期刊
MATERIALS SCIENCE & ENGINEERING C-MATERIALS FOR BIOLOGICAL APPLICATIONS
卷 59, 期 -, 页码 193-202出版社
ELSEVIER SCIENCE BV
DOI: 10.1016/j.msec.2015.10.017
关键词
Tissue engineering; Mesenchymal stem cells; Three-dimensional porous scaffolds; Surface chemistry; Pore size
资金
- National Special Fund for State Key Laboratory of Bioreactor Engineering [2060204]
- Basic Research Project of Shanghai Science and Technology Commission [12JC1403101, 15JC1401402]
- National Natural Science Foundation of China [31000424, 31170951]
Biomaterial properties play significant roles in controlling cellular behaviors. The objective of the present study was to investigate how pore size and surface chemistry of three-dimensional (3D) porous scaffolds regulate the fate of mesenchymal stem cells (MSCs) in vitro in combination. First, on poly(epsilon-caprolactone) (PCL) films, the hydrolytic treatment was found to stimulate the adhesion, spreading and proliferation of human MSCs (hMSCs) in comparison with pristine films, while the aminolysis showed mixed effects. Then, 3D porous PCL scaffolds with varying pore sizes (100-200 mu m, 200-300 mu m and 300-450 mu m) were fabricated and subjected to either hydrolysis or aminolysis. It was found that a pore size of 200-300 mu m with hydrolysis in 3D scaffolds was the most favorable condition for growth of hMSCs. Importantly, while a pore size of 200-300 mu m with hydrolysis for 1 h supported the best osteogenic differentiation of hMSCs, the chondrogenic differentiation was greatest in scaffolds with a pore size of 300-450 mu m and treated with aminolysis for 1 h. Taken together, these results suggest that surface chemistry and pore size of 3D porous scaffolds may potentially have a synergistic impact on the behaviors of MSCs. (C) 2015 Elsevier B.V. All rights reserved.
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