木质素复合材料持续清除ROS和细胞外氧合,改善糖尿病伤口新生血管和愈合

Jangwook P Jung, Oluyinka O Olutoye, Tanuj J Prajati, Olivia S Jung, Lane D Yutzy, Kenny L Nguyen, Stephen W Wheat, JoAnne Huang, Benjamin W Padon, Fayiz Faruk, Sonya S Keswani, Phillip Kogan, Aditya Kaul, Ling Yu, Hui Li, Shiyanth Thevasagayampillai, Mary E Guerra, Walker D Short, Preethi H Gunaratne, Swathi Balaji
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引用次数: 0

摘要

虽然伤口愈合延迟是糖尿病患者重要的临床并发症,但目前针对糖尿病患者的治疗方法很少,促进糖尿病伤口愈合仍然是一个挑战。新生血管受损是糖尿病型伤口延迟愈合的主要特征之一。此外,活性氧(ROS)水平升高和慢性低度炎症和缺氧与糖尿病有关,这会破坏伤口愈合机制。我们开发了具有几种伤口愈合特性的木质素磺酸复合材料,包括通过过氧化钙纳米颗粒和活性氧持续释放氧气,以及硫代木质素磺酸纳米颗粒清除自由基。在体外高糖条件下,这些复合材料持续释放氧气和清除ros促进内皮细胞(EC)分支和特征性毛细血管样网络的形成。木质素复合材料培养的内皮细胞rna测序结果的基因共表达网络分析显示,除了调节血管生成缺氧诱导因子-1α (HIF-1α)和血管内皮生长因子(VEGF)途径外,还调节炎症途径。在体内,木质素磺酸复合处理促进了糖尿病小鼠全层皮肤创面中VEGF的表达和血管生成,这是一种延迟创面愈合的模型。用木质素磺酸复合材料治疗糖尿病创面也促进了损伤后第7天上皮间隙的更快闭合和肉芽组织沉积的增加,促愈合型巨噬细胞的存在增加。我们的研究结果表明木质素磺酸盐复合材料促进糖尿病伤口愈合而不需要额外的药物。这突出了功能化木质素磺酸盐在需要平衡抗氧化和控制氧气释放的伤口愈合应用中的潜力。意义声明:本研究中开发的木质素磺酸盐复合材料为糖尿病患者伤口延迟愈合提供了一个有希望的解决方案。通过有效地解决导致糖尿病伤口多方面病理生理的关键因素,包括新生血管受损、ROS水平升高、慢性炎症和伤口蛋白水解,这些复合材料显示出促进伤口修复和减少糖尿病伤口相关并发症的巨大潜力。这些木质素磺酸基材料具有促血管生成、氧释放、ECM重塑和抗氧化特性的独特组合,突出了它们作为一种有价值的治疗选择的潜力,为糖尿病伤口愈合提供了一种多管齐下的方法,而无需额外的药物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Sustained ROS Scavenging and Pericellular Oxygenation by Lignin Composites Rescue HIF-1α and VEGF Levels to Improve Diabetic Wound Neovascularization and Healing.

Although delayed wound healing is an important clinical complication in diabetic patients, few targeted treatments are available, and it remains a challenge to promote diabetic wound healing. Impaired neovascularization is one of the prime characteristics of the diabetic phenotype of delayed wound healing. Additionally, increased levels of reactive oxygen species (ROS) and chronic low-grade inflammation and hypoxia are associated with diabetes, which disrupts mechanisms of wound healing. We developed lignosulfonate composites with several wound healing properties, including sustained oxygen release through calcium peroxide nanoparticles and reactive oxygen species and free radical scavenging by thiolated lignosulfonate nanoparticles. Sustained release of oxygen and ROS-scavenging by these composites promoted endothelial cell (EC) branching and characteristic capillary-like network formation under high glucose conditions in vitro. Gene co-expression network analysis of RNA-sequencing results from ECs cultured on lignin composites showed regulation of inflammatory pathways, alongside the regulation of angiogenic hypoxia-inducible factor-1α (HIF-1α) and vascular endothelial growth (VEGF) factor pathways. In vivo, lignosulfonate composite treatment promoted VEGF expression and angiogenesis in full thickness skin wounds in diabetic mice, a model of delayed wound healing. Treatment of diabetic wounds with lignosulfonate composites also promoted faster epithelial gap closure and increased granulation tissue deposition by day 7 post-wounding, with a higher presence of pro-healing type macrophages. Our findings demonstrate that lignosulfonate composites promote diabetic wound healing without requiring additional drugs. This highlights the potential of functionalized lignosulfonate for wound healing applications that require balanced antioxidation and controlled oxygen release. STATEMENT OF SIGNIFICANCE: The lignosulfonate composites developed in this study offer a promising solution for delayed wound healing in diabetic patients. By effectively addressing key factors contributing to the multifaceted pathophysiology of the diabetic wounds, including impaired neovascularization, increased ROS levels, and chronic inflammation and wound proteolysis, these composites demonstrate significant potential for promoting wound repair and reducing the complications associated with diabetic wounds. The unique combination of pro-angiogenic, oxygen-releasing, ECM remodeling and antioxidant properties in these lignosulfonate-based materials highlights their potential as a valuable therapeutic option, providing a multi-pronged approach to diabetic wound healing without the need for additional drugs.

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