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肽酰精氨酸脱亚氨酶在小鼠唾液腺中的激活导致 Ro 和 La 核糖核蛋白的瓜氨酸化。

Activation of Peptidylarginine Deiminase in the Salivary Glands of Mice Drives the Citrullination of Ro and La Ribonucleoproteins.

机构信息

Department of Immunology, Unidad Académica de Ciencias Biológicas, Universidad Autónoma de Zacatecas, Guadalupe, ZAC, Mexico.

Pharmacology PhD Program, Centro Universitario de Ciencias de la Salud (CUCS), Universidad de Guadalajara, Guadalajara, JAL, Mexico.

出版信息

J Immunol Res. 2017;2017:8959687. doi: 10.1155/2017/8959687. Epub 2017 Nov 26.

Abstract

The goal of the present study was to determine whether peptidylarginine deiminase PAD2 and PAD4 enzymes are present in mouse salivary glands and whether they are able to citrullinate Ro and La ribonucleoproteins. Salivary glands from mice were cultured in DMEM and supplemented with one of the following stimulants: ATP, LPS, TNF, IFN, or IL-6. A control group without stimulant was also evaluated. PAD2, PAD4, citrullinated peptides, Ro60, and La were detected by immunohistochemistry and double immunofluorescence. PAD2 and PAD4 mRNAs and protein expression were detected by qPCR and Western blot analysis. PAD activity was assessed using an antigen capture enzyme-linked immunosorbent assay. LPS, ATP, and TNF triggered PAD2 and PAD4 expression; in contrast, no expression was detected in the control group ( < 0.001). PAD transcription slightly increased in response to stimulation. Additionally, PAD2/4 activity modified the arginine residues of a reporter protein (fibrinogen) . PADs citrullinated Ro60 and La ribonucleoproteins . Molecular stimulants induced apoptosis in ductal cells and the externalization of Ro60 and La ribonucleoproteins onto apoptotic membranes. PAD enzymes citrullinate Ro and La ribonucleoproteins, and this experimental approach may facilitate our understanding of the role of posttranslational modifications in the pathophysiology of Sjögren's syndrome.

摘要

本研究旨在确定肽基精氨酸脱亚氨酶 PAD2 和 PAD4 酶是否存在于小鼠唾液腺中,以及它们是否能够使 Ro 和 La 核糖核蛋白发生瓜氨酸化。将来自 C57BL/6 小鼠的唾液腺在 DMEM 中培养,并添加以下刺激物之一:ATP、LPS、TNF、IFN 或 IL-6。还评估了没有刺激物的对照组。通过免疫组织化学和双重免疫荧光检测 PAD2、PAD4、瓜氨酸化肽、Ro60 和 La。通过 qPCR 和 Western blot 分析检测 PAD2 和 PAD4 mRNA 和蛋白表达。使用抗原捕获酶联免疫吸附试验评估 PAD 活性。LPS、ATP 和 TNF 触发 PAD2 和 PAD4 表达;相比之下,对照组未检测到表达(<0.001)。刺激后 PAD 转录略有增加。此外,PAD2/4 活性修饰了报告蛋白(纤维蛋白原)的精氨酸残基。PADs 使 Ro60 和 La 核糖核蛋白瓜氨酸化。分子刺激物诱导导管细胞凋亡,并使 Ro60 和 La 核糖核蛋白外排在凋亡膜上。PAD 酶使 Ro 和 La 核糖核蛋白瓜氨酸化,这种实验方法可能有助于我们理解翻译后修饰在干燥综合征病理生理学中的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/81ee/5727760/fcd6bd6804e6/JIR2017-8959687.001.jpg

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