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Cell-matrix interactions of in vitro human skin fibroblasts upon addition of hyaluronan.

机译:添加透明质酸后体外人皮肤成纤维细胞的细胞-基质相互作用。

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Normal human skin fibroblasts were grown in a three-dimensional collagen gel or in monolayer in the presence or absence of high molecular weight hyaluronan (HA) to assess the influence of extracellular HA on cell-matrix interactions. HA incorporated into the collagen gel or added to the culture medium did not modify lattice retraction with time. The effect was independent from HA molecular weight (from 7.5x10(5) to 2.7x10(6)Da) and concentration (from 0.1 up to 1mg/ml). HA did not affect shape and distribution of fibroblasts within the gel, whereas it induced the actin filaments to organise into thicker cables running underneath the plasma membrane. The same phenomenon was observed in fibroblasts grown in monolayer. By contrast, vimentin cytoskeleton and cell-substrate focal adhesions were not modified by exogenous HA. The number of fibroblasts attached to HA-coated dishes was always significantly lower compared to plastic and to collagen type I-coated plates. By contrast, adhesion was not affected by soluble HA added to the medium nor by anti-CD44 and anti-RHAMM-IHABP polyclonals. After 24-h seeding on collagen type I or on plastic, cells were large and spread. Conversely, cells adherent to HA-coated surfaces were long, thin and aligned into rows; alcian blue showed that cells were attached to the plastic in between HA bundles.Therefore, normal human skin fibroblasts exhibit very scarce, if any, adhesion to matrix HA, either soluble or immobilised. Moreover, even at high concentration, HA molecules do not exert any visco-mechanical effect on lattice retraction and do not interfere with fibroblast-collagen interactions nor with focal adhesion contacts of fibroblasts with the substrate. This is probably relevant in organogenesis and wound repair. By contrast, HA greatly modifies the organisation of the actin cytoskeleton, suggesting that CD44-mediated signal transduction by HA may affect cell locomotion and orientation, as indicated by the fusiform shape of fibroblasts grown in the presence of immobilised HA. A role of HA in cell orientation could be relevant for the deposition of collagen fibrils in regeneration and tissue remodelling.
机译:在存在或不存在高分子量透明质酸(HA)的情况下,正常人皮肤成纤维细胞在三维胶原蛋白凝胶中或单层生长,以评估细胞外HA对细胞-基质相互作用的影响。掺入胶原蛋白凝胶中或添加到培养基中的HA不会随时间改变晶格收缩。该效果与HA分子量(从7.5x10(5)到2.7x10(6)Da)和浓度(从0.1到1mg / ml)无关。 HA不会影响凝胶中成纤维细胞的形状和分布,而会诱导肌动蛋白丝组织成在质膜下延伸的较粗电缆。在单层生长的成纤维细胞中观察到相同的现象。相比之下,波形蛋白的细胞骨架和细胞底物的粘着粘附并未被外源性HA修饰。与塑料和I型胶原涂层板相比,附着在HA涂层培养皿上的成纤维细胞数量始终显着降低。相比之下,粘附不受添加到培养基中的可溶性HA的影响,也不受抗CD44和抗RHAMM-IHABP多克隆的影响。在I型胶原蛋白或塑料上播种24小时后,细胞变大并扩散。相反,粘附在HA涂层表面的细胞又长又薄,排列成行。阿尔辛蓝表明细胞附着在HA束之间的塑料上,因此,正常人皮肤成纤维细胞对可溶或固定化的HA的粘附力非常有限(如果有的话)。此外,即使在高浓度下,HA分子也不会对晶格收缩产生任何粘机械作用,也不会干扰成纤维细胞-胶原蛋白的相互作用,也不会干扰成纤维细胞与基质的粘着接触。这可能与器官发生和伤口修复有关。相比之下,HA极大地改变了肌动蛋白细胞骨架的组织,表明HA进行的CD44介导的信号转导可能影响细胞的运动和方向,如在固定化HA存在下生长的成纤维细胞的梭形形状所表明的那样。 HA在细胞定向中的作用可能与胶原纤维在再生和组织重塑中的沉积有关。

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