Improving Functional Muscle Regeneration in Volumetric Muscle Loss Injuries by Shifting the Balance of Inflammatory and Pro-Resolving Lipid Mediators

Thomas C Turner, Frank S Pittman, Hongmanlin Zhang, Lauren A Hymel, Tianyi Zheng, Monica Behara, Shannon E Anderson, Julia Andraca Harrer, Kaitlyn A Link, Mashoor Al Ahammed, Kristal Maner-Smith, Xueyun Liu, Xuanzhi Yin, Hong Seo Lim, Matthew Spite, Peng Qiu, Andres J Garcia, Luke J. Mortensen, Young C Jang, Nick J Willett, Edward A Botchwey
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Abstract

Severe tissue loss resulting from extremity trauma, such as volumetric muscle loss (VML), poses significant clinical challenges for both general and military populations. VML disrupts the endogenous tissue repair mechanisms, resulting in acute and unresolved chronic inflammation and immune cell presence, impaired muscle healing, scar tissue formation, persistent pain, and permanent functional deficits. The aberrant healing response is preceded by acute inflammation and immune cell infiltration which does not resolve. We analyzed the biosynthesis of inflammatory and specialized pro-resolving lipid mediators (SPMs) after VML injury in two different models; muscle with critical-sized defects had a decreased capacity to biosynthesize SPMs, leading to dysregulated and persistent inflammation. We developed a modular poly(ethylene glycol)-maleimide hydrogel platform to locally release a stable isomer of Resolvin D1 (AT-RvD1) and promote endogenous pathways of inflammation resolution in the two muscle models. The local delivery of AT-RvD1 enhanced muscle regeneration, improved muscle function, and reduced pain sensitivity after VML by promoting molecular and cellular resolution of inflammation. These findings provide new insights into the pathogenesis of VML and establish a pro-resolving hydrogel therapeutic as a promising strategy for promoting functional muscle regeneration after traumatic injury.
通过改变炎症和促溶解脂质介质的平衡来改善体积性肌肉缺失损伤中的功能性肌肉再生
四肢创伤导致的严重组织损失,如肌肉体积损失(VML),给普通人群和军人带来了重大的临床挑战。体积性肌肉萎缩破坏了内源性组织修复机制,导致急性和未解决的慢性炎症和免疫细胞存在、肌肉愈合受损、瘢痕组织形成、持续疼痛和永久性功能障碍。在出现异常愈合反应之前,会出现急性炎症和免疫细胞浸润,而且这种炎症和免疫细胞浸润不会消失。我们在两种不同的模型中分析了 VML 损伤后炎症和特异性促溶解脂质介质(SPMs)的生物合成情况;临界大小缺陷的肌肉生物合成 SPMs 的能力下降,导致了失调和持续性炎症。我们开发了一种模块化聚(乙二醇)-马来酰亚胺水凝胶平台,用于在两种肌肉模型中局部释放稳定的瑞舒文 D1 异构体(AT-RvD1)并促进内源性炎症消退途径。AT-RvD1 的局部给药通过促进分子和细胞炎症的消退,增强了肌肉再生,改善了肌肉功能,并降低了 VML 后的疼痛敏感性。这些发现为了解 VML 的发病机制提供了新的视角,并将促进炎症消退的水凝胶疗法作为促进创伤后肌肉功能再生的一种有前途的策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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