Under serum-free conditions, rat skin fibroblasts, but not cortical astrocy
tes, selectively adhered to glass surfaces modified with the integrin-ligan
d peptide RGDS. In contrast, astrocytes, but not fibroblasts, exhibited enh
anced adhesion onto substrates modified with KHIFSDDSSE, a peptide that mim
ics a homophilic binding domain of neural cell adhesion molecule (NCAM). As
trocyte and fibroblast adhesion onto substrates modified with the integrin
ligands IKVAV and YIGSR as well as the control peptides RDGS and SEDSDKFISH
were similar to that observed on aminophase glass (reference substrate). T
his study is the first to demonstrate the use of immobilized KHIFSDDSSE in
selectively modulating astrocyte and fibroblast adhesion on material surfac
es, potentially leading to materials that promote specific functions of cel
ls involved in the response(s) of central nervous system tissues to injury.
This information could be incorporated into novel biomaterials designed to
improve the long-term performance of the next generation of neural prosthe
ses. (C) 2001 Elsevier Science Ltd. All rights reserved.