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