间充质干细胞
PLGA公司
干细胞
生物医学工程
材料科学
组织工程
再生(生物学)
骨关节炎
细胞
化学
细胞生物学
生物物理学
体外
医学
病理
生物
生物化学
替代医学
作者
Lang Bai,Qibin Han,Zeyu Han,Xiaoyu Zhang,Jingwen Zhao,Huitong Ruan,Junliang Wang,Feng Lin,Wenguo Cui,Xing Yang,Yuefeng Hao
标识
DOI:10.1002/adhm.202302327
摘要
Abstract Stem cell tissue engineering is a potential treatment for osteoarthritis. However, the number of stem cells that can be delivered, loss of stem cells during injection, and migration ability of stem cells limit applications of traditional stem cell tissue engineering. Herein, kartogenin (KGN)‐loaded poly(lactic ‐co‐ glycolic acid) (PLGA) porous microspheres is first engineered via emulsification, and then anchored with chitosan through the amidation reaction to develop a new porous microsphere (PLGA‐CS@KGN) as a stem cell expansion vector. Following 3D co‐culture of the PLGA‐CS@KGN carrier with mesenchymal stem cells (MSCs), the delivery system is injected into the capsule cavity in situ. In vivo and in vitro experiments show that PLGA‐CS microspheres have a high cell‐carrying capacity up to 1 × 10 4 mm −3 and provide effective protection of MSCs to promote their controlled release in the osteoarthritis microenvironment. Simultaneously, KGN loaded inside the microspheres effectively cooperated with PLGA‐CS to induce MSCs to differentiate into chondrocytes. Overall, these findings indicate that PLGA‐CS@KGN microspheres held high cell‐loading ability, adapt to the migration and expansion of cells, and promote MSCs to express markers associated with cartilage repair. Thus, PLGA‐CS@KGN can be used as a potential stem cell carrier for enhancing stem cell therapy in osteoarthritis treatment.
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