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神经元排斥分子Slit2抑制树突状细胞迁移及免疫反应的发生。

Neuronal repellent Slit2 inhibits dendritic cell migration and the development of immune responses.

作者信息

Guan Hongbing, Zu Guorui, Xie Yi, Tang Hao, Johnson Martin, Xu Xiaochun, Kevil Christophe, Xiong Wen-Cheng, Elmets Craig, Rao Yi, Wu Jane Y, Xu Hui

机构信息

Department of Dermatology, University of Alabama, Birmingham, AL 35294, USA.

出版信息

J Immunol. 2003 Dec 15;171(12):6519-26. doi: 10.4049/jimmunol.171.12.6519.

Abstract

One of the essential functions of dendritic cells is to take up Ags in peripheral tissues and migrate into secondary lymphoid organs to present Ags to lymphocytes for the induction of immune responses. Although many studies have demonstrated that the migration of dendritic cells is closely associated with the development of immune responses, little is known about factors that inhibit dendritic cell migration and control the extent of immune responses to Ag stimulation. We show that Slit2, a neuronal repellent factor, is up-regulated in the skin by allergen sensitization and down-regulates the migration of Langerhans cells. The effect is mediated by direct interaction of Slit2 with cells that express a Slit-specific receptor, Robo1. Slit2-mediated inhibition of Langerhans cell migration results in suppression of contact hypersensitivity responses. These findings provide insights into a novel mechanism by which Slit2 functions as an anti-inflammatory factor for the initiation of immune responses.

摘要

树突状细胞的基本功能之一是在外周组织中摄取抗原,并迁移至二级淋巴器官,将抗原呈递给淋巴细胞以诱导免疫反应。尽管许多研究表明树突状细胞的迁移与免疫反应的发展密切相关,但对于抑制树突状细胞迁移并控制对抗原刺激的免疫反应程度的因素却知之甚少。我们发现,神经元排斥因子Slit2在皮肤中因过敏原致敏而上调,并下调朗格汉斯细胞的迁移。这种效应是由Slit2与表达Slit特异性受体Robo1的细胞直接相互作用介导的。Slit2介导的朗格汉斯细胞迁移抑制导致接触性超敏反应受到抑制。这些发现为Slit2作为免疫反应起始的抗炎因子的新机制提供了见解。

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