Suppr超能文献

醛固酮合酶的免疫组织化学为原发性醛固酮增多症的发病机制研究指明了方向。

Immunohistochemistry of aldosterone synthase leads the way to the pathogenesis of primary aldosteronism.

作者信息

Nishimoto Koshiro, Koga Minae, Seki Tsugio, Oki Kenji, Gomez-Sanchez Elise P, Gomez-Sanchez Celso E, Naruse Mitsuhide, Sakaguchi Tomokazu, Morita Shinya, Kosaka Takeo, Oya Mototsugu, Ogishima Tadashi, Yasuda Masanori, Suematsu Makoto, Kabe Yasuaki, Omura Masao, Nishikawa Tetsuo, Mukai Kuniaki

机构信息

Department of Uro-Oncology, Saitama Medical University International Medical Center, Hidaka 350-1241, Japan; Department of Biochemistry, Keio University School of Medicine, 35 Shinanomachi, Shinjuku-ku, Tokyo 160-8582, Japan.

Endocrinology & Diabetes Center, Yokohama Rosai Hospital, Yokohama 222-0036, Japan.

出版信息

Mol Cell Endocrinol. 2017 Feb 5;441:124-133. doi: 10.1016/j.mce.2016.10.014. Epub 2016 Oct 14.

Abstract

Our group previously purified human and rat aldosterone synthase (CYP11B2 and Cyp11b2, respectively) from their adrenals and verified that it is distinct from steroid 11β-hydroxylase (CYP11B1 or Cyp11b1), the cortisol- or corticosterone-synthesizing enzyme. We now describe their distributions immunohistochemically with specific antibodies. In rats, there is layered functional zonation with the Cyp11b2-positive zona glomerulosa (ZG), Cyp11b1-positive zona fasciculata (ZF), and Cyp11b2/Cyp11b1-negative undifferentiated zone between the ZG and ZF. In human infants and children (<12 years old), the functional zonation is similar to that in rats. In adults, the adrenal cortex remodels and subcapsular aldosterone-producing cell clusters (APCCs) replace the continuous ZG layer. We recently reported possible APCC-to-APA transitional lesions (pAATLs) in 2 cases of unilateral multiple adrenocortical micro-nodules. In this review, we present 4 additional cases of primary aldosteronism, from which the extracted adrenals contain pAATLs, with results of next generation sequencing for these lesions. Immunohistochemistry for CYP11B2 and CYP11B1 has become an important tool for the diagnosis of and research on adrenocortical pathological conditions and suggests that APCCs may be the origin of aldosterone-producing adenoma.

摘要

我们团队之前从人及大鼠的肾上腺中纯化出了人及大鼠醛固酮合酶(分别为CYP11B2和Cyp11b2),并证实其与皮质醇或皮质酮合成酶——类固醇11β-羟化酶(CYP11B1或Cyp11b1)不同。我们现在用特异性抗体通过免疫组织化学方法描述它们的分布情况。在大鼠中,存在分层的功能分区,球状带(ZG)Cyp11b2阳性,束状带(ZF)Cyp11b1阳性,ZG和ZF之间为Cyp11b2/Cyp11b1阴性的未分化区。在人类婴幼儿及儿童(<12岁)中,功能分区与大鼠相似。在成年人中,肾上腺皮质重塑,被膜下醛固酮分泌细胞簇(APCCs)取代了连续的ZG层。我们最近报道了2例单侧多发性肾上腺皮质微小结节中可能存在的APCC到醛固酮瘤(APA)的过渡性病变(pAATLs)。在这篇综述中,我们展示了另外4例原发性醛固酮增多症病例,其切除的肾上腺中含有pAATLs,并给出了这些病变的二代测序结果。CYP11B2和CYP11B1的免疫组织化学已成为肾上腺皮质病理状况诊断和研究的重要工具,并提示APCCs可能是醛固酮分泌腺瘤的起源。

相似文献

1
Immunohistochemistry of aldosterone synthase leads the way to the pathogenesis of primary aldosteronism.
Mol Cell Endocrinol. 2017 Feb 5;441:124-133. doi: 10.1016/j.mce.2016.10.014. Epub 2016 Oct 14.
2
Case Report: Nodule Development From Subcapsular Aldosterone-Producing Cell Clusters Causes Hyperaldosteronism.
J Clin Endocrinol Metab. 2016 Jan;101(1):6-9. doi: 10.1210/jc.2015-3285. Epub 2015 Nov 18.
3
Adrenal cortex remodeling and functional zona glomerulosa hyperplasia in primary aldosteronism.
Hypertension. 2010 Nov;56(5):885-92. doi: 10.1161/HYPERTENSIONAHA.110.158543. Epub 2010 Oct 11.
4
Human Adrenocortical Remodeling Leading to Aldosterone-Producing Cell Cluster Generation.
Int J Endocrinol. 2016;2016:7834356. doi: 10.1155/2016/7834356. Epub 2016 Sep 18.
5
Characterization of Aldosterone-producing Cell Cluster (APCC) at Single-cell Resolution.
J Clin Endocrinol Metab. 2022 Aug 18;107(9):2439-2448. doi: 10.1210/clinem/dgac394.
7
Histopathological diagnosis of primary aldosteronism using CYP11B2 immunohistochemistry.
J Clin Endocrinol Metab. 2013 Apr;98(4):1567-74. doi: 10.1210/jc.2012-3726. Epub 2013 Feb 26.
8
Pathology and gene mutations of aldosterone-producing lesions.
Endocr J. 2023 Dec 28;70(12):1113-1122. doi: 10.1507/endocrj.EJ22-0492. Epub 2023 Sep 26.
9
Aldosterone-stimulating somatic gene mutations are common in normal adrenal glands.
Proc Natl Acad Sci U S A. 2015 Aug 18;112(33):E4591-9. doi: 10.1073/pnas.1505529112. Epub 2015 Aug 3.

