ABCC3是人肾上腺皮质cyp11b2阴性肾小球带细胞的差异标志物。

IF 11.3 2区 医学 Q1 ENDOCRINOLOGY & METABOLISM
Yingxian Pang, Sanas Mir-Bashiri, Zhuolun Sun, Yuhong Yang, Isabella Castellano, Thomas Knösel, Martin Reincke, Tracy Ann Williams
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引用次数: 0

摘要

ATP结合盒亚家族C成员3 (ABCC3)是一种输出多种化合物的膜转运蛋白,影响癌症的耐药性,并影响代谢和恶性疾病。我们之前报道了在脂质过氧化诱导的氧化应激下,ABCC3在人肾上腺细胞中的上调。在原发性醛固酮增多症的背景下,我们研究了ABCC3在人肾上腺皮质中的表达和功能,重点研究了它与肾小球带(ZG)细胞中CYP11B2(醛固酮合成酶)和醛固酮产生病变的关系。ABCC3在醛固酮产生性腺瘤(APAs)中的表达与邻近肾上腺皮质、皮质醇产生性腺瘤和无功能性腺瘤相比明显降低。APAs的减少显示出基因型变异性:在携带KCNJ5突变的APAs中,abcc3 mRNA/蛋白水平显著高于野生型KCNJ5 APAs。KCNJ5突变是通过改变钾通道功能自主产生醛固酮的已知驱动因素。空间转录组学和免疫荧光共定位显示ABCC3和CYP11B2(醛固酮合成酶)在APAs和醛固酮生成微模块(APMs)中呈负表达模式。值得注意的是,ABCC3的高表达仅在缺乏CYP11B2表达的肾上腺ZG细胞中观察到。这种表达模式将ABCC3与常见的ZG标记物(如KCNJ5和DAB2)区分开来,后者在肾上腺ZG细胞、APMs和APA肿瘤细胞中表达。在培养的人肾上腺皮质细胞中,血管紧张素II刺激和诱导KCNJ5-L168R突变的表达都会导致CYP11B2转录上调,同时抑制ABCC3的表达。总之,ABCC3作为cyp11b2阴性ZG细胞的新标记物,提供了一种组织病理学工具,用于区分原发性醛固酮增多症中正常肾上腺带化与醛固酮产生病变,以及与皮质醇产生和无功能腺瘤。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
ABCC3 Is a Differential Marker of CYP11B2-Negative Zona Glomerulosa Cells in Human Adrenal Cortex.

ATP Binding Cassette Subfamily C Member 3 (ABCC3) is a membrane transporter that exports diverse compounds, influencing drug resistance in cancers and impacting metabolic and malignant diseases. We previously reported ABCC3 upregulation in human adrenal cells under lipid peroxidation-induced oxidative stress. We investigated ABCC3 expression and function in the human adrenal cortex in the context of primary aldosteronism, focusing on its relationship to CYP11B2 (aldosterone synthase) in zona glomerulosa (ZG) cells and aldosterone-producing lesions. ABCC3 expression in aldosterone-producing adenomas (APAs) was markedly reduced compared to the adjacent adrenal cortex, cortisol-producing adenomas, and non-functioning adenomas. The reduction in APAs showed genotypic variability: in APAs harboring KCNJ5 mutations-known drivers of autonomous aldosterone production via altered potassium channel function-ABCC3 mRNA/protein levels were significantly higher than in wild-type KCNJ5 APAs. Spatial transcriptomics and immunofluorescence colocalization revealed an inverse expression pattern between ABCC3 and CYP11B2 (aldosterone synthase) in APAs and aldosterone-producing micronodules (APMs). Notably, high ABCC3 expression was exclusively observed in adrenal ZG cells that lacked CYP11B2 expression. This expression pattern distinguishes ABCC3 from common ZG markers such as KCNJ5 and DAB2, which are expressed across adrenal ZG cells, APMs, and APA tumor cells. In cultured human adrenocortical cells, both angiotensin II stimulation and induced expression of the KCNJ5-L168R mutation resulted in upregulation of CYP11B2 transcription while concomitantly suppressing ABCC3 expression. In conclusion, ABCC3 serves as a novel marker of CYP11B2-negative ZG cells, providing a histopathological tool to differentiate normal adrenal zonation from aldosterone-producing lesions in primary aldosteronism, as well as from cortisol-producing and nonfunctional adenomas.

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来源期刊
Endocrine Pathology
Endocrine Pathology 医学-病理学
CiteScore
12.30
自引率
20.50%
发文量
41
审稿时长
>12 weeks
期刊介绍: Endocrine Pathology publishes original articles on clinical and basic aspects of endocrine disorders. Work with animals or in vitro techniques is acceptable if it is relevant to human normal or abnormal endocrinology. Manuscripts will be considered for publication in the form of original articles, case reports, clinical case presentations, reviews, and descriptions of techniques. Submission of a paper implies that it reports unpublished work, except in abstract form, and is not being submitted simultaneously to another publication. Accepted manuscripts become the sole property of Endocrine Pathology and may not be published elsewhere without written consent from the publisher. All articles are subject to review by experienced referees. The Editors and Editorial Board judge manuscripts suitable for publication, and decisions by the Editors are final.
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