TITLE

The Roles of Inflammation, STAT Transcription Factors, and Nerve Growth Factor in Viral Reactivation and Herpes Keratitis

AUTHOR(S)
Kriesel, John D.
PUB. DATE
May 2002
SOURCE
DNA & Cell Biology;May2002, Vol. 21 Issue 5/6, p475
SOURCE TYPE
Academic Journal
DOC. TYPE
Article
ABSTRACT
Nerve growth factor (NGF) has an inhibitory effect while inflammatory cytokines may stimulate herpes simplex virus (HSV) reactivation. NGF binds to its receptor trkA on terminal axons and signals the neuron cell body in the ganglion. Many cytokines may also signal neurons through their specific receptors, affecting STAT transcription factors within the cell bodies. We studied the effects of trigeminal ganglion (TG) explantation, a powerful HSV reactivation stimulus, on the NGF/trkA and the JAK/STAT signaling pathways. Immunohistochemistry and gel shifting experiments were performed using anti-STAT, anti-trkA, or negative control antibodies on mouse TGs. The expression of neuronal trkA was greatly reduced or eliminated by 3 days postexplantation. In contrast, the expression of STAT1, STAT3, and STAT5b, as well as phosphotyrosine-STAT3 were relatively preserved in these explanted TGs. Gel-shifting experiments indicated that TG nuclear extracts bind specifically to the HSV-1 LAT promoter, an important viral gene that regulates reactivation. STAT1, but not STAT3 or STAT5b, was detected as a component of this LAT binding complex. These studies suggest that the inhibitory effects of NGF/trkA signaling are lost after TG explantation while STAT expression is maintained, allowing HSV-1 reactivation to proceed.
ACCESSION #
7008877

 

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