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LAT通过LAT-磷脂酶C-γ1相互作用减轻卵清蛋白诱导的过敏性哮喘小鼠模型中的Th2/Treg失衡。

LAT alleviates Th2/Treg imbalance in an OVA-induced allergic asthma mouse model through LAT-PLC-γ1 interaction.

作者信息

Chen Xi, Li Xiao-Ming, Gu Wen, Wang Di, Chen Yi, Guo Xue-Jun

机构信息

Department of Respirology Medicine, Xinhua Hospital, School of Medicine, Shanghai Jiaotong University, Shanghai 200092, China.

Department of Respirology Medicine, Xinhua Hospital, School of Medicine, Shanghai Jiaotong University, Shanghai 200092, China.

出版信息

Int Immunopharmacol. 2017 Mar;44:9-15. doi: 10.1016/j.intimp.2016.12.029. Epub 2017 Jan 4.

Abstract

INTRODUCTION

Low expression of linker for activation of T cells (LAT) is observed in asthma. LAT and its downstream regulator, phospholipase C-gamma 1 (PLC-γ1) play important roles in the T cell antigen receptor signaling pathway, and their interaction is associated with CD4 cell polarization. Here, we investigated whether LAT can alleviate the imbalance among CD4 cell subgroups and the possible mechanism.

METHODS

An ovalbumin-induced allergic asthma mouse model was established and LAT plasmid was delivered. The pathological changes in lung were evaluated by hematoxylin and eosin and periodic acid-Schiff staining. The typical cytokines released by T helper 2 (Th2) and regulatory T (Treg) cells were measured using enzyme-linked immunosorbent assay and the number of Th1, Th2, and Treg cells were determined using flow cytometry. Lung CD4 T cells were isolated by magnetic isolation. The mRNA expression of LAT and PLC-γ1 was determined by real-time PCR. Co-Immunoprecipitation was performed to confirm the interaction between LAT and PLC-γ1. The protein expression of LAT, PLC-γ1 and corresponding downstream signaling factors were determined by western blotting.

RESULTS

The delivery of LAT DNA to the lung could suppress an overactive Th2 response by decreasing allergic response and Th2 cytokine secretion, and by increasing Treg cytokine secretion. The Th2/Treg imbalance in lung and decreased phosphorylated PLC-γ1 expression in lung CD4 T cells were rectified by LAT DNA delivery. Excessive activation of the Raf-MEK-ERK and PI3K-AKT-CREB pathways after asthma is attenuated by LAT.

CONCLUSION

The site-specific delivery of LAT DNA to the lung could suppress an overactive Th2 response and rectify the Th2/Treg imbalance in asthmatic mouse model. LAT-PLC-γ1 interaction may contribute to LAT activity in vivo and LAT protects against asthma partly via Raf-MEK-ERK and PI3K-AKT-CREB pathways. The delivery of LAT DNA could offer a novel and safe strategy for asthma prevention.

摘要

引言

在哮喘中观察到T细胞活化连接蛋白(LAT)表达降低。LAT及其下游调节因子磷脂酶C-γ1(PLC-γ1)在T细胞抗原受体信号通路中起重要作用,它们的相互作用与CD4细胞极化相关。在此,我们研究了LAT是否能缓解CD4细胞亚群之间的失衡及其可能的机制。

方法

建立卵清蛋白诱导的过敏性哮喘小鼠模型并递送LAT质粒。通过苏木精-伊红染色和高碘酸-希夫染色评估肺部的病理变化。使用酶联免疫吸附测定法测量辅助性T细胞2(Th2)和调节性T(Treg)细胞释放的典型细胞因子,并使用流式细胞术确定Th1、Th2和Treg细胞的数量。通过磁珠分离法分离肺CD4 T细胞。通过实时PCR测定LAT和PLC-γ1的mRNA表达。进行免疫共沉淀以确认LAT与PLC-γ1之间的相互作用。通过蛋白质印迹法测定LAT、PLC-γ1及相应下游信号因子的蛋白表达。

结果

将LAT DNA递送至肺部可通过降低过敏反应和Th2细胞因子分泌以及增加Treg细胞因子分泌来抑制过度活跃的Th2反应。LAT DNA递送纠正了肺部的Th2/Treg失衡以及肺CD4 T细胞中磷酸化PLC-γ1表达的降低。哮喘后Raf-MEK-ERK和PI3K-AKT-CREB途径的过度激活被LAT减弱。

结论

将LAT DNA位点特异性递送至肺部可抑制过度活跃的Th2反应并纠正哮喘小鼠模型中的Th2/Treg失衡。LAT-PLC-γ1相互作用可能有助于LAT在体内的活性,并且LAT部分通过Raf-MEK-ERK和PI3K-AKT-CREB途径预防哮喘。LAT DNA的递送可为哮喘预防提供一种新的安全策略。

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