首页> 外文期刊>Journal of Cell Science >Inhibition of basement membrane formation by a nidogen-binding laminin gamma 1-chain fragment in human skin-organotypic cocultures
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Inhibition of basement membrane formation by a nidogen-binding laminin gamma 1-chain fragment in human skin-organotypic cocultures

机译:结合抗原的层粘连蛋白γ1链片段在人类皮肤-有机型共培养物中抑制基底膜形成

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Basement membranes generally determine different tissue compartments in complex organs, such as skin, playing not only an important structural but also a regulatory role. We have previously demonstrated the formation of a regular basement membrane in organotypic three-dimensional (3D)-cocultures of human skin keratinocytes and fibroblasts by indirect immunofluorescence and transmission electron microscopy. In this assembly process, cross-linking of type IV collagen and the laminin gamma1 chain by nidogen is considered a crucial step. For a functional proof, we have now competitively inhibited nidogen binding to laminin in 3D-cocultures with a recombinant laminin gamma1 fragment (gamma1III3-5 module) spanning this binding site. Repeated treatment abolished the deposition of nidogen at the epithelial-matrix interface but also greatly perturbed the presence of other matrix constituents such as laminin and perlecan. This effect persisted over the entire observation period of 10 to 21 days. In contrast, some components of the basement membrane zone were only moderately affected, with the laminin-5 isoform (gamma2 chain), type IV collagen and integrin alpha6beta4 still showing a distinct staining at their regular position, when seen by light microscopy. Furthermore, epidermal morphology and differentiation remained largely normal as indicated by the regular location of keratins K1/K10 and also of late differentiation markers. Ultrastructural examination demonstrated that the gamma1 fragment completely suppressed any formation of basement membrane structures (lamina densa) and also of hemidesmosomal adhesion complexes. As a consequence of hemidesmosome deficiency, keratin filament bundles were not attached to the ventral basal cell aspect. These findings were further substantiated by immuno-electron microscopy, revealing either loss or drastic reduction and dislocation of basement membrane and hemidesmosomal components. Taken together, in this simplified human skin model (representing a 'closed system') a functional link has been demonstrated between compound structures of the extra- and intracellular space at the junctional zone providing a basis to interfere at distinct points and in a controlled fashion.
机译:基底膜通常决定复杂器官(例如皮肤)中的不同组织区室,不仅起重要的结构作用,而且起调节作用。我们以前通过间接免疫荧光和透射电子显微镜在人皮肤角质形成细胞和成纤维细胞的器官型三维(3D)共培养中证明了规则基底膜的形成。在此组装过程中,通过胶原蛋白将IV型胶原蛋白和层粘连蛋白gamma1链交联被认为是至关重要的步骤。为了提供功能证明,我们现在通过跨层结合位点的重组层粘连蛋白gamma1片段(gamma1III3-5模块)在3D共培养中竞争性抑制了抗原原与层粘连蛋白的结合。重复处理消除了上皮-基质界面上的生原素沉积,但是也极大地干扰了层粘连蛋白和珍珠蛋白等其他基质成分的存在。这种效果在整个10到21天的观察期内一直持续。相反,当通过光学显微镜观察时,基底膜区的某些组件仅受到中等程度的影响,层粘连蛋白5亚型(γ2链),IV型胶原蛋白和整联蛋白α6β4在其正常位置仍显示出明显的染色。此外,如角蛋白K1 / K10和后期分化标记的规则位置所示,表皮形态和分化在很大程度上仍是正常的。超微结构检查表明,γ1片段完全抑制了基底膜结构(lamina densa)的任何形成以及半桥粒粘附复合物的形成。由于半桥粒缺乏,角蛋白丝​​束未附着于腹侧基底细胞方面。免疫电子显微镜进一步证实了这些发现,揭示了基膜和半桥粒成分的丢失或急剧减少和错位。综上所述,在这种简化的人类皮肤模型(代表“封闭系统”)中,在连接区的细胞外空间和细胞内空间的复合结构之间已证明了功能性联系,从而为以不同方式干预不同点提供了基础。

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