LY294002 attenuates inflammatory response in endotoxin-induced uveitis by downregulating JAK3 and inactivating the PI3K/Akt signaling

促炎细胞因子 PI3K/AKT/mTOR通路 蛋白激酶B 炎症 LY294002型 葡萄膜炎 睫状体 化学 医学 病理 生物 内科学 免疫学 信号转导 细胞生物学
作者
Xinyang Wu,Lijun Pu,Wei Chen,Qi Zhao,Geping Wu,Di Li,Hongyan Zhu
出处
期刊:Immunopharmacology and Immunotoxicology [Taylor & Francis]
卷期号:44 (4): 510-518 被引量:14
标识
DOI:10.1080/08923973.2022.2055565
摘要

Uveitis is a prevalent inflammatory eye disease that damages the vision of patients and even leads to blindness. LY294002, an inhibitor of PI3K, was reported to suppress the inflammation and alleviate the progression of many diseases. However, the function of LY294002 in uveitis is unclear.This study aimed to explore the function of LY294002 in endotoxin-induced uveitis (EIU).EIU rat models were established via a single intravitreal injection of LPS. At 24 h after LPS injection, the rats received LY294002 treatment for 14 days. The histopathology was observed by H&E staining. The concentration of proinflammatory cytokines in aqueous humor was tested by ELISA. The expression of proinflammatory cytokines in the iris ciliary body (ICB) and retina of EIU rats were detected by RT-qPCR. JAK3, PI3K, and Akt expression were assessed by RT-qPCR and western blotting. Translocation of Akt in rat retinal Müller cells (rMC-1) was evaluated by immunofluorescence staining.LY294002 alleviated ocular inflammation and decreased inflammatory cell infiltration in the anterior chamber, iris, ciliary body, vitreous cavity, and retina of EIU rats. LY294002 decreased the concentration of proinflammatory cytokines INF-γ, IL-17, IL-6, TNF-α, and IL-1β in aqueous humor and their expression in the ICB and retina of EIU rats. LY294002 downregulated JAK3 expression in EIU rats. LY294002 inhibited p-PI3K and p-Akt expression in EIU rats and restrained Akt translocation from cytoplasm to cell membrane in LPS-treated rMC-1 cells.LY294002 ameliorates inflammation in EIU by downregulating JAK3 and inactivating the PI3K/Akt signaling.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
英姑应助不安的怀梦采纳,获得10
1秒前
1秒前
西木完成签到,获得积分10
1秒前
EarendilK完成签到,获得积分10
1秒前
sunsun完成签到,获得积分10
1秒前
maomao发布了新的文献求助10
2秒前
XNM发布了新的文献求助10
2秒前
门前大桥下完成签到,获得积分10
2秒前
valley完成签到,获得积分10
2秒前
dududu完成签到,获得积分20
2秒前
2531020323发布了新的文献求助10
2秒前
直率的飞雪完成签到,获得积分10
3秒前
Zhou完成签到,获得积分20
3秒前
鳗鱼不尤完成签到,获得积分0
3秒前
阔达白卉完成签到,获得积分10
3秒前
AYing完成签到,获得积分10
3秒前
崔建完成签到,获得积分20
3秒前
崔崔完成签到,获得积分10
4秒前
落后妍完成签到 ,获得积分20
4秒前
大可完成签到,获得积分10
5秒前
5秒前
maye完成签到,获得积分10
5秒前
无花果应助京阿尼采纳,获得10
5秒前
十五完成签到,获得积分10
5秒前
ye完成签到,获得积分10
6秒前
lalala完成签到,获得积分10
6秒前
linlin发布了新的文献求助20
6秒前
6秒前
所所应助bobo采纳,获得10
7秒前
生动初蓝完成签到,获得积分10
7秒前
LRY完成签到,获得积分10
7秒前
ZYY完成签到,获得积分10
7秒前
17777777完成签到 ,获得积分10
7秒前
Ethan发布了新的文献求助10
7秒前
dududu发布了新的文献求助20
7秒前
molihuakai应助动人的以蓝采纳,获得10
8秒前
cdercder应助luilui采纳,获得10
8秒前
wlz完成签到,获得积分10
9秒前
Netsky发布了新的文献求助10
9秒前
赘婿应助林途采纳,获得10
9秒前
高分求助中
Principles of Economics, 11th Edition 10000
University Physics with Modern Physics, 16th edition 10000
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
Arthritis and Related Conditions, An Issue of Orthopedic Clinics 1000
Development of a Bridge Weigh-In-Motion System: A technology to convert the bridge response to the passage of traffic into data on vehicle configurations, speeds, times of travel and weights 1000
ズームレンズの光学設計に関する研究 800
Fundamentals of Pharmaceutical and Biologics Regulations: A Global Perspective, Second Edition 700
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 工程类 有机化学 化学工程 生物化学 计算机科学 内科学 物理 复合材料 催化作用 细胞生物学 无机化学 光电子学 物理化学 电极 基因
热门帖子
关注 科研通微信公众号,转发送积分 7291451
求助须知:如何正确求助?哪些是违规求助? 8910443
关于积分的说明 18860692
捐赠科研通 6958809
什么是DOI,文献DOI怎么找? 3209327
关于科研通互助平台的介绍 2378998
邀请新用户注册赠送积分活动 2185172