Cargando…

The cytosolic exonuclease TREX1 inhibits the innate immune response to HIV-1

Viral infection triggers innate immune sensors to produce type I interferons (IFN). However, HIV infection of T cells and macrophages does not trip these alarms. How HIV avoids activating nucleic acid sensors is unknown. The cytosolic exonuclease TREX1 suppressed IFN triggered by HIV. In Trex1(−/−)...

Descripción completa

Detalles Bibliográficos
Autores principales: Yan, Nan, Regalado-Magdos, Ashton D., Stiggelbout, Bart, Lee-Kirsch, Min Ae, Lieberman, Judy
Formato: Texto
Lenguaje:English
Publicado: 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2958248/
https://www.ncbi.nlm.nih.gov/pubmed/20871604
http://dx.doi.org/10.1038/ni.1941
Descripción
Sumario:Viral infection triggers innate immune sensors to produce type I interferons (IFN). However, HIV infection of T cells and macrophages does not trip these alarms. How HIV avoids activating nucleic acid sensors is unknown. The cytosolic exonuclease TREX1 suppressed IFN triggered by HIV. In Trex1(−/−) mouse cells and human CD4(+) T cells and macrophages in which TREX1 was inhibited by RNA interference, cytosolic HIV DNA accumulated, and HIV infection induced type I IFN that inhibited HIV replication and spreading. TREX1 bound to cytosolic HIV DNA and digested excess HIV DNA that would otherwise activate IFN expression via a TBK1, STING and IRF3 dependent pathway. HIV-stimulated IFN production in cells deficient in TREX1 did not involve known nucleic acid sensors.