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pellino的细胞表面定位通过控制果蝇中MyD88的周转来拮抗Toll介导的先天免疫信号。

Cell-surface localization of Pellino antagonizes Toll-mediated innate immune signalling by controlling MyD88 turnover in Drosophila.

作者信息

Ji Shanming, Sun Ming, Zheng Xiudeng, Li Lin, Sun Liwei, Chen Dahua, Sun Qinmiao

机构信息

1] State Key Laboratory of Biomembrane and Membrane Biotechnology, Institute of Zoology, Chinese Academy of Sciences, Beijing 100101, China [2] State Key Laboratory of Reproductive Biology, Institute of Zoology, Chinese Academy of Sciences, Beijing 100101, China [3].

1] State Key Laboratory of Biomembrane and Membrane Biotechnology, Institute of Zoology, Chinese Academy of Sciences, Beijing 100101, China [2].

出版信息

Nat Commun. 2014 Mar 17;5:3458. doi: 10.1038/ncomms4458.

Abstract

Innate immunity mediated by Toll signalling has been extensively studied, but how Toll signalling is precisely controlled in balancing innate immune responses remains poorly understood. It was reported that the plasma membrane localization of Drosophila MyD88 is necessary for the recruitment of cytosolic adaptor Tube to the cell surface, thus contributing to Toll signalling transduction. Here we demonstrate that Drosophila Pellino functions as a negative regulator in Toll-mediated signalling. We show that Pellino accumulates at the plasma membrane upon the activation of Toll signalling in a MyD88-dependent manner. Moreover, we find that Pellino is associated with MyD88 via its CTE domain, which is necessary and sufficient to promote Pellino accumulation at the plasma membrane where it targets MyD88 for ubiquitination and degradation. Collectively, our study uncovers a mechanism by which a feedback regulatory loop involving MyD88 and Pellino controls Toll-mediated signalling, thereby maintaining homeostasis of host innate immunity.

摘要

由Toll信号介导的固有免疫已得到广泛研究,但Toll信号在平衡固有免疫反应中是如何被精确调控的仍知之甚少。据报道,果蝇MyD88的质膜定位对于将胞质衔接蛋白Tube招募到细胞表面是必要的,从而有助于Toll信号转导。在此我们证明,果蝇Pellino在Toll介导的信号传导中起负调节作用。我们表明,Pellino在Toll信号激活后以MyD88依赖的方式在质膜上积累。此外,我们发现Pellino通过其CTE结构域与MyD88相关联,这对于促进Pellino在质膜上的积累是必要且充分的,在质膜上它靶向MyD88进行泛素化和降解。总的来说,我们的研究揭示了一种机制,即涉及MyD88和Pellino的反馈调节环控制Toll介导的信号传导,从而维持宿主固有免疫的稳态。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d052/3959197/ce072a42182e/ncomms4458-f1.jpg

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