Chinese Journal of Tissue Engineering Research ›› 2020, Vol. 24 ›› Issue (28): 4540-4546.doi: 10.3969/j.issn.2095-4344.2296

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Regulation of stem cells by transforming growth factor β3/polylactic acid-glycolic acid microspheres

Yang Zhen1,2, Li Hao1,2, Gao Cangjian1,2, Fu Liwei1,2, Tian Guangzhao1,2, Zha Kangkang1,2, Sun Zhiqiang1,2, Li Xu2, Guo Weimin2, Sui Xiang2, Huang Jingxiang2, Liu Shuyun2, Lu Shibi2, Guo Quanyi2    

  1. 1Medical College of Nankai University, Tianjin 300071, China; 2Institute of Orthopedics, Chinese PLA General Hospital, Beijing Key Laboratory of Regenerative Medicine in Orthopedics, Key Laboratory of Musculoskeletal Trauma & War Injuries, PLA, Beijing 100853, China

  • Received:2019-11-12 Revised:2019-11-16 Accepted:2019-12-20 Online:2020-10-08 Published:2020-09-01
  • Contact: Guo Quanyi, Professor, Institute of Orthopedics, Chinese PLA General Hospital, Beijing Key Laboratory of Regenerative Medicine in Orthopedics, Key Laboratory of Musculoskeletal Trauma & War Injuries, PLA, Beijing 100853, China
  • About author:Yang Zhen, Master candidate, Medical College of Nankai University, Tianjin 300071, China; Institute of Orthopedics, Chinese PLA General Hospital, Beijing Key Laboratory of Regenerative Medicine in Orthopedics, Key Laboratory of Musculoskeletal Trauma & War Injuries, PLA, Beijing 100853, China
  • Supported by:
    the National Key Research and Development Plan Project, No. 2019YFA0110600; the National Natural Science Foundation of China, No. 81772319 

Abstract:

BACKGROUND: Transforming growth factor β3/polylactic acid-glycolic acid (TGF-β3/PLGA) sustained-release microspheres can maintain the effective drug concentration at the site of action and provide the feasibility for efficient utilization of growth factors.

OBJECTIVE: To optimize the manufacturing process of TGF-β3/PLGA sustained-release microspheres, and investigate their effects on the proliferation and migration of rabbit adipose-derived mesenchymal stem cells (ADSCs).

METHODS: TGF-β3/PLGA sustained-release microspheres were prepared by emulsification-solvent evaporation method. The morphology, particle size, drug spatial distribution, encapsulation efficiency, drug loading, and sustained release properties of the microspheres were characterized. The TGF-β3/PLGA sustained-release microspheres were dissolved in phosphate buffered saline. The concentration of TGF-β3 in the supernatant was detected at the corresponding time points. The microsphere morphology was observed by scanning electron microscopy at the corresponding time point. Adipose-derived mesenchymal stem cells were divided into six groups and then cultured with single culture medium (negative control) or culture medium containing TGF-β3 or blank PLGA, or culture medium containing 10,100,1 000 g/L TGF-β3/PLGA microspheres. Cell proliferation was detected by CCK-8 assay at the corresponding time point. Cells in each group were cultured for 24 hours with corresponding medium in a non-contact manner. The number of migratory cells was counted.

RESULTS AND CONCLUSION: (1) TGF-β3/PLGA sustained-release microspheres were spherical with smooth surface, no adhesion, and evenly distributed particle size. The microspheres had a diameter of 2-50 μm, and the protein drugs in the microspheres were evenly distributed, with high encapsulation efficacy and encapsulation dose. (2) The TGF-β3/PLGA sustained-release microspheres had good degradation properties and were completely degraded after 6 months in vitro. At the same time, these microspheres had good sustained-release performance and released TGF-β3 slowly for 45 days in vitro. (3) Blank microspheres and the sustained-release microspheres containing TGF-β3 had no effect on the proliferation of adipose-derived mesenchymal stem cells. (4) Blank microspheres had no effect on the migration of adipose-derived mesenchymal stem cells, and the transforming growth factor 3 and the sustained-release microspheres containing TGF-β3 promoted the migration of adipose-derived mesenchymal stem cells. There was no significant difference in the migration promotion between different concentrations of TGF-β3. (5) These findings suggest that the TGF-β3/PLGA sustained-release microspheres can promote the migration of adipose-derived mesenchymal stem cells without affecting their proliferation.

Key words: transforming growth factor beta 3, polylactic acid-glycolic acid, sustained-release microspheres, rabbit adipose-derived mesenchymal stem cells, proliferation, migration, cartilage injury, tissue engineering

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