Involvement of p63 in the <it>herpes simplex virus</it>-1-induced demise of corneal cells

<p>Abstract</p> <p>Background</p> <p>The transcription factor p63 plays a pivotal role in the development and maintenance of epithelial tissues, including the ocular surface. In an effort to gain insight into the pathogenesis of keratitis caused by HSV-1, we determined...

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Main Authors: Mándi Yvette, Kemény Lajos, Gallyas Éva, Orosz László, Facskó Andrea, Megyeri Klára
Format: Article
Language:English
Published: BMC 2010-06-01
Series:Journal of Biomedical Science
Online Access:http://www.jbiomedsci.com/content/17/1/47
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spelling doaj-3d1f47ceb162402b84eff06eb88a80332020-11-24T23:58:13ZengBMCJournal of Biomedical Science1021-77701423-01272010-06-011714710.1186/1423-0127-17-47Involvement of p63 in the <it>herpes simplex virus</it>-1-induced demise of corneal cellsMándi YvetteKemény LajosGallyas ÉvaOrosz LászlóFacskó AndreaMegyeri Klára<p>Abstract</p> <p>Background</p> <p>The transcription factor p63 plays a pivotal role in the development and maintenance of epithelial tissues, including the ocular surface. In an effort to gain insight into the pathogenesis of keratitis caused by HSV-1, we determined the expression patterns of the p63 and Bax proteins in the Staatens Seruminstitute Rabbit Cornea cell line (SIRC).</p> <p>Methods</p> <p>SIRC cells were infected with HSV-1 at various multiplicities and maintained for different periods of time. Virus replication was measured by indirect immunofluorescence assay and Western blot analysis. Cell viability was determined by MTT assay. The apoptotic response of the infected cells was quantified by ELISA detecting the enrichment of nucleosomes in the cytoplasm. Western blot analysis was used to determine the levels of p63 and Bax proteins.</p> <p>Results</p> <p>Indirect immunofluorescence assays and Western blot analyses demonstrated the presence of HSV-1 glycoprotein D (gD) in the infected SIRC cell line, and the pattern of gD expression was consistent with efficient viral replication. The results of MTT and ELISA assays showed that HSV-1 elicited a strong cytopathic effect, and apoptosis played an important role in the demise of the infected cells. Mock-infected SIRC cells displayed the constitutive expression of ΔNp63α. The expressions of the Bax-β and TAp63γ isoforms were considerably increased, whereas the level of ΔNp63α was decreased in the HSV-1-infected SIRC cells. Experiments involving the use of acyclovir showed that viral DNA replication was necessary for the accumulation of TAp63γ.</p> <p>Conclusion</p> <p>These data suggest that a direct, virus-mediated cytopathic effect may play an important role in the pathogenic mechanism of herpetic keratitis. By disturbing the delicate balance between the pro-survival ΔN and the pro-apoptotic TA isoforms, HSV-1 may cause profound alterations in the viability of the ocular cells and in the tissue homeostasis of the ocular surface.</p> http://www.jbiomedsci.com/content/17/1/47
collection DOAJ
language English
format Article
sources DOAJ
author Mándi Yvette
Kemény Lajos
Gallyas Éva
Orosz László
Facskó Andrea
Megyeri Klára
spellingShingle Mándi Yvette
Kemény Lajos
Gallyas Éva
Orosz László
Facskó Andrea
Megyeri Klára
Involvement of p63 in the <it>herpes simplex virus</it>-1-induced demise of corneal cells
Journal of Biomedical Science
author_facet Mándi Yvette
Kemény Lajos
Gallyas Éva
Orosz László
Facskó Andrea
Megyeri Klára
author_sort Mándi Yvette
title Involvement of p63 in the <it>herpes simplex virus</it>-1-induced demise of corneal cells
title_short Involvement of p63 in the <it>herpes simplex virus</it>-1-induced demise of corneal cells
title_full Involvement of p63 in the <it>herpes simplex virus</it>-1-induced demise of corneal cells
title_fullStr Involvement of p63 in the <it>herpes simplex virus</it>-1-induced demise of corneal cells
title_full_unstemmed Involvement of p63 in the <it>herpes simplex virus</it>-1-induced demise of corneal cells
title_sort involvement of p63 in the <it>herpes simplex virus</it>-1-induced demise of corneal cells
publisher BMC
series Journal of Biomedical Science
issn 1021-7770
1423-0127
publishDate 2010-06-01
description <p>Abstract</p> <p>Background</p> <p>The transcription factor p63 plays a pivotal role in the development and maintenance of epithelial tissues, including the ocular surface. In an effort to gain insight into the pathogenesis of keratitis caused by HSV-1, we determined the expression patterns of the p63 and Bax proteins in the Staatens Seruminstitute Rabbit Cornea cell line (SIRC).</p> <p>Methods</p> <p>SIRC cells were infected with HSV-1 at various multiplicities and maintained for different periods of time. Virus replication was measured by indirect immunofluorescence assay and Western blot analysis. Cell viability was determined by MTT assay. The apoptotic response of the infected cells was quantified by ELISA detecting the enrichment of nucleosomes in the cytoplasm. Western blot analysis was used to determine the levels of p63 and Bax proteins.</p> <p>Results</p> <p>Indirect immunofluorescence assays and Western blot analyses demonstrated the presence of HSV-1 glycoprotein D (gD) in the infected SIRC cell line, and the pattern of gD expression was consistent with efficient viral replication. The results of MTT and ELISA assays showed that HSV-1 elicited a strong cytopathic effect, and apoptosis played an important role in the demise of the infected cells. Mock-infected SIRC cells displayed the constitutive expression of ΔNp63α. The expressions of the Bax-β and TAp63γ isoforms were considerably increased, whereas the level of ΔNp63α was decreased in the HSV-1-infected SIRC cells. Experiments involving the use of acyclovir showed that viral DNA replication was necessary for the accumulation of TAp63γ.</p> <p>Conclusion</p> <p>These data suggest that a direct, virus-mediated cytopathic effect may play an important role in the pathogenic mechanism of herpetic keratitis. By disturbing the delicate balance between the pro-survival ΔN and the pro-apoptotic TA isoforms, HSV-1 may cause profound alterations in the viability of the ocular cells and in the tissue homeostasis of the ocular surface.</p>
url http://www.jbiomedsci.com/content/17/1/47
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