| Literature DB >> 26046437 |
Janna Seifried1, Stephen Soonthornvacharin2, Sunnie M Yoh2, Monika Schneider2, Rana E Akleh2, Kevin C Olivieri2, Paul D De Jesus2, Chunhai Ruan3, Elisa de Castro4, Pedro A Ruiz2, David Germanaud5, Vincent des Portes6, Adolfo García-Sastre4,7, Renate König1,2,8, Sumit K Chanda2.
Abstract
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.Entities:
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Year: 2015 PMID: 26046437 PMCID: PMC4503237 DOI: 10.1016/j.cell.2015.04.050
Source DB: PubMed Journal: Cell ISSN: 0092-8674 Impact factor: 41.582