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Roles of calcium phosphate-mediated integrin expression and MAPK signaling pathways in the osteoblastic differentiation of mesenchymal stem cells

机译:磷酸钙介导的整合素表达和MAPK信号通路在间充质干细胞成骨细胞分化中的作用

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Osteoinduction of calcium phosphate (CaP) ceramics has been widely confirmed and accepted, but the underlying mechanism has not been fully elucidated. This study investigates the early biomolecular events that contributed to the transduction of extracellular material cues outside in, when MSCs were cultured in osteoinductive biphasic calcium phosphate (BCP) ceramics, and explores their roles in BCP-induced osteogenesis. The results demonstrated that BCP ceramics had a strong adsorption affinity for serum proteins, which might favor cell adhesion and mediate the expression of the cell surface receptor - integrin. qRT-PCR analysis found that BCP ceramics significantly up-regulated integrin alpha(2) and alpha(3) genes under both in vitro and in vivo conditions. As integrins clustered together into focal contacts (cell adhesion sites), immunofluorescence staining showed that compared to glass surfaces, cells seeded in BCP ceramics formed a relatively short focal contact and exhibited a smaller cell size. Moreover, western blotting analysis indicated that BCP ceramics could activate down-stream MAPK signaling pathways, whereas blockage of either ERK or P38 signals could dramatically attenuate BCP-induced osteogenesis. These findings suggested that BCP ceramics might mediate cell adhesion through transmembrane proteins - integrins - to realize the transduction of "outside-in signaling'', and subsequently trigger the intracellular MAPK signaling cascade to induce the osteogenic differentiation of MSCs. They offered a promising principle for designing and fabricating tissue-inducing biomaterials to provide appropriate cues for target cells.
机译:磷酸钙(CaP)陶瓷的骨诱导已得到广泛证实和接受,但是其潜在机理尚未得到充分阐明。这项研究调查了早期的生物分子事件,当MSCs在骨诱导性双相磷酸钙(BCP)陶瓷中培养时,其有助于外界细胞外物质线索的转导,并探讨了它们在BCP诱导的成骨过程中的作用。结果表明BCP陶瓷对血清蛋白具有很强的吸附亲和力,这可能有助于细胞粘附并介导细胞表面受体整合素的表达。 qRT-PCR分析发现,在体外和体内条件下,BCP陶瓷均显着上调整联蛋白alpha(2)和alpha(3)基因。由于整联蛋白聚集在一起形成焦点接触(细胞粘附位点),免疫荧光染色显示,与玻璃表面相比,接种在BCP陶瓷中的细胞形成了相对较短的焦点接触,并显示出较小的细胞大小。此外,蛋白质印迹分析表明,BCP陶瓷可以激活下游MAPK信号通路,而ERK或P38信号的阻滞则可以显着减弱BCP诱导的成骨作用。这些发现提示BCP陶瓷可能通过跨膜蛋白-整合素介导细胞粘附,从而实现“外向内信号转导”的转导,并随后触发细胞内MAPK信号级联反应诱导MSCs的成骨分化。用于设计和制造诱导组织的生物材料,以为靶细胞提供适当的提示。

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