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一个法国家系中出现的糖皮质激素可抑制性醛固酮增多症和肾上腺肿瘤。

Glucocorticoid-suppressible hyperaldosteronism and adrenal tumors occurring in a single French pedigree.

作者信息

Pascoe L, Jeunemaitre X, Lebrethon M C, Curnow K M, Gomez-Sanchez C E, Gasc J M, Saez J M, Corvol P

机构信息

INSERM U36, Collège de France, Paris, France.

出版信息

J Clin Invest. 1995 Nov;96(5):2236-46. doi: 10.1172/JCI118279.

Abstract

Glucocorticoid-suppressible hyperaldosteronism is a dominantly inherited form of hypertension believed to be caused by the presence of a hybrid CYP11B1/CYP11B2 gene which has arisen from an unequal crossing over between the two CYP11B genes in a previous meiosis. We have studied a French pedigree with seven affected individuals in which two affected individuals also have adrenal tumors and two others have micronodular adrenal hyperplasia. One of the adrenal tumors and the surrounding adrenal tissue has been removed, giving a rare opportunity to study the regulation and action of the hybrid gene causing the disease. The hybrid CYP11B gene was demonstrated to be expressed at higher levels than either CYP11B1 or CYP11B2 in the cortex of the adrenal by RT-PCR and Northern blot analysis. In situ hybridization showed that both CYP11B1 and the hybrid gene were expressed in all three zones of the cortex. In cell culture experiments hybrid gene expression was stimulated by ACTH leading to increased production of aldosterone and the hybrid steroids characteristic of glucocorticoid-suppressible hyperaldosteronism. The genetic basis of the adrenal pathologies in this family is not known but may be related to the duplication causing the hyperaldosteronism.

摘要

糖皮质激素可抑制性醛固酮增多症是一种常染色体显性遗传的高血压病,据信是由一种杂交的CYP11B1/CYP11B2基因引起的,该基因源于上一次减数分裂中两个CYP11B基因之间的不等交换。我们研究了一个法国家系,其中有7名患者,其中2名患者还患有肾上腺肿瘤,另外2名患有微结节性肾上腺增生。已切除其中一个肾上腺肿瘤及其周围的肾上腺组织,这为研究导致该病的杂交基因的调控和作用提供了难得的机会。通过逆转录聚合酶链反应(RT-PCR)和Northern印迹分析表明,杂交CYP11B基因在肾上腺皮质中的表达水平高于CYP11B1或CYP11B2。原位杂交显示,CYP11B1和杂交基因在皮质的所有三个区域均有表达。在细胞培养实验中,促肾上腺皮质激素(ACTH)刺激杂交基因表达,导致醛固酮和糖皮质激素可抑制性醛固酮增多症特有的杂交类固醇生成增加。该家族肾上腺病变的遗传基础尚不清楚,但可能与导致醛固酮增多症的基因重复有关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aa74/185874/0584cf7ce7ed/jcinvest00017-0147-a.jpg

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