STING recognition of cytoplasmic DNA instigates cellular defense.
Mol Cell, 2013/4/11;50(1):5-15.
Abe T[1], Harashima A, Xia T, Konno H, Konno K, Morales A, Ahn J, Gutman D, Barber GN
Affiliations
PMID: 23478444
Impact factor: 19.328
Abstract
How the cell recognizes cytosolic DNA including DNA-based microbes to trigger host-defense-related gene activation remains to be fully resolved. Here, we demonstrate that STING (stimulator of interferon genes), an endoplasmic reticulum translocon-associated transmembrane protein, acts to detect cytoplasmic DNA species. STING homodimers were able to complex with self- (apoptotic, necrotic) or pathogen-related ssDNA and dsDNA and were indispensible for HSV-1-mediated transcriptional activation of a wide array of innate immune and proinflammatory genes in addition to type I IFN. Our data indicate that STING instigates cytoplasmic DNA-mediated cellular defense gene transcription and facilitates adoptive responses that are required for protection of the host. In contrast, chronic STING activation may manifest inflammatory responses and possibly autoimmune disease triggered by self-DNA.
MeSH terms
Animals; Apoptosis; Binding Sites; Cytoplasm; DNA, Single-Stranded; Genes, Reporter; HEK293 Cells; Herpesvirus 1, Human; Humans; Immunity, Innate; Inflammation Mediators; Interferon Type I; Luciferases, Firefly; Membrane Proteins; Mice; Necrosis; Protein Multimerization; RNA Interference; Telomerase; Transcription, Genetic; Transfection
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