TGF-β3负载氧化石墨烯-自组装肽杂化水凝胶作为髓核再生的功能3D支架

C. Ligorio, Marie O'Brien, N. Hodson, Aleksandr Mironov, Maria Iliut, A. Miller, A. Vijayaraghavan, J. Hoyland, A. Saiani
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引用次数: 25

摘要

椎间盘(IVD)退变是一个始于中央髓核(NP)并导致炎症、细胞外基质(ECM)降解和椎间盘高度进行性丧失的过程。IVD退变的早期治疗对于减少腰痛和相关残疾至关重要。因此,在疾病的早期阶段,需要能够阻止和逆转NP变性的微创治疗方法。最近,我们开发了一种可注射的氧化石墨烯(GO) -自组装肽FEFKFEFK (F:苯丙氨酸;凯西:赖氨酸;E:谷氨酸)杂化水凝胶作为NP中细胞和/或药物的潜在递送平台。在当前的研究中,我们探索了使用这些混合水凝胶中的氧化石墨烯作为隔离和控制传递转化生长因子β -3 (TGF-β3)的载体的可能性,转化生长因子β -3是一种已知指导NP细胞命运和功能的合成代谢生长因子(GF)。为此,我们首先研究了氧化石墨烯结合和隔离TGF-β3的潜力。然后,我们在新的功能支架中培养牛NP细胞,并研究它们对氧化石墨烯和TGF-β3存在的反应。我们的研究结果清楚地表明,氧化石墨烯薄片可以通过强结合相互作用隔离TGF-β3,导致GF在与氧化石墨烯薄片结合后仍保持活性,释放缓慢而持久。GF吸附在氧化石墨烯薄片上,形成负载TGF-β3的氧化石墨烯薄片,并通过混合[(GO/TGF-β3Ads)-F8]水凝胶将其掺入水凝胶中,导致np特异性基因上调,同时产生和沉积富含聚集蛋白和胶原II的np样ECM。NP细胞积极与负载TGF-β3的氧化石墨烯薄片相互作用,并通过内吞作用重塑支架。这项工作强调了使用氧化石墨烯作为纳米载体设计功能杂化肽基水凝胶的潜力。意义声明:椎间盘(IVD)退变是一个始于中央髓核(NP)并导致炎症、细胞外基质(ECM)降解和椎间盘高度进行性丧失的过程。因此,在疾病的早期阶段,需要能够阻止和逆转NP变性的微创治疗方法。在当前的研究中,我们探索了使用肽-氧化石墨烯混合水凝胶作为隔离和控制传递转化生长因子β -3 (TGF-β3)的载体的可能性,转化生长因子β -3是一种已知的指导NP细胞命运和功能的合成代谢生长因子(GF)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
TGF-β3-Loaded Graphene Oxide - Self-Assembling Peptide Hybrid Hydrogels as Functional 3D Scaffolds for the Regeneration of the Nucleus Pulposus
Intervertebral disc (IVD) degeneration is a process that starts in the central nucleus pulposus (NP) and leads to inflammation, extracellular matrix (ECM) degradation, and progressive loss of disc height. Early treatment of IVD degeneration is critical to the reduction of low back pain and related disability. As such, minimally invasive therapeutic approaches that can halt and reverse NP degeneration at the early stages of the disease are needed. Recently, we developed an injectable graphene oxide (GO) - self-assembling peptide FEFKFEFK (F: phenylalanine; K: lysine; E: glutamic acid) hybrid hydrogels as potential delivery platform for cells and/or drugs in the NP. In this current study, we explored the possibility of using the GO present in these hybrid hydrogels as a vehicle for the sequestration and controlled delivery of transforming growth factor beta-3 (TGF-β3), an anabolic growth factor (GF) known to direct NP cell fate and function. For this purpose, we first investigated the potential of GO to bind and sequestrate TGF-β3. We then cultured bovine NP cells in the new functional scaffolds and investigated their response to the presence of GO and TGF-β3. Our results clearly showed that GO flakes can sequestrate TGF-β3 through strong binding interactions resulting in a slow and prolonged release with the GF remaining active even when bound to the GO flakes. The adsorption of the GF on the GO flakes to create TGF-β3-loaded GO flakes and their subsequent incorporation in the hydrogels through mixing, [(GO/TGF-β3Ads)-F8] hydrogel, led to the upregulation of NP-specific genes, accompanied by the production and deposition of an NP-like ECM, rich in aggrecan and collagen II. NP cells actively interacted with TGF-β3-loaded GO flakes and remodeled the scaffolds through endocytosis. This work highlights the potential of using GO as a nanocarrier for the design of functional hybrid peptide-based hydrogels. STATEMENT OF SIGNIFICANCE: : Intervertebral disc (IVD) degeneration is a process that starts in the central nucleus pulposus (NP) and leads to inflammation, extracellular matrix (ECM) degradation, and progressive loss of disc height. As such, minimally invasive therapeutic approaches that can halt and reverse NP degeneration at the early stages of the disease are needed. In this current study, we explored the possibility of using peptide - GO hybrid hydrogels as a vehicle for the sequestration and controlled delivery of transforming growth factor beta-3 (TGF-β3), an anabolic growth factor (GF) known to direct NP cell fate and function.
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