Injectable dECM-enhanced hyaluronic microgels with spatiotemporal release of cartilage-specific molecules to improve osteoarthritic chondrocyte’s function
Siyan Deng, Hongfu Cao, Yan Lu, Wenqing Shi, Manyu Chen, Xiaolin Cui, Jie Liang, Yujiang Fan, Qiguang Wang, Xingdong Zhang
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引用次数: 0
Abstract
The interior environment of articular cartilage in osteoarthritis (OA) presents substantial hurdles, leading to the malfunction of chondrocytes and the breakdown of collagen II-enriched hyaline cartilage matrix. Despite this, most clinical treatments primarily provide temporary relief from OA discomfort without arresting OA progression. This study aimed to alleviate OA by developing intra-articular injectable dECM-enhanced hyaluronic (HE) microgels. The HE hydrogel was engineered and shaped into uniformly sized microgels using microfluidics and photopolymerization techniques. These microgels provided a spatiotemporal cascade effect, facilitating the rapid release of growth factors and a slower release of ECM macromolecules and proteins. This process assisted in the recovery of OA chondrocytes’ function, promoting cell proliferation, matrix synthesis, and cartilage-specific gene expression in vitro. It also effectively aided repair of the collagen II-enriched hyaline cartilage and significantly reduced the severity of OA, as demonstrated by radiological observation, gross appearance, histological/immunohistochemical staining, and analysis in an OA rat model in vivo. Collectively, the HE injectable microgels with spatiotemporal release of cartilage-specific molecules have shown promise as a potential candidate for a cell-free OA therapy approach.
骨关节炎(OA)的关节软骨内部环境存在巨大障碍,导致软骨细胞功能失调和富含胶原蛋白 II 的透明软骨基质分解。尽管如此,大多数临床治疗方法只能暂时缓解 OA 带来的不适,却无法阻止 OA 的发展。本研究旨在通过开发可关节内注射的 dECM 增强透明质酸(HE)微凝胶来缓解 OA。利用微流体技术和光聚合技术,将透明质酸水凝胶设计和成型为大小一致的微凝胶。这些微凝胶产生了时空级联效应,促进了生长因子的快速释放以及 ECM 大分子和蛋白质的缓慢释放。这一过程有助于恢复 OA 软骨细胞的功能,促进细胞增殖、基质合成和体外软骨特异性基因表达。在 OA 大鼠模型中进行的放射学观察、大体外观、组织学/免疫组织化学染色和体内分析表明,它还能有效帮助修复富含胶原蛋白 II 的透明软骨,并显著减轻 OA 的严重程度。总之,具有软骨特异性分子时空释放功能的 HE 可注射微凝胶有望成为无细胞 OA 治疗方法的潜在候选材料。