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High mobility group box chromosomal protein\u20101(<jats:styled-content style=\"fixed-case\">HMGB<\/jats:styled-content>\u20101)is a potent mediator of inflammation and the trigger of <jats:styled-content style=\"fixed-case\">OA<\/jats:styled-content>. The expression of <jats:styled-content style=\"fixed-case\">HMGB<\/jats:styled-content>\u20101 in <jats:styled-content style=\"fixed-case\">TMJ OA<\/jats:styled-content> was uncovered, but the role of <jats:styled-content style=\"fixed-case\">HMGB<\/jats:styled-content>\u20101 in <jats:styled-content style=\"fixed-case\">TMJ<\/jats:styled-content> cartilage degeneration is not fully understood. In this study, the regulation of <jats:styled-content style=\"fixed-case\">HMGB<\/jats:styled-content>\u20101 in <jats:styled-content style=\"fixed-case\">TMJ<\/jats:styled-content> condylar cartilage was revealed.<\/jats:p><\/jats:sec><jats:sec><jats:title>Methods<\/jats:title><jats:p>A complete Freund's adjuvant (<jats:styled-content style=\"fixed-case\">CFA<\/jats:styled-content>)\u2010induced <jats:styled-content style=\"fixed-case\">TMJ<\/jats:styled-content> inflammation animal model was employed and the expression of <jats:styled-content style=\"fixed-case\">HMGB<\/jats:styled-content>\u20101 was detected at 1st, 2nd, and 6th weeks by immunohistochemistry. <jats:styled-content style=\"fixed-case\">TMJ<\/jats:styled-content> condylar chondrocytes were incubated with <jats:styled-content style=\"fixed-case\">IL<\/jats:styled-content>\u20101\u03b2 (10 and 40 ng\/ml) at 24, 48, and 72 h, and the translocation and protein level of <jats:styled-content style=\"fixed-case\">HMGB<\/jats:styled-content>\u20101 were evaluated by immunofluorescence and Western blot.<\/jats:p><\/jats:sec><jats:sec><jats:title>Result<\/jats:title><jats:p>Nuclear <jats:styled-content style=\"fixed-case\">HMGB<\/jats:styled-content>\u20101 staining was predominantly located in chondrocytes of both the fibrosis and proliferative zones in healthy <jats:styled-content style=\"fixed-case\">TMJ<\/jats:styled-content>. 1st week and 2nd week after <jats:styled-content style=\"fixed-case\">CFA<\/jats:styled-content> injection, immunoreaction could be detected in the cytoplasms of <jats:styled-content style=\"fixed-case\">HMGB<\/jats:styled-content>\u20101\u2010positive cells and cartilage matrix especially in hypertrophic zone. At 6th week after <jats:styled-content style=\"fixed-case\">CFA<\/jats:styled-content> injection, cartilage matrix expression was disappeared and the cytoplasm expression of <jats:styled-content style=\"fixed-case\">HMGB<\/jats:styled-content>\u20101 was very weak in hypertrophic zone. <jats:styled-content style=\"fixed-case\">HMGB<\/jats:styled-content>\u20101 was translocated from the nucleus to the cytoplasm at 48 h after incubated with <jats:styled-content style=\"fixed-case\">IL<\/jats:styled-content>\u20101\u03b2 (10 ng\/ml and 40 ng\/ml). The protein level of <jats:styled-content style=\"fixed-case\">HMGB<\/jats:styled-content>\u20101 was increased after stimulation and had a peak at 48 h.<\/jats:p><\/jats:sec><jats:sec><jats:title>Conclusion<\/jats:title><jats:p><jats:styled-content style=\"fixed-case\">HMGB<\/jats:styled-content>\u20101 might be associated with <jats:styled-content style=\"fixed-case\">TMJ<\/jats:styled-content> inflammation and <jats:styled-content style=\"fixed-case\">OA<\/jats:styled-content>. Insight into the role of <jats:styled-content style=\"fixed-case\">HMGB<\/jats:styled-content>\u20101 in <jats:styled-content style=\"fixed-case\">TMJ<\/jats:styled-content> inflammation is helpful to add the new knowledge into the pathogenesis of <jats:styled-content style=\"fixed-case\">TMJ OA<\/jats:styled-content>.<\/jats:p><\/jats:sec>","DOI":"10.1111\/jop.12401","type":"journal-article","created":{"date-parts":[[2015,12,16]],"date-time":"2015-12-16T12:21:38Z","timestamp":1450268498000},"page":"539-545","source":"Crossref","is-referenced-by-count":15,"title":["<scp>IL<\/scp>\u20101\u03b2 mediating high mobility group box protein\u20101 expression in condylar chondrocyte during temporomandibular joint inflammation"],"prefix":"10.1111","volume":"45","author":[{"given":"Cheng","family":"Li","sequence":"first","affiliation":[{"name":"State Key Laboratory Breeding Base of Basic Science of Stomatology (Hubei\u2010MOST) &amp; Key Laboratory of Oral Biomedicine Ministry of Education 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