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首页> 外文期刊>The Journal of investigative dermatology. >Plakoglobin but not desmoplakin regulates keratinocyte cohesion via modulation of p38MAPK signaling
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Plakoglobin but not desmoplakin regulates keratinocyte cohesion via modulation of p38MAPK signaling

机译:血浆珠蛋白而非去氨铂蛋白通过调节p38MAPK信号传导来调节角质形成细胞的凝聚力

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摘要

Plakoglobin (Pg) and desmoplakin (DP) are adapter proteins within the desmosome, providing a mechanical link between desmosomal cadherins as transmembrane adhesion molecules and the intermediate filament cytoskeleton. As in the severe skin blistering disease pemphigus, autoantibodies against desmosomal adhesion molecules induce loss of keratinocyte cohesion at least in part via p38 mitogen-activated protein kinase (p38MAPK) activation and depletion of desmosomal components, we evaluated the roles of Pg and DP in the p38MAPK-dependent loss of cell adhesion. Silencing of either Pg or DP reduced cohesion of cultured human keratinocytes in dissociation assays. However, Pg but not DP silencing caused activation of p38MAPK-dependent keratin filament collapse and cell dissociation. Interestingly, extranuclear but not nuclear Pg rescued loss of cell adhesion and keratin retraction. In line with this, Pg regulated the levels of the desmosomal adhesion molecule desmoglein 3 and tethered p38MAPK to desmosomal complexes. Our data demonstrate a role of extranuclear Pg in controlling cell adhesion via p38MAPK-dependent regulation of keratin filament organization.
机译:Plagloglobin(Pg)和desmoplakin(DP)是desmosome中的衔接蛋白,可在作为跨膜粘附分子的desmosomal cadherins与中间丝细胞骨架之间提供机械连接。与严重的皮肤水疱性疾病天疱疮一样,针对桥粒粘附分子的自身抗体至少部分通过p38促分裂原活化蛋白激酶(p38MAPK)活化和桥粒成分的消耗诱导角质形成细胞内聚力的丧失,我们评估了Pg和DP在桥粒中的作用。 p38MAPK依赖的细胞粘附丧失。在解离分析中,Pg或DP的沉默会降低培养的人角质形成细胞的凝聚力。然而,Pg而非DP沉默导致激活p38MAPK依赖性角蛋白丝塌陷和细胞解离。有趣的是,核外Pg而非核Pg可以挽救细胞粘附力的丧失和角蛋白的收缩。与此相一致,Pg调节了桥粒粘附分子桥粒芯蛋白3的水平以及将p38MAPK束缚在桥粒复合物中。我们的数据表明核外Pg通过依赖p38MAPK的角蛋白丝组织的调控来控制细胞粘附。

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