Rui Min, Mao Jiannan, Wu Hongshuai, Hui Yujian, Shen Hao, Yang Yilin, Ma Tao, Ren Kewei, Wang Juan, Cui Wenguo, Shi Qin, Yang Huilin
Department of Orthopaedics, The First Affiliated Hospital of Soochow University, Orthopaedic Institute of Soochow University, 899 Pinghai Road, Suzhou, Jiangsu, 215031, P. R. China.
Department of Orthopaedics, Wuxi Key Laboratory of Biomaterials for Clinical Application, Department of Central Laboratory, Jiangyin Clinical College of Xuzhou Medical University, No.163 Shoushan Road, Jiangyin, Jiangsu, 214400, P. R. China.
Adv Sci (Weinh). 2025 Jan;12(3):e2409636. doi: 10.1002/advs.202409636. Epub 2024 Nov 26.
Hypoxia and reactive oxygen species (ROS) overaccumulation cause persistent oxidative stress and impair intrinsic regenerative potential upon tissue injury. For local tissue injury with hypoxia, such as bone fracture and defects, a localized-sufficient oxygen supply is highly desirable but remains challenging. Therefore, to explore a strategy and its intrinsic mechanism for supplying oxygen locally and remodeling the regenerative microenvironment, an innovative oxygenating hydrogel microsphere system with sustained oxygenation and antioxidant properties is introduced by loading CaO@SiO@PDA (CSP) nanoparticles. Specifically, the CSP nanoparticles exhibited broad-spectrum free radicals scavenging ability, along with prolonged controlled-release of oxygen once integrated into the gelatin methacrylate anhydride (GelMA) microspheres (CSP-GM). The CSP-GM with extra cellular matrix (ECM)-mimicking structures reconstructed living niches, promoting the adhesion and proliferation of bone marrow stromal cells (BMSCs). As a multifaceted microenvironment regulator, CSP-GM remodeled the regenerative microenvironment by synergistically producing oxygen and scavenging ROS, recovering mitochondrial homeostasis and antioxidant defenses of BMSCs, promoting angiogenesis and osteogenesis under hypoxia conditions via precisely modulating the Nrf2/HO-1 signaling pathway. The multiple pro-regenerative effects of the implantable functionalized micro-oxygen reservoir on bone repair are further corroborated by the enhanced vascularized bone formation in rat femoral defects, presenting a comprehensive and promising strategy for tissue repair.
缺氧和活性氧(ROS)过度积累会导致持续的氧化应激,并损害组织损伤时的内在再生潜力。对于伴有缺氧的局部组织损伤,如骨折和骨缺损,局部充足的氧气供应是非常理想的,但仍然具有挑战性。因此,为了探索一种局部供氧和重塑再生微环境的策略及其内在机制,通过负载CaO@SiO@PDA(CSP)纳米颗粒引入了一种具有持续氧合和抗氧化特性的创新型氧合水凝胶微球系统。具体而言,CSP纳米颗粒表现出广谱自由基清除能力,一旦整合到甲基丙烯酸酐明胶(GelMA)微球(CSP-GM)中,还能实现氧气的长效控释。具有细胞外基质(ECM)模拟结构的CSP-GM重建了活细胞龛,促进了骨髓基质细胞(BMSC)的黏附和增殖。作为一种多方面的微环境调节剂,CSP-GM通过协同产氧和清除ROS来重塑再生微环境,恢复BMSC的线粒体稳态和抗氧化防御能力,通过精确调节Nrf2/HO-1信号通路在缺氧条件下促进血管生成和成骨。大鼠股骨缺损处血管化骨形成增强进一步证实了这种可植入的功能化微氧储备对骨修复的多种促再生作用,为组织修复提供了一种全面且有前景的策略。