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Src激酶抑制对仔猪动物模型脑缺氧后蛋白酪氨酸磷酸酶1B表达的影响

Effects of Src Kinase Inhibition on Expression of Protein Tyrosine Phosphatase 1B after Brain Hypoxia in a Piglet Animal Model.

作者信息

Angelis Dimitrios, Delivoria-Papadopoulos Maria

机构信息

Department of Pediatrics, Texas Tech University-HSC at the Permian Basin, Odessa, TX, USA.

Department of Pediatrics, Drexel University and St. Christopher's Hospital for Children, Philadelphia, PA, USA.

出版信息

Mediators Inflamm. 2017;2017:2810295. doi: 10.1155/2017/2810295. Epub 2017 May 23.

DOI:10.1155/2017/2810295
PMID:28626342
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5463160/
Abstract

BACKGROUND

Protein tyrosine phosphatases (PTPs) in conjunction with protein tyrosine kinases (PTKs) regulate cellular processes by posttranslational modifications of signal transduction proteins. PTP nonreceptor type 1B (PTP-1B) is an enzyme of the PTP family. We have previously shown that hypoxia induces an increase in activation of a class of nonreceptor PTK, the Src kinases. In the present study, we investigated the changes that occur in the expression of PTP-1B in the cytosolic component of the brain of newborn piglets acutely after hypoxia as well as long term for up to 2 weeks.

METHODS

Newborn piglets were divided into groups: normoxia, hypoxia, hypoxia followed by 1 day and 15 days in FiO 0.21, and hypoxia pretreated with Src kinase inhibitor PP2, prior to hypoxia followed by 1 day and 15 days. Hypoxia was achieved by providing 7% FiO for 1 hour and PTP-1B expression was measured via immunoblotting.

RESULTS

PTP-1B increased posthypoxia by about 30% and persisted for 2 weeks while Src kinase inhibition attenuated the expected PTP-1B-increased expression.

CONCLUSIONS

Our study suggests that Src kinase mediates a hypoxia-induced increased PTP-1B expression.

摘要

背景

蛋白酪氨酸磷酸酶(PTPs)与蛋白酪氨酸激酶(PTKs)共同作用,通过对信号转导蛋白进行翻译后修饰来调节细胞过程。蛋白酪氨酸磷酸酶非受体1B型(PTP - 1B)是PTP家族的一种酶。我们之前已经表明,缺氧会导致一类非受体PTK即Src激酶的激活增加。在本研究中,我们调查了新生仔猪大脑胞质成分中,急性缺氧后以及长达2周的长期缺氧后PTP - 1B表达的变化。

方法

将新生仔猪分为几组:常氧组、缺氧组、缺氧后在FiO₂ 0.21环境下饲养1天和15天的组,以及在缺氧前用Src激酶抑制剂PP2预处理,然后在缺氧后饲养1天和15天的组。通过提供7% FiO₂ 1小时来实现缺氧,并通过免疫印迹法测量PTP - 1B的表达。

结果

缺氧后PTP - 1B增加约30%,并持续2周,而Src激酶抑制减弱了预期的PTP - 1B表达增加。

结论

我们的研究表明,Src激酶介导缺氧诱导的PTP - 1B表达增加。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd77/5463160/a359f074e675/MI2017-2810295.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd77/5463160/4260a3ccee7b/MI2017-2810295.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd77/5463160/b80ac0ca9c9a/MI2017-2810295.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd77/5463160/a359f074e675/MI2017-2810295.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd77/5463160/4260a3ccee7b/MI2017-2810295.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd77/5463160/b80ac0ca9c9a/MI2017-2810295.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd77/5463160/a359f074e675/MI2017-2810295.003.jpg

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