Converting 2D Nanofiber Membranes to 3D Hierarchical Assemblies with Structural and Compositional Gradients Regulates Cell Behavior

被引:77
作者
Chen, Shixuan [1 ,2 ]
McCarthy, Alec [1 ,2 ]
John, Johnson V. [1 ,2 ]
Su, Yajuan [1 ,2 ]
Xie, Jingwei [1 ,2 ,3 ]
机构
[1] Univ Nebraska Med Ctr, Dept Surg Transplant, Omaha, NE 68198 USA
[2] Univ Nebraska Med Ctr, Mary & Dick Holland Regenerat Med Program, Omaha, NE 68198 USA
[3] Univ Nebraska, Coll Engn, Dept Mech & Mat Engn, Lincoln, NE 68588 USA
基金
美国国家卫生研究院;
关键词
3D nanofiber assemblies; composition; fiber organization; gradients; pore size; DESIGN PRINCIPLES; ENGINEERED TUMOR; SIGNAL GRADIENTS; SCAFFOLDS; MIGRATION; HYDROGELS;
D O I
10.1002/adma.202003754
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
New methods are described for converting 2D electrospun nanofiber membranes to 3D hierarchical assemblies with structural and compositional gradients. Pore-size gradients are generated by tuning the expansion of 2D membranes in different layers with incorporation of various amounts of a surfactant during the gas-foaming process. The gradient in fiber organizations is formed by expanding 2D nanofiber membranes composed of multiple regions collected by varying rotating speeds of mandrel. A compositional gradient on 3D assemblies consisting of radially aligned nanofibers is prepared by dripping, diffusion, and crosslinking. Bone mesenchymal stem cells (BMSCs) on the 3D nanofiber assemblies with smaller pore size show significantly higher expression of hypoxia-related markers and enhanced chondrogenic differentiation compared to BMSCs cultured on the assemblies with larger pore size. The basic fibroblast growth factor gradient can accelerate fibroblast migration from the surrounding area to the center in an in vitro wound healing model. Taken together, 3D nanofiber assemblies with gradients in pore sizes, fiber organizations, and contents of signaling molecules can be used to engineer tissue constructs for tissue repair and build biomimetic disease models for studying disease biology and screening drugs, in particular, for interface tissue engineering and modeling.
引用
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页数:10
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