[PDF][PDF] DDX1, DDX21, and DHX36 helicases form a complex with the adaptor molecule TRIF to sense dsRNA in dendritic cells

Z Zhang, T Kim, M Bao, V Facchinetti, SY Jung… - Immunity, 2011 - cell.com
Z Zhang, T Kim, M Bao, V Facchinetti, SY Jung, AA Ghaffari, J Qin, G Cheng, YJ Liu
Immunity, 2011cell.com
The innate immune system detects viral infection predominantly by sensing viral nucleic
acids. We report the identification of a viral sensor, consisting of RNA helicases DDX1,
DDX21, and DHX36, and the adaptor molecule TRIF, by isolation and sequencing of poly I:
C-binding proteins in myeloid dendritic cells (mDCs). Knockdown of each helicase or TRIF
by shRNA blocked the ability of mDCs to mount type I interferon (IFN) and cytokine
responses to poly I: C, influenza A virus, and reovirus. Although DDX1 bound poly I: C via its …
Summary
The innate immune system detects viral infection predominantly by sensing viral nucleic acids. We report the identification of a viral sensor, consisting of RNA helicases DDX1, DDX21, and DHX36, and the adaptor molecule TRIF, by isolation and sequencing of poly I:C-binding proteins in myeloid dendritic cells (mDCs). Knockdown of each helicase or TRIF by shRNA blocked the ability of mDCs to mount type I interferon (IFN) and cytokine responses to poly I:C, influenza A virus, and reovirus. Although DDX1 bound poly I:C via its Helicase A domain, DHX36 and DDX21 bound the TIR domain of TRIF via their HA2-DUF and PRK domains, respectively. This sensor was localized within the cytosol, independent of the endosomes. Thus, the DDX1-DDX21-DHX36 complex represents a dsRNA sensor that uses the TRIF pathway to activate type I IFN responses in the cytosol of mDCs.
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