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Histone acetylation modulates influenza virus replicative intermediate dsRNA-induced interleukin-6 expression in A549 cells / 南方医科大学学报
Journal of Southern Medical University ; (12): 282-286, 2013.
Artículo en Chino | WPRIM | ID: wpr-322063
ABSTRACT
<p><b>OBJECTIVE</b>To investigate the role of histone acetylation in regulating influenza virus replicative intermediate double-stranded RNA (dsRNA)-induced interleukin-6 (IL-6) expression in A549 cells.</p><p><b>METHODS</b>A549 cells were treated with influenza virus replicative intermediate dsRNA, histone deacetylase (HDAC) inhibitor trichostatin A (TSA), or HADC small interfering RNA (siRNA). The changes in the cellular IL-6 promoter activities were detected by dual-luciferase assay, and IL-6 mRNA and protein expressions in the cells were determined using real-time RT-PCR and ELISA, respectively.</p><p><b>RESULTS</b>Influenza virus replicative intermediate dsRNA obviously up-regulated IL-6 expression in the cells. HDAC inhibitor TSA significantly enhanced the activity of IL-6 promoter and increased IL-6 mRNA expression in A549 cells, and HDAC3 may play an important role in this process. HDAC inhibitor TSA and DNMT inhibitor DAC showed no synergic effect in regulating IL-6 expression.</p><p><b>CONCLUSIONS</b>Influenza virus replicative intermediate dsRNA-induced IL-6 expression in A549 cells is regulated by histone acetylation.</p>
Asunto(s)
Texto completo: Disponible Índice: WPRIM (Pacífico Occidental) Asunto principal: Orthomyxoviridae / Farmacología / Acetilación / ARN Bicatenario / ARN Mensajero / ARN Viral / Histonas / Regulación de la Expresión Génica / Interleucina-6 / Regiones Promotoras Genéticas Límite: Humanos Idioma: Chino Revista: Journal of Southern Medical University Año: 2013 Tipo del documento: Artículo

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Texto completo: Disponible Índice: WPRIM (Pacífico Occidental) Asunto principal: Orthomyxoviridae / Farmacología / Acetilación / ARN Bicatenario / ARN Mensajero / ARN Viral / Histonas / Regulación de la Expresión Génica / Interleucina-6 / Regiones Promotoras Genéticas Límite: Humanos Idioma: Chino Revista: Journal of Southern Medical University Año: 2013 Tipo del documento: Artículo