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dc.contributor.authorNawarat Viriyakhasemen_US
dc.contributor.authorSiriprapa Khuajanen_US
dc.contributor.authorPrachya Kongtawelerten_US
dc.contributor.authorAmpai Panthongen_US
dc.contributor.authorSiriwan Ongchaien_US
dc.contributor.authorVichai Reutrakulen_US
dc.date.accessioned2018-09-04T09:45:52Z-
dc.date.available2018-09-04T09:45:52Z-
dc.date.issued2014-01-01en_US
dc.identifier.issn10712690en_US
dc.identifier.other2-s2.0-84937109779en_US
dc.identifier.other10.1007/s11626-014-9777-7en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84937109779&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/53252-
dc.description.abstract© 2014, The Society for In Vitro Biology. The present study aimed to demonstrate the phenomena of hyaluronan synthesis in response to lipopolysaccharide-induced inflammation in SW982, a human synovial sarcoma cell line. The expression of IL-1ß, including Toll-like receptor 4 and IL-1ß-converting enzyme, was proved to be induced by a reverse transcription-polymerase chain reaction. The expression of HAS genes encoding enzyme hyaluronan synthase 2 and 3, including CD44 gene which encodes the cell surface receptor of hyaluronan were upregulated in association with the activation of inflammation, along with an increase in hyaluronan level in the culture medium. The highest expression of HAS2 and HAS3 was found at 9 h after treatment with lipopolysaccharide. However, HAS1 gene expression was not detectable neither with the non-treatment nor with the treatment with lipopolysaccharide. Dexamethasone at 30 nM significantly suppressed lipopolysaccharide-induced HAS genes expression, leading to the decline of the hyaluronan level in the culture medium. Our results demonstrated the effective tool for studying hyaluronan synthesis in association with inflammation in the SW982 cell line.en_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.subjectMedicineen_US
dc.titleIn vitro model of hyaluronan synthase gene expression associated with lipopolysaccharide-induced inflammation in SW982 cell lineen_US
dc.typeJournalen_US
article.title.sourcetitleIn Vitro Cellular and Developmental Biology - Animalen_US
article.volume50en_US
article.stream.affiliationsChiang Mai Universityen_US
article.stream.affiliationsMahidol Universityen_US
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