引用本文的文献

2
Aldosterone-producing Multiple Micronodules With Several Different Pathogenic Variants.
JCEM Case Rep. 2024 Nov 20;2(12):luae213. doi: 10.1210/jcemcr/luae213. eCollection 2024 Dec.
3
Glucocorticoids with or without fludrocortisone in septic shock: a narrative review from a biochemical and molecular perspective.
Br J Anaesth. 2024 Jan;132(1):53-65. doi: 10.1016/j.bja.2023.10.034. Epub 2023 Nov 28.
4
Primary aldosteronism: Pathophysiological mechanisms of cell death and proliferation.
Front Endocrinol (Lausanne). 2022 Aug 8;13:934326. doi: 10.3389/fendo.2022.934326. eCollection 2022.
5
Pathogenesis of Primary Aldosteronism: Impact on Clinical Outcome.
Front Endocrinol (Lausanne). 2022 Jun 23;13:927669. doi: 10.3389/fendo.2022.927669. eCollection 2022.
6
CIRMI-a new term for a concept worthy of further exploration: a narrative review.
Ann Transl Med. 2022 Jun;10(11):646. doi: 10.21037/atm-21-5572.
7
Characterization of Aldosterone-producing Cell Cluster (APCC) at Single-cell Resolution.
J Clin Endocrinol Metab. 2022 Aug 18;107(9):2439-2448. doi: 10.1210/clinem/dgac394.
8
Primary Aldosteronism: State-of-the-Art Review.
Am J Hypertens. 2022 Dec 8;35(12):967-988. doi: 10.1093/ajh/hpac079.
9
Mutant in Aldosterone-Producing Adenoma Leads to Cell Proliferation.
Int J Mol Sci. 2021 Oct 12;22(20):10981. doi: 10.3390/ijms222010981.
10
Development of [F]AldoView as the First Highly Selective Aldosterone Synthase PET Tracer for Imaging of Primary Hyperaldosteronism.
J Med Chem. 2021 Jul 8;64(13):9321-9329. doi: 10.1021/acs.jmedchem.1c00539. Epub 2021 Jun 17.

本文引用的文献

1
Human Adrenocortical Remodeling Leading to Aldosterone-Producing Cell Cluster Generation.
Int J Endocrinol. 2016;2016:7834356. doi: 10.1155/2016/7834356. Epub 2016 Sep 18.
2
Somatic KCNJ5 mutation occurring early in adrenal development may cause a novel form of juvenile primary aldosteronism.
Mol Cell Endocrinol. 2017 Feb 5;441:134-139. doi: 10.1016/j.mce.2016.07.031. Epub 2016 Aug 8.
3
Disorganized Steroidogenesis in Adrenocortical Carcinoma, a Case Study.
Endocr Pathol. 2017 Mar;28(1):27-35. doi: 10.1007/s12022-016-9441-8.
4
Case Report: Nodule Development From Subcapsular Aldosterone-Producing Cell Clusters Causes Hyperaldosteronism.
J Clin Endocrinol Metab. 2016 Jan;101(1):6-9. doi: 10.1210/jc.2015-3285. Epub 2015 Nov 18.
5
Aldosterone-stimulating somatic gene mutations are common in normal adrenal glands.
Proc Natl Acad Sci U S A. 2015 Aug 18;112(33):E4591-9. doi: 10.1073/pnas.1505529112. Epub 2015 Aug 3.
6
Adrenal nodularity and somatic mutations in primary aldosteronism: one node is the culprit?
J Clin Endocrinol Metab. 2014 Jul;99(7):E1341-51. doi: 10.1210/jc.2013-4255. Epub 2014 Apr 23.
7
Sodium deficiency regulates rat adrenal zona glomerulosa gene expression.
Endocrinology. 2014 Apr;155(4):1363-72. doi: 10.1210/en.2013-1999. Epub 2014 Jan 14.
8
Development of monoclonal antibodies against human CYP11B1 and CYP11B2.
Mol Cell Endocrinol. 2014 Mar 5;383(1-2):111-7. doi: 10.1016/j.mce.2013.11.022. Epub 2013 Dec 8.
9
Somatic mutations in ATP1A1 and CACNA1D underlie a common subtype of adrenal hypertension.
Nat Genet. 2013 Sep;45(9):1055-60. doi: 10.1038/ng.2716. Epub 2013 Aug 4.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验