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尼尔森综合征中促肾上腺皮质激素/β-促脂素的生物合成、加工及释放

Corticotropin/beta-lipotropin biosynthesis, processing, and release in Nelson's syndrome.

作者信息

Allen R, Orwoll E, Kammer H, Kendall J

出版信息

J Clin Endocrinol Metab. 1981 Oct;53(4):887-9. doi: 10.1210/jcem-53-4-887.

Abstract

Biosynthesis and processing of ACTH/beta-lipotropin was studied in Nelson's syndrome pituitary tumor tissue grown in monolayer culture. Radiolabeled peptides were immunoprecipitated and fractionated by sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS/PAGE). Important findings include: 1) a virtual absence of 13K ACTH or 3.5K beta-endorphin production; 2) evidence indicating the presence of a 24-26K ACTH and beta-LPH containing intermediate (which implies a different order of processing from that reported in the mouse); 3) An extremely rapid rate of turnover and release of ACTH and beta-lipotropin (beta-LPH) similar to that of the mouse AtT20/D16v pituitary tumors. The latter finding is consistent with an intrinsic pituitary cell defect in the pathogenesis of this disorder.

摘要

在单层培养的尼尔森综合征垂体肿瘤组织中研究了促肾上腺皮质激素/β-促脂素的生物合成和加工过程。放射性标记的肽通过免疫沉淀法进行分离,并通过十二烷基硫酸钠-聚丙烯酰胺凝胶电泳(SDS/PAGE)进行分级分离。重要发现包括:1)几乎不产生13K促肾上腺皮质激素或3.5Kβ-内啡肽;2)有证据表明存在一种含有24-26K促肾上腺皮质激素和β-促脂素的中间体(这意味着加工顺序与小鼠中报道的不同);3)促肾上腺皮质激素和β-促脂素(β-LPH)的周转和释放速度极快,类似于小鼠AtT20/D16v垂体肿瘤。后一发现与该疾病发病机制中存在内在垂体细胞缺陷一致。

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