2011
DOI: 10.1016/j.ijom.2011.07.669
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Differential regulation of proteoglycan 4 by IL-1alpha and TGF-beta1 in rat condylar chondrocytes

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Cited by 3 publications
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“…Studies in fibroblasts suggest that CTGF is a down-stream mediator of TGFb1-induced collagen synthesis (Grotendorst et al 1996;Duncan et al 1999). It was previously reported that PRG4 expression is positively regulated by exogenously added TGF-beta1 and negatively regulated by IL-1beta in cultured cells (Lee et al 2008;Cheng et al 2010). Therefore, we hypothesized that decreased PRG4 mRNA and protein expression detected in our study in tendons of old rats could be mediated by the decrease in TGFb1 and CTGF expression.…”
Section: Discussionmentioning
confidence: 62%
“…Studies in fibroblasts suggest that CTGF is a down-stream mediator of TGFb1-induced collagen synthesis (Grotendorst et al 1996;Duncan et al 1999). It was previously reported that PRG4 expression is positively regulated by exogenously added TGF-beta1 and negatively regulated by IL-1beta in cultured cells (Lee et al 2008;Cheng et al 2010). Therefore, we hypothesized that decreased PRG4 mRNA and protein expression detected in our study in tendons of old rats could be mediated by the decrease in TGFb1 and CTGF expression.…”
Section: Discussionmentioning
confidence: 62%
“…TGF-b's have been shown to stimulate PRG4 production in chondrocytes, 34,[41][42][43] as well as infrapateller fat pad progenitor cells. 44 MSCs in alginate culture secrete PRG4, 19 however factors which stimulate or regulate this production are unknown.…”
Section: Discussionmentioning
confidence: 99%
“…It is non-invasive and results in rapid patient response. Earlier studies showed that during the occurrence and development of TMD, cytokines such as IL-1, IL-6, and TNF-a are involved in inflammation of the synovium, leading to destruction of articular cartilage and excessive apoptosis of chondrocytes in the soft tissue of bone and joints as a result of increased NO content and the imbalance of local metabolism in the joint [23][24][25]. ESW can reduce NO content in the articular fluid, reduce the apoptosis of chondrocytes, promote the proliferation of articular cartilage and the repair of cartilage defects, and inhibit the secretion of inflammatory cytokines [26,27].…”
Section: Discussionmentioning
confidence: 99%