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Effect of RGD Peptide-Coated TiO2Nanotubes on the Attachment, Proliferation, and Functionality of Bone-Related Cells

机译:RGD肽包覆的TiO2纳米管对骨相关细胞的附着,增殖和功能的影响

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The purpose of this research was to characterize an Arg-Gly-Asp (RGD) peptide immobilized on TiO2nanotubes. In addition, we investigated the effects of the RGD peptide-coated TiO2nanotubes on the cellular response, proliferation, and functionality of osteogenic-induced human mesenchymal stem cells (hMSCs), which are osteoclasts that have been induced by bone marrow macrophages. The RGD peptide was grafted covalently onto the surface of TiO2nanotubes based on the results of SEM, FT-IR, and XPS. Furthermore, the RGD peptide promoted the initial attachment and proliferation of the hMSCs, regardless of the size of the TiO2nanotubes. However, the RGD peptide did not prominently affect the osteogenic functionality of the hMSCs because the peptide suppressed hMSC motility associated with osteogenic differentiation. The result of anin vitroosteoclast test showed that the RGD peptide accelerated the initial attachment of preosteoclasts and the formation of mature osteoclasts, which could resorb the bone matrix. Therefore, we believe that an RGD coating on TiO2nanotubes synthesized on Ti implants might not offer significant acceleration of bone formationin vivobecause osteoblasts and osteoclasts reside in the same compartment.
机译:这项研究的目的是表征固定在TiO2纳米管上的Arg-Gly-Asp(RGD)肽。此外,我们调查了RGD肽包覆的TiO2纳米管对成骨诱导的人间充质干细胞(hMSCs)的细胞应答,增殖和功能的影响,这些细胞是由骨髓巨噬细胞诱导的破骨细胞。根据SEM,FT-IR和XPS的结果,将RGD肽共价接枝到TiO2纳米管的表面。此外,无论TiO2纳米管的大小如何,RGD肽都能促进hMSC的初始附着和增殖。但是,RGD肽并未显着影响hMSC的成骨功能,因为该肽抑制了与成骨分化相关的hMSC运动。体外破骨细胞试验的结果表明,RGD肽加速了破骨细胞的初始附着和成熟的破骨细胞的形成,可以吸收骨基质。因此,我们认为,在钛植入物上合成的TiO2纳米管上的RGD涂层可能无法显着促进体内的骨形成,因为成骨细胞和破骨细胞位于同一隔间中。

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