Cell specific ingrowth hydrogels

被引:37
作者
Bracher, Mona [1 ]
Bezuidenhout, Deon [1 ]
Lutolf, Matthias P. [2 ,3 ]
Franz, Thomas [1 ,4 ,5 ]
Sun, Michelle [1 ]
Zilla, Peter [1 ]
Davies, Neil H. [1 ]
机构
[1] Univ Cape Town, Dept Hlth Sci, Cardiovasc Res Unit, Chris Barnard Div Cardiothorac Surg, ZA-7925 Cape Town, South Africa
[2] Ecole Polytech Fed Lausanne, Inst Bioengn, LSCB, Lausanne, Switzerland
[3] Ecole Polytech Fed Lausanne, Sch Life Sci, Lausanne, Switzerland
[4] Univ Cape Town, Res Off, PERC, ZA-7701 Mowbray, South Africa
[5] Univ Cape Town, Ctr Res Computat & Appl Mech, ZA-7701 Rondebosch, South Africa
基金
英国医学研究理事会;
关键词
Biomimetic material; Hydrogel; Fibroblast; Matrix metalloproteinase; Smooth muscle cell; MATRIX-METALLOPROTEINASE EXPRESSION; ENGINEERED PEG HYDROGELS; MICHAEL-TYPE ADDITION; EXTRACELLULAR MATRICES; DEGRADATION; MATRIX-METALLOPROTEINASE-9; IDENTIFICATION; MIGRATION; LIBRARIES; DISPLAY;
D O I
10.1016/j.biomaterials.2013.05.057
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Extracellular mimetic hydrogels formed from peptide crosslinkers and polyethylene glycol monomers permit cell-controlled invasion. The use of matrix metalloproteinase specific peptides might further allow for selective control of different cell-type invasion. In this study, the invasion of fibroblasts and vascular smooth muscle cells (VSMC) into hydrogels polymerised with either a peptide generally permissive for matrix metalloproteinase (MMP) degradation or peptides preferentially cleaved by MMP-14 or MMP-9 enzymes were compared. The two cell-types invaded the MMP permissive hydrogel equally. However, invasion of VSMC into MMP-14 selective peptide crosslinked hydrogels was diametrically opposite in nature to that of fibroblasts whereby VSMC showed a two-fold increase into these hydrogels relative to that observed in permissive hydrogels whilst fibroblasts had a relative two-fold decrease (p < 0.01). These findings are suggestive that invasion and growth of different cell-types in engineered synthetic extracellular matrix mimics may be controlled selectively by the choice of protease specific peptide crosslinker and this could have general utility in tissue regenerative and engineering approaches. (C) 2013 Elsevier Ltd. All rights reserved.
引用
收藏
页码:6797 / 6803
页数:7
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