4.5 Article

Novel temperature-responsive polymer brushes with carbohydrate residues facilitate selective adhesion and collection of hepatocytes

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出版社

TAYLOR & FRANCIS LTD
DOI: 10.1088/1468-6996/13/6/064206

关键词

poly(N-isopropylacrylamide); 2-lactobionamidoethyl methacrylate; atom transfer radical polymerization; hepatocytes; selective cell adhesion; cell detachment

资金

  1. Research Fellowships of the Japan Society for Promotion of Science (JSPS) for Young Scientists
  2. Japan Society for the Promotion of Science (JSPS) through the 'Funding Program for World-Leading Innovative R&D on Science and Technology (FIRST Program)'
  3. Grants-in-Aid for Scientific Research [23650295, 22680042, 10J04375] Funding Source: KAKEN

向作者/读者索取更多资源

Temperature-responsive glycopolymer brushes were designed to investigate the effects of grafting architectures of the copolymers on the selective adhesion and collection of hypatocytes. Homo, random and block sequences of N-isopropylacrylamide and 2-lactobionamidoethyl methacrylate were grafted on glass substrates via surface-initiated atom transfer radical polymerization. The galactose/lactose-specific lectin RCA(120) and HepG2 cells were used to test for specific recognition of the polymer brushes containing galactose residues over the lower critical solution temperatures (LCSTs). RCA(120) showed a specific binding to the brush surfaces at 37 degrees C. These brush surfaces also facilitated the adhesion of HepG2 cells at 37 degrees C under nonserum conditions, whereas no adhesion was observed for NIH-3T3 fibroblasts. When the temperature was decreased to 25 degrees C, almost all the HepG2 cells detached from the block copolymer brush, whereas the random copolymer brush did not release the cells. The difference in releasing kinetics of cells from the surfaces with different grafting architectures can be explained by the correlated effects of significant changes in LCST, mobility, hydrophilicity and mechanical properties of the grafted polymer chains. These findings are important for designing 'on-off' cell capture/release substrates for various biomedical applications such as selective cell separation.

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