). CYP11B2-transfected COS-7 and endogenous CYP11B2 expressing adrenal H295R cells served as positive controls. Various well-characterized, purchased, immortalized (BeWo, HEK293, HTR-8/SVneo, JEG-3) and primary (HAEC, HLEC, HRGEC, HRMC, HUAEC, HUVEC, PBMC) cell lines as well as self-isolated PBMCs from PA patients (n = 5) were incubated with the steroid hormone substrates progesterone, deoxycorticosterone, corticosterone or 18-OH-corticosterone with and without Ang II for 24 h to assess CYP11B2 enzymatic activity. CYP11B2 expression was analyzed by real-time PCR and liquid chromatography-mass spectrometry was used to quantify Aldo production. Pronounced CYP11B2 mRNA expression and Aldo production were observed in both positive controls, which followed an incremental time course. Neither substrates alone nor coincubation with Ang II significantly stimulated CYP11B2 expression or Aldo production in various immortalized and primary cell lines and PBMCs of PA patients. These results strongly support the absence of relevant de novo extra-adrenal Aldo production in nonadrenal cells, including blood mononuclear cells, irrespective of the absence or presence of autonomous adrenal Aldo production.

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在各种人类细胞系中均未产生肾上腺外醛固酮。
对肾上腺外新生醛固酮(Aldo)分泌的描述并不一致。基于最先进技术(包括经过验证的对照组)的系统数据非常稀少。我们假设醛固酮合成酶(CYP11B2)在非肾上腺人体细胞系(无论是永生细胞系还是市售原代细胞系,包括无原发性醛固酮增多症(PA)和原发性醛固酮增多症(PA)患者的外周血单核细胞(PBMCs))中没有表达和去原代醛固酮生成。CYP11B2 转染的 COS-7 细胞和内源性 CYP11B2 表达的肾上腺 H295R 细胞作为阳性对照。各种特征明确的、外购的永生化细胞系(BeWo、HEK293、HTR-8/SVneo、JEG-3)和原代细胞系(HAEC、HLEC、HRGEC、HRMC、HUAEC、HUVEC、PBMC)以及细胞培养方法(CYP11B2、CYP11B2-3、CYP11B2-4、CYP11B2-5、CYP11B2-6、CYP11B2-7)均可作为阳性对照、PBMC)细胞系以及 PA 患者自我分离的 PBMCs(n=5)与类固醇激素底物黄体酮、脱氧皮质酮、皮质酮或 18-OH- 皮质酮(有或无 Ang II)孵育 24 小时,以评估 CYP11B2 酶活性。实时 PCR 分析了 CYP11B2 的表达,液相色谱-质谱法(LC-MS)定量分析了 Aldo 的产生。在两个阳性对照中都观察到了明显的 CYP11B2 mRNA 表达和 Aldo 生成,其时间过程呈递增趋势。在各种永生细胞系、原代细胞系和 PA 患者的 PBMCs 中,无论是单独使用底物还是与 Ang II 共孵育,都不会明显刺激 CYP11B2 的表达或 Aldo 的产生。这些结果有力地证明了非肾上腺细胞(包括血液单核细胞)中不存在相关的肾上腺外Aldo生成,无论是否存在肾上腺自主Aldo生成。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of molecular endocrinology
Journal of molecular endocrinology 医学-内分泌学与代谢
CiteScore
6.90
自引率
0.00%
发文量
96
审稿时长
1 months
期刊介绍: The Journal of Molecular Endocrinology is an official journal of the Society for Endocrinology and is endorsed by the European Society of Endocrinology and the Endocrine Society of Australia. Journal of Molecular Endocrinology is a leading global journal that publishes original research articles and reviews. The journal focuses on molecular and cellular mechanisms in endocrinology, including: gene regulation, cell biology, signalling, mutations, transgenics, hormone-dependant cancers, nuclear receptors, and omics. Basic and pathophysiological studies at the molecule and cell level are considered, as well as human sample studies where this is the experimental model of choice. Technique studies including CRISPR or gene editing are also encouraged.
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