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

炎症 再生(生物学) 肌肉组织 内生 发病机制 免疫系统 医学 病理 细胞生物学 内科学 免疫学 生物
作者
T. 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,Andrés J. Garcı́a,Luke J. Mortensen,Young C. Jang,Nick J. Willett,Edward A. Botchwey
标识
DOI:10.1101/2024.09.06.611741
摘要

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.

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