Fibronectin peptides mediate HMEC adhesion to porcine-derived extracellular matrix

被引:78
作者
Hodde, J
Record, R
Tullius, R
Badylak, S
机构
[1] Cook Biotech Inc, W Lafayette, IN 47906 USA
[2] Purdue Univ, Dept Biomed Engn, W Lafayette, IN 47907 USA
关键词
small intestinal submucosa; endothelial cell; adhesion; fibronectin; integrins; extracellular matrix;
D O I
10.1016/S0142-9612(01)00310-6
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Extracellular matrices (ECM) derived from porcine tissues have been shown to support the successful repair and remodeling of injured tissues when evaluated in animal models. Cell-matrix interactions, including ligand-integrin associations that facilitate endothelial cell adhesion, are clearly important in the tissue remodeling process. The goal of the present study was to identify the peptide sequences within the ubiquitous protein fibronectin (FN) that may be important in the initial interactions between the host endothelial cells and the ECM scaffold. Human microvascular endothelial cells (HMEC) were seeded upon porcine ECM after having been subjected to pretreatment with peptide ligands derived from tissue FN and were allowed to attach for 20 min. Non-adherent cells were removed and the remaining, tritium-labeled cells attached to the ECM were counted. Results showed that cyclo-RGD and REDV, but not LDV or PHSRN, play a role in mediating the attachment of HMEC to porcine ECM. (C) 2002 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:1841 / 1848
页数:8
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