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Designer Self-Assembling Peptide Nanofiber Scaffolds Containing Link Protein N-Terminal Peptide Induce Chondrogenesis of Rabbit Bone Marrow Stem Cells

机译:含有链接蛋白N-末端肽的设计者自组装肽纳米纤维支架诱导兔骨髓干细胞的软骨发生

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摘要

Designer self-assembling peptide nanofiber hydrogel scaffolds have been considered as promising biomaterials for tissue engineering because of their excellent biocompatibility and biofunctionality. Our previous studies have shown that a novel designer functionalized self-assembling peptide nanofiber hydrogel scaffold (RLN/RADA16, LN-NS) containing N-terminal peptide sequence of link protein (link N) can promote nucleus pulposus cells (NPCs) adhesion and three-dimensional (3D) migration and stimulate biosynthesis of type II collagen and aggrecan by NPCs in vitro. The present study has extended these investigations to determine the effects of this functionalized LN-NS on bone marrow stem cells (BMSCs), a potential cell source for NP regeneration. Although the functionalized LN-NS cannot promote BMSCs proliferation, it significantly promotes BMSCs adhesion compared with that of the pure RADA16 hydrogel scaffold. Moreover, the functionalized LN-NS remarkably stimulates biosynthesis and deposition of type II collagen and aggrecan. These data demonstrate that the functionalized peptide nanofiber hydrogel scaffold containing link N peptide as a potential matrix substrate will be very useful in the NP tissue regeneration.
机译:设计师自组装纳米肽支架水凝胶已被视为有前途的,因为其优良的生物相容性和生物功能的组织工程生物材料。我们先前的研究已经表明,一种新颖的设计者官能自组装肽纳米纤维水凝胶支架(RLN / RADA16,LN-NS)包含链路蛋白(链路N)可以促进髓核细胞(NPC)的粘附性和三个N末端肽序列维(3D)迁移和刺激II型胶原的生物合成,并通过在体外的NPC聚集蛋白聚糖。本研究中已扩展了这些调查,以确定该官能LN-NS对骨髓干细胞(BMSC)的影响,对于NP再生潜在的细胞来源。虽然官能LN-NS不能促进BMSCs增殖,它显著与纯RADA16水凝胶支架相比促进骨髓基质细胞的粘附力。此外,官能化LN-NS显着刺激生物合成和II型胶原和软骨聚集蛋白聚糖的沉积。这些数据表明,所述官能化的肽纳米纤维水凝胶支架包含连结Ñ肽作为潜在的矩阵基板将在NP组织再生是非常有用的。

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