Suppr超能文献

ICTH 通过硫氧还蛋白相互作用蛋白调节高糖诱导的人晶状体上皮细胞氧化应激。

ITCH regulates oxidative stress induced by high glucose through thioredoxin interacting protein in cultured human lens epithelial cells.

机构信息

Department of Ophthalmology, Fourth Affiliated Hospital of China Medical University, Ophthalmology Hospital of China Medical University, Key Laboratory of Lens in Liaoning Province, Shenyang, Liaoning 110005, P.R. China.

出版信息

Mol Med Rep. 2020 Nov;22(5):4307-4319. doi: 10.3892/mmr.2020.11499. Epub 2020 Sep 9.

Abstract

Thioredoxin (Trx) is an important protein that controls oxidative damage in almost all eukaryotic cells. Trx interaction protein (Txnip) has been reported to negatively regulate the bioavailability of Trx and inhibit its biological function. The E3 ubiquitin ligase ITCH can specifically degrade Txnip via ubiquitination. The apoptosis of human lens epithelial cells (HLECs), which are highly sensitive to redox caused by oxidative stress, is a significant factor for the development of sugar cataract in a high‑glucose environment. However, whether Trx, Txnip and ITCH contribute to the progression of sugar cataracts and the underlying mechanisms remain unknown, and thus, identifying these were the aims of the present study. The present results suggested that the expression levels of Trx, Txnip and ITCH in HLECs cultured with different glucose concentrations were detected by reverse transcription‑quantitative PCR and western blotting, and the apoptotic rate of the cells was detected by flow cytometry and superoxide detection assay. The interaction between ITCH and Txnip was determined by co‑localization immunofluorescence and co‑immunoprecipitation. In addition, a vector and small interfering RNA of ITCH were transfected to overexpress and knockdown ITCH, respectively, to alter the expression of downstream proteins and cell apoptosis. It was found that Txnip was highly expressed in cultured HLECs in high‑glucose environment, and the antioxidative function of Trx was restricted and suppressed, thus promoting apoptosis. The overexpression of ITCH increased the expression of Trx and decreased oxidative stress and apoptosis by decreasing Txnip in cultured HLECs, while downregulation of ITCH significantly decreased the expression of Trx and enhanced oxidative stress and apoptosis. Therefore, the present results indicated that ITCH could regulate the apoptosis of HLECs that were cultured in high‑glucose concentration and that it may be a treatment target for sugar cataract.

摘要

硫氧还蛋白(Trx)是一种重要的蛋白质,几乎可以控制所有真核细胞的氧化损伤。已报道硫氧还蛋白相互作用蛋白(Txnip)可负调控 Trx 的生物利用度并抑制其生物学功能。E3 泛素连接酶 ITCH 可通过泛素化特异性降解 Txnip。人晶状体上皮细胞(HLECs)对氧化应激引起的氧化还原非常敏感,其凋亡是人在高糖环境下发生糖性白内障的一个重要因素。然而,Trx、Txnip 和 ITCH 是否有助于糖性白内障的进展及其潜在机制尚不清楚,因此,本研究旨在确定这些蛋白。本研究结果表明,通过逆转录-定量 PCR 和 Western blot 检测不同葡萄糖浓度培养的 HLECs 中 Trx、Txnip 和 ITCH 的表达水平,通过流式细胞术和超氧化物检测法检测细胞的凋亡率。通过共定位免疫荧光和共免疫沉淀检测 ITCH 和 Txnip 之间的相互作用。此外,转染 ITCH 载体和小干扰 RNA 分别过表达和敲低 ITCH,以改变下游蛋白的表达和细胞凋亡。结果发现,高糖环境培养的 HLECs 中 Txnip 高表达,Trx 的抗氧化功能受到限制和抑制,从而促进细胞凋亡。ITCH 的过表达通过降低 Txnip 增加了培养的 HLECs 中 Trx 的表达,降低了氧化应激和细胞凋亡,而下调 ITCH 则显著降低了 Trx 的表达,增强了氧化应激和细胞凋亡。因此,本研究结果表明,ITCH 可调节高糖浓度培养的 HLECs 的凋亡,它可能是治疗糖性白内障的一个靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7623/7533507/b550fe617521/MMR-22-05-4307-g00.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验