体外评价人肌腱源性基质细胞对新型电纺丝肌腱修复缝线的反应。

IF 1.2 Q3 SPORT SCIENCES
Andrey Nezhentsev, Roxanna E Abhari, Mathew J Baldwin, Jolet Y Mimpen, Edyta Augustyniak, Mark Isaacs, Pierre-Alexis Mouthuy, Andrew J Carr, Sarah J B Snelling
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引用次数: 7

摘要

肌腱修复手术后复发性撕裂仍然很常见。修复失败可部分归因于使用的缝合线不是为肌腱细胞生态位设计的,也不是为了促进修复过程。合成静电纺丝材料可以机械地支撑肌腱,同时提供调节细胞行为的地形线索。本文将一种由扭曲聚二氧环酮(PDO)聚合物细丝制成的新型电纺丝缝合线与PDS II进行比较,PDS II是目前用于肌腱修复的临床使用的PDO缝合线。我们使用PrestoBlue和扫描电镜评估了这些缝合线支持人肌腱源性基质细胞附着和增殖的能力。用x射线光电子能谱分析缝合线表面化学性质。Bulk RNA-Seq询问了14天后原代肌腱源性基质细胞对缝合线的转录反应。与PDS II相比,电纺丝缝合显示出初始细胞附着增加和更强的转录反应,包括mTorc1信号通路的相对富集和上皮间质转化的缺失。与基线相比,两组缝合均未诱导炎症通路的转录上调。因此,通过增加细胞附着,同时保持适当的组织反应,扭曲电纺线在外科肌腱修复中显示出改善结果的希望。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
In vitro evaluation of the response of human tendon-derived stromal cells to a novel electrospun suture for tendon repair.

Recurrent tears after surgical tendon repair remain common. Repair failures can be partly attributed to the use of sutures not designed for the tendon cellular niche nor for the promotion of repair processes. Synthetic electrospun materials can mechanically support the tendon whilst providing topographical cues that regulate cell behaviour. Here, a novel electrospun suture made from twisted polydioxanone (PDO) polymer filaments is compared to PDS II, a clinically-used PDO suture currently utilised in tendon repair. We evaluated the ability of these sutures to support the attachment and proliferation of human tendon-derived stromal cells using PrestoBlue and Scanning Electron Microscopy. Suture surface chemistry was analysed using X-ray Photoelectron Spectroscopy. Bulk RNA-Seq interrogated the transcriptional response of primary tendon-derived stromal cells to sutures after 14 days. Electrospun suture showed increased initial cell attachment and a stronger transcriptional response compared to PDS II, with relative enrichment of pathways including mTorc1 signalling and depletion of epithelial mesenchymal transition. Neither suture induced transcriptional upregulation of inflammatory pathways compared to baseline. Twisted electrospun sutures therefore show promise in improving outcomes in surgical tendon repair by allowing increased cell attachment whilst maintaining an appropriate tissue response.

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