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Stable biofunctionalization of hydroxyapatite (HA) surfaces by HA-binding/osteogenic modular peptides for inducing osteogenic differentiation of mesenchymal stem cells

机译:HA结合/成骨模块肽对羟基磷灰石(HA)表面的稳定生物功能化以诱导间充质干细胞的成骨分化

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摘要

Hydroxyapatite (HA), the principal component of bone mineral, shows osteoconductive properties when employed for coating metal implants as well as scaffold materials in synthetic bone grafts. With the goal of providing this material with osteoinductive capabilities to promote faster bone regeneration, we show an easy approach to functionalize HA implant surfaces and enrich them with osteoinductive properties by the use of HA-binding modular peptides. The modular peptides are designed as a combination of two domains, an HA-binding peptide motif and an osteogenic peptide motif derived from the osteogenic growth peptide (OGP) or bone morphometric protein 7 (BMP-7). To identify the best HA-binding peptide, several nature-inspired peptides derived from natural bone extracellular matrix proteins (bone sialoprotein, osteonectin, osteocalcin, and salivarin statherin) were compared for HA-binding activity, revealing concentration-dependent and incubation-time-dependent behaviours. We discovered that a Poly-E heptamer (E7) is the best HA-binding peptide, and thus combined it with a second osteogenic peptidic domain to create an osteoinductive modular peptide. After binding/release characterization, we found that the addition of the second osteogenic peptide domain did not change the binding profile of the modular peptides and caused only a slight change in their release kinetics. Mesenchymal stem cells (MSCs) were cultured on the HA substrates functionalized with modular peptides, and cell adhesion, proliferation, and differentiation in a basal medium (i.e., without any osteogenic supplements) were investigated. Gene expression data clearly showed that MSCs were committed to differentiate into osteoblasts in the presence of the modular peptides. HA discs functionalized with the E7 BMP-7 modular peptide showed the best capability in inducing the osteogenic differentiation of MSCs among all modular peptides studied. The modular peptides can easily be used to functionalize the HA implants through its constituent HA-binding motif, leaving the osteogenic peptide motif protruding from the surface for inducing osteogenesis. Our work opens up a new approach to the formulation of new bioactive HA coatings and implants for bone and dental repair.
机译:羟基磷灰石(HA)是骨矿物质的主要成分,当用于涂覆金属植入物以及合成骨移植物中的支架材料时,具有骨传导性能。为了使这种材料具有骨诱导能力以促进更快的骨再生,我们展示了一种简单的方法来对HA植入物表面进行功能化,并通过使用HA结合模块肽使它们具有骨诱导特性。模块化肽被设计为两个域的组合,HA结合肽基序和源自成骨生长肽(OGP)或骨形态计量蛋白7(BMP-7)的成骨肽基序。为了确定最佳的HA结合肽,比较了几种源自自然骨细胞外基质蛋白(骨唾液蛋白,骨连接蛋白,骨钙蛋白和唾液素斯坦汀)的受自然启发的肽的HA结合活性,揭示了浓度依赖性和孵育时间。依赖行为。我们发现,Poly-E七聚体(E7)是最好的HA结合肽,因此将其与第二个成骨性肽域结合在一起,从而形成了骨诱导性模块化肽。结合/释放特征后,我们发现添加第二个成骨肽域不会改变模块化肽的结合特性,只会引起其释放动力学的轻微变化。间充质干细胞(MSCs)在用模块化肽功能化的HA底物上进行培养,并研究了在基础培养基(即没有任何成骨性补充剂)中的细胞粘附,增殖和分化。基因表达数据清楚地表明,在模块肽存在下,MSC致力于分化为成骨细胞。用E7 BMP-7模块化肽功能化的HA光盘在所有研究的模块化肽中表现出诱导MSC的成骨分化的最佳能力。模块化肽可通过其组成的HA结合基序轻松用于功能化HA植入物,使成骨肽基序从表面突出以诱导成骨作用。我们的工作开辟了一种新方法,用于配制用于骨骼和牙齿修复的新型生物活性HA涂层和植入物。

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