首页> 外文期刊>Marine biotechnology >Regulation of Extracellular Matrix Synthesis by Shell Extracts from the Marine Bivalve Emphasis Type='Italic'>Pecten maximus/Emphasis> in Human Articular Chondrocytes— Application for Cartilage Engineering
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Regulation of Extracellular Matrix Synthesis by Shell Extracts from the Marine Bivalve Emphasis Type='Italic'>Pecten maximus/Emphasis> in Human Articular Chondrocytes— Application for Cartilage Engineering

机译:来自海洋双撇甲壳提取物的细胞外基质合成的调节

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The shells of the bivalve mollusks are organo-mineral structures predominantly composed of calcium carbonate, but also of a minor organic matrix, a mixture of proteins, glycoproteins, and polysaccharides. These proteins are involved in mineral deposition and, more generally, in the spatial organization of the shell crystallites in well-defined microstructures. In this work, we extracted different organic shell extracts (acid-soluble matrix, acid-insoluble matrix, water-soluble matrix, guanidine HCl/EDTA-extracted matrix, referred as ASM, AIM, WSM, and EDTAM, respectively) from the shell of the scallop Pecten maximus and studied their biological activities on human articular chondrocytes (HACs). We found that these extracts differentially modulate the biological activities of HACs, depending on the type of extraction and the concentration used. Furthermore, we showed that, unlike ASM and AIM, WSM promotes maintenance of the chondrocyte phenotype in monolayer culture. WSM increased the expression of chondrocyte-specific markers (aggrecan and type II collagen), without enhancing that of the main chondrocyte dedifferentiation marker (type I collagen). We also demonstrated that WSM could favor redifferentiation of chondrocyte in collagen sponge scaffold in hypoxia. Thus, this study suggests that the organic matrix of Pecten maximus , particularly WSM, may contain interesting molecules with chondrogenic effects. Our research emphasizes the potential use of WSM of Pecten maximus for cell therapy of cartilage.
机译:双子壳体的壳体是主要由碳酸钙组成的有机矿物结构,但也是少量有机基质,蛋白质,糖蛋白和多糖的混合物。这些蛋白质参与矿物沉积,更通常是在壳体微晶的空间组织中,在明确定义的微结构中。在这项工作中,我们从壳体中提取了不同的有机壳提取物(酸溶解基质,酸不溶性基质,水溶性基质,胍溶解的基质,分别称为ASM,AIM,WSM和EDTAM)扇贝Pecten Maximus的研究,并研究了他们对人关节软骨细胞(HACS)的生物学活性。我们发现这些提取物根据提取的类型和所用浓度的浓度来差异地调节HACS的生物活性。此外,我们表明,与ASM和AIM不同,WSM促进单层培养中软骨细胞表型的维持。 WSM增加了特异性细胞特异性标记物(藻类和II型胶原蛋白)的表达,而不提高了主要的软骨细胞消除剂标志物(I型胶原蛋白)。我们还表明,WSM可以赞成缺氧中胶原蛋白海绵支架的软骨细胞的重新细胞。因此,该研究表明,Pecten Maximus,特别是WSM的有机基质可含有有趣的分子,具有有性化的效果。我们的研究强调了Pecten Maximus WSM的潜在用途,用于软骨细胞疗法。

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