Injectable Porous Microspheres for Articular Cartilage Regeneration through In Situ Stem Cell Recruitment and Macrophage Polarization

间充质干细胞 材料科学 再生(生物学) 软骨发生 关节软骨 透明质酸 干细胞 生物医学工程 软骨 关节软骨修复 巨噬细胞极化 炎症 组织工程 癌症研究 巨噬细胞 免疫学 细胞生物学 骨关节炎 解剖 医学 生物 体外 病理 化学 生物化学 替代医学
作者
Lang Bai,Xiaoyu Zhang,Zeyu Han,Xing Yang,Yuefeng Hao
出处
期刊:Acta Biomaterialia [Elsevier BV]
卷期号:185: 429-440
标识
DOI:10.1016/j.actbio.2024.07.007
摘要

In situ mesenchymal stem cells (MSCs) regenerative therapy holds promising potential for treating osteoarthritis. However, MSCs engraftment and intra-articular inflammation limit the therapeutic efficacy of this approach. This study introduces porous microspheres (PMs) composed of aldehyde-modified poly(lactic-co-glycolic acid), that encapsulate platelet derived growth factor-AB and kartogenin. Metformin (Met) is also incorporated onto the microsphere through a Schiff base reaction to create PMs@Met. In vitro, in vivo and ex experiments revealed that PMs@Met can be injected into the joint cavity, effectively recruiting endogenous MSCs in situ. This approach creates a favorable environment for MSCs proliferation. It also controls the intra-articular inflammatory environment by modulating the polarization of synovial macrophages, ultimately promoting cartilage repair. In summary, our study presents an innovative tissue engineering strategy for the treatment of osteoarthritis-induced articular cartilage injuries. STATEMENT OF SIGNIFICANCE: Cell therapy using autologous mesenchymal stem cells (MSCs) has potential to slow the progression of osteoarthritis (OA). Nonetheless, there are some disadvantages to adopting in situ MSCs therapy, including difficulties with MSC engraftment into cartilage-deficient regions, the effect of intra-articular inflammation on MSC therapeutic efficacy, and attaining selective chondrogenic MSC differentiation. We created injectable PLGA microspheres (PMs) that were loaded with PDGF-AB and KGN. Metformin was bonded to the surface of microspheres using a Schiff base reaction. The microspheres can recruit intra-articular MSCs and encourage their development into chondrocytes. The microspheres actively modulate the inflammatory joint environment by altering synovial macrophage polarization, thereby supporting MSCs in effective cartilage treatment. To summarize, microspheres hold great potential in the treatment of OA.
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