| Literature DB >> 25762734 |
Susanne Himmelein1, Anja Lindemann2, Inga Sinicina3, Michael Strupp2, Thomas Brandt4, Katharina Hüfner2.
Abstract
Herpes simplex virus 1 (HSV-1) can establish lifelong latency in human trigeminal ganglia. Latently infected ganglia contain CD8(+) T cells, which secrete granzyme B and are thus capable of inducing neuronal apoptosis. Using immunohistochemistry and single-cell reverse transcription-quantitative PCR (RT-qPCR), higher frequency and transcript levels of caspase-3 were found in HSV-1-negative compared to HSV-1-positive ganglia and neurons, respectively. No terminal deoxynucleotidyltransferase-mediated dUTP-biotin nick end labeling (TUNEL) assay-positive neurons were detected. The infiltrating T cells do not induce apoptosis in latently infected neurons.Entities:
Mesh:
Substances:
Year: 2015 PMID: 25762734 PMCID: PMC4442501 DOI: 10.1128/JVI.03481-14
Source DB: PubMed Journal: J Virol ISSN: 0022-538X Impact factor: 5.103