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首页> 外文期刊>Biomacromolecules >Bone-Like Mineral Nucleating Peptide Nanofibers Induce Differentiation of Human Mesenchymal Stem Cells into Mature Osteoblasts
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Bone-Like Mineral Nucleating Peptide Nanofibers Induce Differentiation of Human Mesenchymal Stem Cells into Mature Osteoblasts

机译:类骨矿物核肽纳米纤维诱导人间充质干细胞分化为成熟成骨细胞。

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A bone implant should integrate to the tissue through a bone-like mineralized interface, which requires increased osteoblast activity at the implant—tissue boundary. Modification of the implant surface with synthetic bioinstructive cues facilitates on-site differentiation of progenitor stem cells to functional mature osteoblasts and results in subsequent mineralization. Inspired by the bioactive domains of the borie extracellular matrix proteins and the mussel adhesive proteins, we synthesized peptide nanofibers to promote bone-like mineralization on the implant surface. Nanofibers functionalized with osteoinductive collagen I derived Asp-Gly-Glu-Ala (DGEA) peptide sequence provide an advantage in initial adhesion, spreading, and early commitment to osteogenic differentiation for mesenchymal stem cells (hMSCs). In this study, we demonstrated that this early osteogenic commitment, however, does not necessarily guarantee a priority for maturation into functional osteoblasts. Similar to natural biological cascades, early commitment should be further supported with additional signals to provide a long-term effect on differentiation. Here, we showed that peptide nanofibers functionalized with Glu-Glu-Glu (EEE) sequence enhanced mineralization abilities due to osteoinductive properties for late-stage differentiation of hMSCs. Mussel-inspired functionalization not only enables robust immobilization on metal surfaces, but also improves bone-like mineralization under physiologically simulated conditions. The multifunctional osteoinductive peptide nanofiber biointerfaces presented here facilitate osseointegration for long-term clinical stability.
机译:骨植入物应通过骨状矿化界面整合到组织中,这需要增加植入物(组织边界)处的成骨细胞活性。用合成的生物指示剂修饰植入物表面有助于将祖细胞干细胞原位分化为功能成熟的成骨细胞,并导致随后的矿化。受鲍里细胞外基质蛋白和贻贝粘附蛋白的生物活性域的启发,我们合成了肽纳米纤维以促进植入物表面的骨样矿化。用衍生自骨诱导性胶原I的Asp-Gly-Glu-Ala(DGEA)肽序列功能化的纳米纤维在间充质干细胞(hMSCs)的初始粘附,铺展和早期致骨分化方面提供了优势。在这项研究中,我们证明了这种早期的成骨作用并不一定能保证将其成熟为功能性成骨细胞。与自然生物级联反应相似,应通过其他信号进一步支持早期承诺,以对分化产生长期影响。在这里,我们显示,由于hMSCs后期分化的骨诱导特性,用Glu-Glu-Glu(EEE)序列功能化的肽纳米纤维增强了矿化能力。贻贝启发的功能化不仅能够将其牢固地固定在金属表面上,而且可以在生理模拟条件下改善骨样矿化作用。此处介绍的多功能骨诱导肽纳米纤维生物界面有助于骨整合以实现长期临床稳定性。

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