一种增加与伤口愈合相关的细胞代谢活性和迁移反应的“甜蜜”方式:脱氧糖掺入聚合物纤维作为生物活性伤口贴片。

Serkan Dikici
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引用次数: 1

摘要

伤口敷料的选择是成功处理伤口的关键。对于简单伤口的治疗,传统敷料是可取的。然而,当涉及到治疗非自愈伤口时,需要一种支持伤口管理和加速愈合过程的生物活性伤口敷料。2-脱氧-d -核糖(2dDR)是一种天然存在于人体内的小脱氧糖。虽然我们之前已经证明2dDR可以用于诱导体外和体内的新生血管和加速伤口愈合,但关于小糖的文献是相互矛盾的,关于2dDR如何实现其生物活性的知识非常有限。在这项研究中,通过研究几种小糖,包括d -葡萄糖(DG)、2-脱氧-d -葡萄糖(2dDG)、2-脱氧- l -核糖(2dLR)对人真皮微血管内皮细胞(HDMECs)和人真皮成纤维细胞(HDFs)代谢活性的影响,将它们与2dDR进行了比较。然后,首次使用二维(2D)划伤愈合模型来探索HDFs对2dDR治疗的迁移反应。最后,通过静电纺丝将2dDR掺入聚(3-羟基丁酸-co-3-羟戊酸)(PHBV)聚合物纤维中,并通过Alamar Blue法研究两种类型细胞的体外代谢活性对糖释放的响应。结果表明,在2D划痕实验中,2dDR是唯一一种糖,在其他糖中,它可以增强hdmes和HDFs的代谢活性,并以剂量依赖的方式增强HDFs的迁移反应。除了直接给药外,研究还发现,从聚合物纤维中释放后,2dDR在7天内可增加hdmec和HDFs的代谢活性。综上所述,2dDR是一种潜在的促血管生成药物,不仅对内皮细胞有积极的影响,而且对成纤维细胞也有积极的影响,在伤口愈合中起关键作用。它可以很容易地引入聚合物支架并快速释放,以增强与血管生成和伤口愈合相关的细胞的代谢活性和迁移反应。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

A "sweet" way to increase the metabolic activity and migratory response of cells associated with wound healing: deoxy-sugar incorporated polymer fibres as a bioactive wound patch.

A "sweet" way to increase the metabolic activity and migratory response of cells associated with wound healing: deoxy-sugar incorporated polymer fibres as a bioactive wound patch.

A "sweet" way to increase the metabolic activity and migratory response of cells associated with wound healing: deoxy-sugar incorporated polymer fibres as a bioactive wound patch.

A "sweet" way to increase the metabolic activity and migratory response of cells associated with wound healing: deoxy-sugar incorporated polymer fibres as a bioactive wound patch.

The selection of a wound dressing is crucial for successful wound management. Conventional dressings are preferable for the treatment of simple wounds. However, a bioactive wound dressing that supports wound management and accelerates the healing process is required when it comes to treating non-self-healing wounds. 2-deoxy-D-ribose (2dDR) is a small deoxy sugar that naturally occurs in human body. Although we have previously demonstrated that 2dDR can be used to induce neovascularisation and accelerates wound healing in vitro and in vivo, the literature on small sugars is conflicting, and the knowledge on how 2dDR achieves its biological activity is very limited. In this study, several small sugars including D-glucose (DG), 2-deoxy-D-glucose (2dDG), 2deoxy-L-ribose (2dLR) were compared to 2dDR by investigating their effects on the metabolic activities of both human dermal microvascular endothelial cells (HDMECs) and human dermal fibroblasts (HDFs). Then, for the first time, a two-dimensional (2D) scratch wound healing model was used to explore the migratory response of HDFs in response to 2dDR treatment. Finally, 2dDR was incorporated into Poly(3-hydroxybutyrate-co-3-hydroxyvalerate) (PHBV) polymer fibres via electrospinning, and the metabolic activity of both types of cells in vitro was investigated in response to sugar release via Alamar Blue assay. The results demonstrated that 2dDR was the only sugar, among others, that enhances the metabolic activity of both HDMECs and HDFs and the migratory response of HDFs in a 2D scratch assay in a dose-dependent manner. In addition to direct administration, 2dDR was also found to increase the metabolic activity of HDMECs and HDFs over 7 days when released from polymer fibres. It is concluded that 2dDR is a potential pro-angiogenic agent that has a positive impact not only on endothelial cells but also fibroblasts, which take a key role in wound healing. It could easily be introduced into polymeric scaffolds to be released quickly to enhance the metabolic activity and the migratory response of cells that are associated with angiogenesis and wound healing.

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