Liang Feng, Zheng Yixin, Zhao Chenchen, Li Lele, Hu Yunqi, Wang Chenfeng, Wang Ruoxi, Feng Ting, Liu Xiaoyang, Cui Jiarong, Zhong Danni, Zhou Min
Department of Orthopaedics, The First Affiliated Hospital of Zhejiang University School of Medicine, Hangzhou 310000, China.
Zhejiang University-University of Edinburgh Institute (ZJU-UoE Institute), Zhejiang University School of Medicine, Zhejiang University, Haining 314400, China.
ACS Nano. 2025 Mar 4;19(8):8040-8057. doi: 10.1021/acsnano.4c16085. Epub 2025 Feb 21.
Treatment of osteoarthritis (OA) remains challenging owing to its complex pathological microenvironment, which involves reactive oxygen species, chronic inflammation, mitochondrial dysfunction, energy deficiency, and cartilage degeneration. Herein, we report for extracellular vesicles (SP-EVs) derived from the photosynthetic microorganism contain antioxidative and ATP-dependent active and metabolic-related compounds for OA treatment. SP-EVs were effectively delivered to chondrocytes, demonstrating the potential for modulating cellular communication and energy homeostasis. To facilitate sustained delivery of SP-EVs, the rhein hydrogel system was used for intra-articular injection (Rh Gel@SP-EVs), which demonstrated pH responsiveness under mildly acidic conditions and synergistic anti-inflammatory effects. Rh Gel@SP-EVs significantly rescued mitochondrial dysfunction by ameliorating inflammation-mediated oxidative stress and restoring the mitochondrial membrane potential in chondrocytes. Improved mitochondrial function facilitates the replenishment of ATP levels, further contributing to the balance of anabolic and catabolic processes within the cartilage matrix, eventually decelerating OA progression. Rh Gel@SP-EVs also modulated the Janus kinase-signal transducer and activator of transcription 3 signaling pathway, implicated in suppressing inflammatory responses. This therapeutic strategy utilized a microalgae-based herbal hydrogel system to modulate the sustained release of SP-EVs, offering an effective approach for treating OA by regulating energy metabolism and anti-inflammatory mechanisms.
骨关节炎(OA)的治疗仍然具有挑战性,因为其病理微环境复杂,涉及活性氧、慢性炎症、线粒体功能障碍、能量缺乏和软骨退变。在此,我们报道了源自光合微生物的细胞外囊泡(SP-EVs)含有用于OA治疗的抗氧化和ATP依赖性活性及代谢相关化合物。SP-EVs能有效递送至软骨细胞,显示出调节细胞通讯和能量稳态的潜力。为促进SP-EVs的持续递送,使用大黄酸水凝胶系统进行关节内注射(Rh Gel@SP-EVs),其在轻度酸性条件下表现出pH响应性和协同抗炎作用。Rh Gel@SP-EVs通过改善炎症介导的氧化应激和恢复软骨细胞中的线粒体膜电位,显著挽救了线粒体功能障碍。线粒体功能的改善有助于补充ATP水平,进一步促进软骨基质中合成代谢和分解代谢过程的平衡,最终减缓OA进展。Rh Gel@SP-EVs还调节了与抑制炎症反应有关的Janus激酶-信号转导子和转录激活子3信号通路。这种治疗策略利用基于微藻的草药水凝胶系统来调节SP-EVs的持续释放,为通过调节能量代谢和抗炎机制治疗OA提供了一种有效方法。