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胰岛素降解:机制、产物及意义。

Insulin degradation: mechanisms, products, and significance.

作者信息

Duckworth W C

机构信息

Veterans Administration Medical Center, Omaha, Nebraska.

出版信息

Endocr Rev. 1988 Aug;9(3):319-45. doi: 10.1210/edrv-9-3-319.

Abstract

Although much remains to be learned, our understanding of the mechanisms and processes by which insulin is degraded has advanced considerably over the past few years. The roles of receptor binding and internalization in mediating insulin degradation have been clarified, and the endosomal pathway for intracellular insulin degradation has been established and partially characterized. The importance of IP (IDE) in cellular insulin degradation has been established and the importance of lysosomal degradation questioned. Studies on IP have identified the degradation products resulting from insulin metabolism by this enzyme and shown that the degradation products by IP are identical with those produced by isolated hepatocytes. A major remaining question for future investigation is the potential role of insulin degradation and intracellular processing in insulin action.

摘要

尽管仍有许多有待了解之处,但在过去几年里,我们对胰岛素降解的机制和过程的理解有了很大进展。受体结合和内化在介导胰岛素降解中的作用已得到阐明,细胞内胰岛素降解的内体途径已被确立并部分得到表征。胰岛素酶(IDE)在细胞胰岛素降解中的重要性已得到确立,而溶酶体降解的重要性受到质疑。对胰岛素酶的研究已确定了该酶代谢胰岛素产生的降解产物,并表明胰岛素酶产生的降解产物与分离的肝细胞产生的降解产物相同。未来研究的一个主要遗留问题是胰岛素降解和细胞内加工在胰岛素作用中的潜在作用。

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