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Latent herpes simplex virus 1 infection does not induce apoptosis in human trigeminal Ganglia.


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.

SUBMITTER: Himmelein S 

PROVIDER: S-EPMC4442501 | biostudies-literature | 2015 May

REPOSITORIES: biostudies-literature

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Latent herpes simplex virus 1 infection does not induce apoptosis in human trigeminal Ganglia.

Himmelein Susanne S   Lindemann Anja A   Sinicina Inga I   Strupp Michael M   Brandt Thomas T   Hüfner Katharina K  

Journal of virology 20150311 10


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-media  ...[more]

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