Stem Cells Expansion Vector via Bioadhesive Porous Microspheres for Accelerating Articular Cartilage Regeneration

Author:

Bai Lang12,Han Qibin12,Han Zeyu3,Zhang Xiaoyu12,Zhao Jingwen3,Ruan Huitong3,Wang Junliang4,Lin Feng4,Cui Wenguo3ORCID,Yang Xing12,Hao Yuefeng12

Affiliation:

1. Department of orthopedics Affiliated Suzhou Hospital of Nanjing Medical University Suzhou Jiangsu 215008 China

2. Gusu School Nanjing Medical University 458 Shizi Road Suzhou 215006 P. R. China

3. Department of Orthopaedics Shanghai Key Laboratory for Prevention and Treatment of Bone and Joint Diseases Shanghai Institute of Traumatology and Orthopaedics Ruijin Hospital Shanghai Jiao Tong University School of Medicine 197 Ruijin 2nd Road Shanghai 200025 P. R. China

4. Department of Orthopedic Surgery Hainan Hospital of Chinese People's Liberation Army General Hospital Sanya 572022 China

Abstract

AbstractStem 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 × 104 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.

Funder

Shanghai Municipal Health Commission

Publisher

Wiley

Subject

Pharmaceutical Science,Biomedical Engineering,Biomaterials

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