Modulating in vitro bone cell and macrophage behavior by immobilized enzymatically tailored pectins

被引:30
作者
Bussy, Cyrill [1 ]
Verhoef, Rene [2 ]
Haeger, Ash [3 ]
Morra, Marco [4 ]
Duval, Jean-Luc [1 ]
Vigneron, Pascale [1 ]
Bensoussan, Anne [1 ]
Velzenberger, Elodie [1 ]
Cascardo, Giovanna [4 ]
Cassinelli, Clara [4 ]
Schols, Henk [2 ]
Knox, J. Paul [3 ]
Nagel, Marie-Danielle [1 ]
机构
[1] Univ Technol Compiegne, CNRS, UMR 6600, F-60206 Compiegne, France
[2] Wageningen Univ, Agrotechnol & Food Sci Grp, Food Chem Lab, NL-6703 HD Wageningen, Netherlands
[3] Univ Leeds, Ctr Plant Sci, Leeds LS2 9JT, W Yorkshire, England
[4] Nobil Bio Ric, Villafranca Asti, Italy
关键词
biomimetic surfaces; rhamnogalacturonan-I; cell-surface interaction; biocompatibility; biomaterials;
D O I
10.1002/jbm.a.31729
中图分类号
R318 [生物医学工程];
学科分类号
0831 [生物医学工程];
摘要
Previous work has reported the results of a multidisciplinary effort producing a proof-of-concept on the use of pectic polysaccharides in the surface modification of medical devices. This study was designed to learn more about the capability of engineered rhamnogalacturonan-I (RG-I) fractions of apple pectin to control bone cell and macrophage behavior. Thermanox (R) or polystyrene Petri dishes were surface modified with two different modified hairy regions (MHRs) obtained by different enzymatic liquefaction processes of apples differing in relative amounts and lengths of their neutral side chains: (long-haired) MHR-alpha and (short-haired) MHR-B. Bone explants from 14-day-old chick embryos were cultured for 14 days on both pectic substrata. MHR-B promoted cell migration and differentiation, MHR-a did not. On MHR-alpha, J774.2 macrophages grew well, their percentage in G1 phase was decreased and in S phase increased, and they did not secrete either proinflammatory-cytokines or nitrites. Contrasting results were gained from macrophages on MHR-B, except for nitrite secretion. Thus, we conclude that coatings from tailored pectins show different biological activities in vitro and are potential innovative candidates for improving the biocompatibility of medical devices in various applications. (c) 2007 Wiley Periodicals, Inc.
引用
收藏
页码:597 / 606
页数:10
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