regulation of epithelial cell morphology and functions approaching to more in vivo-like by modifying polyethylene glycol on polysulfone membranes调节上皮细胞形态和功能接近更多vivo-like通过修改聚乙二醇聚砜膜.pdfVIP

regulation of epithelial cell morphology and functions approaching to more in vivo-like by modifying polyethylene glycol on polysulfone membranes调节上皮细胞形态和功能接近更多vivo-like通过修改聚乙二醇聚砜膜.pdf

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regulation of epithelial cell morphology and functions approaching to more in vivo-like by modifying polyethylene glycol on polysulfone membranes调节上皮细胞形态和功能接近更多vivo-like通过修改聚乙二醇聚砜膜

Regulation of Epithelial Cell Morphology and Functions Approaching To More In Vivo-Like by Modifying Polyethylene Glycol on Polysulfone Membranes 1 2 1 Chong Shen , Guoliang Zhang , Qin Meng * 1 Department of Chemical and Biological Engineering, Zhejiang University, Hangzhou, China, 2 College of Biological and Environmental Engineering, Zhejiang University of Technology, Hangzhou, China Abstract Cytocompatibility is critically important in design of biomaterials for application in tissue engineering. However, the currently well-accepted ‘‘cytocompatible’’ biomaterials are those which promote cells to sustain good attachment/ spreading. The cells on such materials usually lack the self-assembled cell morphology and high cell functions as in vivo. In our view, biomaterials that can promote the ability of cells to self-assemble and demonstrate cell-specific functions would be cytocompatible. This paper examined the interaction of polyethylene glycol (PEG) modified polysulfone (PSf) membranes with four epithelial cell types (primary liver cells, a liver tumor cell line, and two renal tubular cell lines). Our results show that PSf membranes modified with proper PEG promoted the aggregation of both liver and renal cells, but the liver cells more easily formed aggregates than the renal tubular cells. The culture on PEG-modified PSf membranes also enhanced cell- specific functions. In particular, the cells cultured on F127 membranes with the proper PEG content mimicked the in vivo ultrastructure of liver cells or renal tubules cells and displayed the highest cell functions. Gene expression data for adhesion proteins suggest that the PEG modification impaired cell-membrane interactions and increased cell-cell interactions, thus facilitating cell self-assembly. In conc

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