Author: McWhirter, Sarah M.; Barbalat, Roman; Monroe, Kathryn M.; Fontana, Mary F.; Hyodo, Mamoru; Joncker, Nathalie T.; Ishii, Ken J.; Akira, Shizuo; Colonna, Marco; Chen, Zhijian J.; Fitzgerald, Katherine A.; Hayakawa, Yoshihiro; Vance, Russell E.
Title: A host type I interferon response is induced by cytosolic sensing of the bacterial second messenger cyclic-di-GMP Document date: 2009_8_31
ID: 3b8b8p61_26
Snippet: Cell type-specific responses to cytosolic DNA and c-di-GMP Collectively, these results suggest that there are strong similarities in the signaling pathways triggered by the cytosolic presence of c-di-GMP and other nucleic acids, such as DNA and RNA. However, c-di-GMP is not structurally similar to these nucleic acid ligands. The DNA molecules capable of provoking cytosolic responses are double stranded and >25 deoxyribonucleotides in length Stets.....
Document: Cell type-specific responses to cytosolic DNA and c-di-GMP Collectively, these results suggest that there are strong similarities in the signaling pathways triggered by the cytosolic presence of c-di-GMP and other nucleic acids, such as DNA and RNA. However, c-di-GMP is not structurally similar to these nucleic acid ligands. The DNA molecules capable of provoking cytosolic responses are double stranded and >25 deoxyribonucleotides in length Stetson and Medzhitov, 2006a) . In contrast, c-di-GMP is composed of two guanosine ribonucleotides (not deoxyribonucleotides) in an unusual cyclic conformation. c-di-GMP also lacks features consistent with recognition by RIG-I or Mda5, such as 5triphosphate, polyuridine, or double strandedness . Therefore, we considered whether distinct sensors might be responsible for triggering responses to DNA/RNA and c-di-GMP, and if so, whether the responses could be distinguished in certain cell types. macrophage cell line stably transfected with an NF-î«B luciferase reporter. We observed activation of the NF-î«B luciferase reporter by transfected c-di-GMP (Fig. 3 C) . Both the gel shift and reporter assays showed that the activation of NF-î«B by transfected c-di-GMP was not as strong as observed with transfected pdA:dT and pI:C. The subtle difference in NF-î«B induction between cytosolic DNA and c-di-GMP may suggest that there are distinct signaling components upstream of NF-î«B in the two pathways. Nonetheless, we concluded that transfected c-di-GMP is capable of activating NF-î«B. The relatively low levels and late time course of NF-î«B induction by c-di-GMP (as compared with induction by LPS), as well as the fact that we transfected c-di-GMP into cells, may explain why NF-î«B induction was not previously observed in response to c-di-GMP (Karaolis et al., 2007a) .
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