@article{Xu2016443, abstract = {Summary Upon sensing cytoplasmic retroviral \{DNA\} in infected cells, cyclic GMP-AMP (cGAMP) synthase (cGAS) produces the cyclic dinucleotide cGAMP, which activates \{STING\} to trigger a type I interferon (IFN) response. We find that membrane fusion-inducing contact between donor cells expressing the \{HIV\} envelope (Env) and primary macrophages endogenously expressing the \{HIV\} receptor \{CD4\} and coreceptor enable intercellular transfer of cGAMP. This cGAMP exchange results in STING-dependent antiviral \{IFN\} responses in target macrophages and protection from \{HIV\} infection. Furthermore, under conditions allowing cell-to-cell transmission of HIV-1, infected primary T cells, but not cell-free virions, deliver cGAMP to autologous macrophages through HIV-1 Env and CD4/coreceptor-mediated membrane fusion sites and induce a STING-dependent, but cGAS-independent, \{IFN\} response in target cells. Collectively, these findings identify an infection-specific mode of horizontal transfer of cGAMP between primary immune cells that may boost antiviral responses, particularly in infected tissues in which cell-to-cell transmission of virions exceeds cell-free infection. }, added-at = {2016-10-17T13:10:24.000+0200}, author = {Xu, S and Ducroux, A and Ponnurangam, A and Vieyres, G and Franz, S and Müsken, M and Zillinger, T and Malassa, A and Ewald, E and Hornung, V and Barchet, W and Häussler, S and Pietschmann, T and Goffinet, C}, biburl = {https://www.bibsonomy.org/bibtex/2ce961f5d92817b29bdcf28439506a8ab/pietschmann}, editor = {Microbe, Cell Host}, interhash = {e7eda3700255c4cf2d8ba20d390730ce}, intrahash = {ce961f5d92817b29bdcf28439506a8ab}, journal = {Cell Host & Microbe }, keywords = {pietschmann}, number = 4, pages = {443-457}, pubmedurl = {https://www.ncbi.nlm.nih.gov/pubmed/27736643}, timestamp = {2016-10-17T13:10:24.000+0200}, title = {cGAS-Mediated Innate Immunity Spreads Intercellularly through HIV-1 Env-Induced Membrane Fusion Sites }, volume = 20, year = 2016 }