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PQBP1 Is a Proximal Sensor of the cGAS-Dependent Innate Response to HIV-1

机译:PQBP1是cGAS依赖对HIV-1的先天反应的近端传感器。

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摘要

Dendritic cells (DCs) play a critical role in the immune response to viral infection through the facilitation of cell-intrinsic antiviral activity and the activation of adaptive immunity. HIV-1 infection of DCs triggers an IRF3-dependent innate immune response, which requires the activity of cyclic GAMP synthase (cGAS). We report the results of a targeted RNAi screen utilizing primary human monocyte-derived DCs (MDDCs) to identify immune regulators that directly interface with HIV-1-encoded features to initiate this innate response. Polyglutamine binding protein 1 (PQBP1) emerged as a strong candidate through this analysis. We found that PQBP1 directly binds to reverse-transcribed HIV-1 DNA and interacts with cGAS to initiate an IRF3-dependent innate response. MDDCs derived from Renpenning syndrome patients, who harbor mutations in the PQBP1 locus, possess a severely attenuated innate immune response to HIV-1 challenge, underscoring the role of PQBP1 as a proximal innate sensor of a HIV-1 infection.
机译:树突状细胞(DC)通过促进细胞内在的抗病毒活性和激活适应性免疫在病毒感染的免疫应答中起关键作用。 DC的HIV-1感染会触发IRF3依赖性先天免疫应答,这需要环状GAMP合酶(cGAS)的活性。我们报告了针对性的RNAi筛选的结果,该筛选利用主要的人类单核细胞衍生的DC(MDDC)来识别与HIV-1编码功能直接接口以启动此先天反应的免疫调节剂。通过此分析,聚谷氨酰胺结合蛋白1(PQBP1)成为了强有力的候选者。我们发现PQBP1直接结合到逆转录的HIV-1 DNA并与cGAS相互作用以启动IRF3依赖性先天反应。来自Renpenning综合征患者的MDDC具有PQBP1基因座的突变,其对HIV-1攻击的先天免疫应答严重减弱,强调了PQBP1作为HIV-1感染的近端先天传感器的作用。

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