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Impact of Laminitis on the Canonical Wnt Signaling Pathway in Basal Epithelial Cells of the Equine Digital Laminae

机译:椎板炎对马数字层板基础上皮细胞中典型Wnt信号通路的影响

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摘要

The digital laminae is a two layer tissue that attaches the distal phalanx to the inner hoof wall, thus suspending the horse's axial skeleton in the hoof capsule. This tissue fails at the epidermal:dermal junction in laminitic horses, causing crippling disease. Basal epithelial cells line the laminar epidermal:dermal junction, undergo physiological change in laminitic horses, and lose versican gene expression. Versican gene expression is purportedly under control of the canonical Wnt signaling pathway and is a trigger for mesenchymal-to-epithelial transition; thus, its repression in laminar epithelial cells of laminitic horses may be associated with suppression of the canonical Wnt signaling pathway and loss of the epithelial cell phenotype. In support of the former contention, we show, using laminae from healthy horses and horses with carbohydrate overload-induced laminitis, quantitative real-time polymerase chain reaction, Western blotting after sodium dodecylsulfate polyacrylamide gel electrophoresis, and immunofluorescent tissue staining, that positive and negative regulatory components of the canonical Wnt signaling pathway are expressed in laminar basal epithelial cells of healthy horses. Furthermore, expression of positive regulators is suppressed and negative regulators elevated in laminae of laminitic compared to healthy horses. We also show that versican gene expression in the epithelial cells correlates positively with that of β-catenin and T-cell Factor 4, consistent with regulation by the canonical Wnt signaling pathway. In addition, gene and protein expression of β-catenin correlates positively with that of integrin β4 and both are strongly suppressed in laminar basal epithelial cells of laminitic horses, which remain E-cadherin+/vimentin, excluding mesenchymal transition as contributing to loss of the adherens junction and hemidesmosome components. We propose that suppression of the canonical Wnt signaling pathway, and accompanying reduced expression of β catenin and integrin β4 in laminar basal epithelial cells reduces cell:cell and cell:basement membrane attachment, thus, destabilizing the laminar epidermal:dermal junction.
机译:数字薄片是两层组织,将远端指骨附在蹄壁内侧,从而将马的轴向骨骼悬挂在蹄囊中。该组织在拉皮马的表皮:真皮交界处失效,从而导致致残性疾病。基底上皮细胞排列在层状表皮:真皮交界处,在层状马中发生生理变化,并失去versican基因表达。 Versican基因的表达据称在经典的Wnt信号传导通路的控制下,是间质向上皮转化的触发因素。因此,其在层状马的层状上皮细胞中的抑制作用可能与规范的Wnt信号通路的抑制和上皮细胞表型的丧失有关。为了支持前一种观点,我们使用健康马匹和患有碳水化合物超负荷引起的马鞭毛炎的马匹的片层,定量实时聚合酶链反应,十二烷基硫酸钠聚丙烯酰胺凝胶电泳后的免疫印迹和免疫荧光组织染色显示了阳性和阴性正常Wnt信号通路的调节成分在健康马的层状基底上皮细胞中表达。此外,与健康马匹相比,在椎板动物的椎板中正调控子的表达受到抑制,负调控子升高。我们还显示,上皮细胞中的versican基因表达与β-catenin和T细胞因子4呈正相关,与经典Wnt信号通路的调控一致。此外,β-catenin的基因和蛋白质表达与整联蛋白β4呈正相关,并且在层状马的层状基底上皮细胞中均被强烈抑制,这些细胞仍为E-cadherin + / vimentin -,不包括间充质转变,因为其导致粘附连接和半桥粒成分的损失。我们建议抑制规范的Wnt信号通路,并伴随层状基底上皮细胞中βcatenin和整联蛋白β4的表达减少,从而减少细胞:细胞和细胞:基底膜的附着,从而破坏层状表皮:真皮连接。

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