| Literature DB >> 27980033 |
Eugene Drokhlyansky1,2,3, Didem Göz Aytürk1,2,3, Timothy K Soh4, Ryan Chrenek1,2,3, Elaine O'Loughlin5, Charlotte Madore5, Oleg Butovsky5, Constance L Cepko6,2,3.
Abstract
The brain has a tightly regulated environment that protects neurons and limits inflammation, designated "immune privilege." However, there is not an absolute lack of an immune response. We tested the ability of the brain to initiate an innate immune response to a virus, which was directly injected into the brain parenchyma, and to determine whether this response could limit viral spread. We injected vesicular stomatitis virus (VSV), a transsynaptic tracer, or naturally occurring VSV-derived defective interfering particles (DIPs), into the caudate-putamen (CP) and scored for an innate immune response and inhibition of virus spread. We found that the brain parenchyma has a functional type I interferon (IFN) response that can limit VSV spread at both the inoculation site and among synaptically connected neurons. Furthermore, we characterized the response of microglia to VSV infection and found that infected microglia produced type I IFN and uninfected microglia induced an innate immune response following virus injection.Entities:
Keywords: VSV; brain; innate immunity; interferon; vesicular stomatitis virus
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Year: 2016 PMID: 27980033 PMCID: PMC5224383 DOI: 10.1073/pnas.1618157114
Source DB: PubMed Journal: Proc Natl Acad Sci U S A ISSN: 0027-8424 Impact factor: 11.205