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胰岛素降解酶对胰岛素敏感性的调节作用

Modulation of Insulin Sensitivity by Insulin-Degrading Enzyme.

作者信息

González-Casimiro Carlos M, Merino Beatriz, Casanueva-Álvarez Elena, Postigo-Casado Tamara, Cámara-Torres Patricia, Fernández-Díaz Cristina M, Leissring Malcolm A, Cózar-Castellano Irene, Perdomo Germán

机构信息

Instituto de Biología y Genética Molecular, University of Valladolid-CSIC, 47003 Valladolid, Spain.

Molecular Oncology Group, IMDEA Food Institute, CEI UAM + CSIC, 28049 Madrid, Spain.

出版信息

Biomedicines. 2021 Jan 17;9(1):86. doi: 10.3390/biomedicines9010086.

DOI:10.3390/biomedicines9010086
PMID:33477364
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7830943/
Abstract

Insulin-degrading enzyme (IDE) is a highly conserved and ubiquitously expressed metalloprotease that degrades insulin and several other intermediate-size peptides. For many decades, IDE had been assumed to be involved primarily in hepatic insulin clearance, a key process that regulates availability of circulating insulin levels for peripheral tissues. Emerging evidence, however, suggests that IDE has several other important physiological functions relevant to glucose and insulin homeostasis, including the regulation of insulin secretion from pancreatic β-cells. Investigation of mice with tissue-specific genetic deletion of in the liver and pancreatic β-cells (L-IDE-KO and B-IDE-KO mice, respectively) has revealed additional roles for IDE in the regulation of hepatic insulin action and sensitivity. In this review, we discuss current knowledge about IDE's function as a regulator of insulin secretion and hepatic insulin sensitivity, both evaluating the classical view of IDE as an insulin protease and also exploring evidence for several non-proteolytic functions. Insulin proteostasis and insulin sensitivity have both been highlighted as targets controlling blood sugar levels in type 2 diabetes, so a clearer understanding the physiological functions of IDE in pancreas and liver could led to the development of novel therapeutics for the treatment of this disease.

摘要

胰岛素降解酶(IDE)是一种高度保守且广泛表达的金属蛋白酶,可降解胰岛素及其他几种中等大小的肽。几十年来,人们一直认为IDE主要参与肝脏胰岛素清除,这是调节外周组织循环胰岛素水平可用性的关键过程。然而,新出现的证据表明,IDE具有其他一些与葡萄糖和胰岛素稳态相关的重要生理功能,包括调节胰腺β细胞的胰岛素分泌。对肝脏和胰腺β细胞中组织特异性基因缺失的小鼠(分别为L-IDE-KO和B-IDE-KO小鼠)的研究揭示了IDE在调节肝脏胰岛素作用和敏感性方面的其他作用。在这篇综述中,我们讨论了关于IDE作为胰岛素分泌和肝脏胰岛素敏感性调节剂的当前知识,既评估了IDE作为胰岛素蛋白酶的传统观点,也探讨了其几种非蛋白水解功能的证据。胰岛素蛋白稳态和胰岛素敏感性均被强调为控制2型糖尿病血糖水平的靶点,因此更清楚地了解IDE在胰腺和肝脏中的生理功能可能会导致开发出治疗该疾病的新型疗法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc63/7830943/e7c928fabc0c/biomedicines-09-00086-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc63/7830943/a8da00836286/biomedicines-09-00086-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc63/7830943/237af75db3f6/biomedicines-09-00086-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc63/7830943/e7c928fabc0c/biomedicines-09-00086-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc63/7830943/a8da00836286/biomedicines-09-00086-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc63/7830943/237af75db3f6/biomedicines-09-00086-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bc63/7830943/e7c928fabc0c/biomedicines-09-00086-g003.jpg

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Mol Cell. 2020 Oct 15;80(2):183-192. doi: 10.1016/j.molcel.2020.08.020. Epub 2020 Sep 17.
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Hepatic insulin-degrading enzyme regulates glucose and insulin homeostasis in diet-induced obese mice.肝胰岛素降解酶调节饮食诱导肥胖小鼠的葡萄糖和胰岛素稳态。
揭示ATP结合盒(ABC)转运蛋白在胰岛素抵抗诱导的淀粉样蛋白生成中的新机制。
Metab Brain Dis. 2025 Jun 7;40(5):218. doi: 10.1007/s11011-025-01642-6.
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Decreased expression of insulin-degrading enzyme increases gluconeogenesis and glucose production in cultured hepatocytes administered with glucagon.胰岛素降解酶表达降低会增加给予胰高血糖素的培养肝细胞中的糖异生作用和葡萄糖生成。
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