促进皮瓣存活的微环境重塑自愈合水凝胶

IF 8.1 Q1 ENGINEERING, BIOMEDICAL
Biomaterials research Pub Date : 2024-02-22 eCollection Date: 2024-01-01 DOI:10.34133/bmr.0001
Yikun Ju, Pu Yang, Xiangjun Liu, Zhihua Qiao, Naisi Shen, Lanjie Lei, Bairong Fang
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引用次数: 0

摘要

随机皮瓣移植是整形外科用于修复和重建大面积组织缺损的常规手术。皮瓣坏死的主要原因是缺血再灌注损伤和皮瓣远端供血不足。缺血再灌注损伤会导致产生过多的活性氧,形成病理微环境,损害细胞功能和血管生成。在本研究中,我们开发了一种微环境重塑自愈合水凝胶[基于层粘蛋白-壳聚糖的水凝胶-负载细胞外囊泡和铈纳米酶(LCH@EVs&CNZs)],以改善皮瓣微环境并协同促进皮瓣再生和存活。天然自愈合水凝胶(LCH)是通过席夫碱反应将层粘蛋白和羧甲基壳聚糖氧化而成的。我们在这种水凝胶中添加了 CNZs 和 EVs。CNZs 是一类具有酶活性的纳米材料,具有很强的清除活性氧的能力,从而缓解氧化应激。EVs 是细胞分泌的囊泡结构,含有数千种生物活性物质,可促进细胞增殖、迁移、分化和血管生成。所构建的 LCH@EVs&CNZs 具有强大的清除过量活性氧的能力,从而在氧化应激环境中为细胞提供保护。此外,这些构建体还能显著促进细胞迁移和血管生成。我们的研究结果表明,LCH@EVs&CNZs 能有效重塑病理皮瓣微环境,显著提高皮瓣存活率。这种方法引入了一种新的治疗策略,将微环境重塑与 EV 治疗相结合,有望促进皮瓣存活。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Microenvironment Remodeling Self-Healing Hydrogel for Promoting Flap Survival.

Random flap grafting is a routine procedure used in plastic and reconstructive surgery to repair and reconstruct large tissue defects. Flap necrosis is primarily caused by ischemia-reperfusion injury and inadequate blood supply to the distal flap. Ischemia-reperfusion injury leads to the production of excessive reactive oxygen species, creating a pathological microenvironment that impairs cellular function and angiogenesis. In this study, we developed a microenvironment remodeling self-healing hydrogel [laminarin-chitosan-based hydrogel-loaded extracellular vesicles and ceria nanozymes (LCH@EVs&CNZs)] to improve the flap microenvironment and synergistically promote flap regeneration and survival. The natural self-healing hydrogel (LCH) was created by the oxidation laminarin and carboxymethylated chitosan via a Schiff base reaction. We loaded this hydrogel with CNZs and EVs. CNZs are a class of nanomaterials with enzymatic activity known for their strong scavenging capacity for reactive oxygen species, thus alleviating oxidative stress. EVs are cell-secreted vesicular structures containing thousands of bioactive substances that can promote cell proliferation, migration, differentiation, and angiogenesis. The constructed LCH@EVs&CNZs demonstrated a robust capacity for scavenging excess reactive oxygen species, thereby conferring cellular protection in oxidative stress environments. Moreover, these constructs notably enhance cell migration and angiogenesis. Our results demonstrate that LCH@EVs&CNZs effectively remodel the pathological skin flap microenvironment and marked improve flap survival. This approach introduces a new therapeutic strategy combining microenvironmental remodeling with EV therapy, which holds promise for promoting flap survival.

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