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Hydroxyapatite nanoparticle injectable hydrogel scaffold to support osteogenic differentiation of human mesenchymal stem cells

机译:羟基磷灰石纳米颗粒可注射水凝胶支架支持人间充质干细胞的成骨分化

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Bone loss associated with degenerative disease and trauma is a clinical problem increasing with the aging population. Thus, effective bone augmentation strategies are required; however, many have the disadvantages that they require invasive surgery and often the addition of expensive growth factors to induce osteoblast differentiation. Here, we investigated a LaponiteÒ crosslinked, pNIPAM-DMAc copolymer (L-pNIPAM-co-DMAc) hydrogel with hydroxyapatite nanoparticles (HAPna), which can be maintained as a liquid ex vivo, injected via narrow-gauge needle into affected bone, followed by in situ gelation to deliver and induce osteogenic differentiation of human mesenchymal stem cells (hMSC). L-pNIPAM-co-DMAc hydrogels were synthesised and HAPna added post polymerisation. Commercial hMSCs from one donor (Lonza) were incorporated in liquid hydrogel, the mixture solidified and cultured for up to 6 weeks. Viability of hMSCs was maintained within hydrogel constructs containing 0.5 mg/mL HAPna. SEM analysis demonstrated matrix deposition in cellular hydrogels which were absent in acellular controls. A significant increase in storage modulus (G') was observed in cellular hydrogels with 0.5 mg/mL HAPna. Semi-quantitative immunohistochemistry and histological analysis demonstrated that bone differentiation markers and collagen deposition was induced within 48 h, with increased calcium deposition with time. The thermally triggered hydrogel system, described here, was sufficient without the need of additional growth factors or osteogenic media to induce osteogenic differentiation of commercial hMSCs. Preliminary data presented here will be expanded on multiple patient samples to ensure differentiation is seen in these samples. This system could potentially reduce treatment costs and simplify the treatment strategy for orthopaedic repair and regeneration.
机译:与变性疾病和创伤相关的骨丢失是随着人口老龄化而增加的临床问题。因此,需要有效的骨骼增强策略。然而,许多缺点是需要进行侵入性手术,并且常常需要添加昂贵的生长因子来诱导成骨细胞分化。在这里,我们研究了Laponite交联的pNIPAM-DMAc共聚物(L-pNIPAM-co-DMAc)与羟基磷灰石纳米颗粒(HAPna)的水凝胶,可以将其保持为离体液体,通过窄针头注射到患骨中,通过原位凝胶传递和诱导人间充质干细胞(hMSC)的成骨分化。合成了L-pNIPAM-co-DMAc水凝胶,并在聚合后添加了HAPna。将来自一个供体(Lonza)的商业hMSC掺入液体水凝胶中,混合物固化并培养长达6周。 hMSC的活力在含有0.5 mg / mL HAPna的水凝胶构建物中得以维持。 SEM分析表明基质沉积在无细胞对照中不存在的细胞水凝胶中。在含有0.5 mg / mL HAPna的细胞水凝胶中观察到储能模量(G')显着增加。半定量免疫组织化学和组织学分析表明,在48小时内诱导了骨分化标志物和胶原蛋白沉积,钙沉积随时间增加。本文所述的热触发水凝胶系统就足够了,而无需其他生长因子或成骨培养基来诱导商用hMSC的成骨分化。此处提供的初步数据将扩展到多个患者样品上,以确保在这些样品中看到差异。该系统可以潜在地降低治疗成本,并简化骨科修复和再生的治疗策略。

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