Osteoblast population migration characteristics on substrates modified with immobilized adhesive peptides

Citation
Kc. Dee et al., Osteoblast population migration characteristics on substrates modified with immobilized adhesive peptides, BIOMATERIAL, 20(3), 1999, pp. 221-227
Citations number
35
Categorie Soggetti
Multidisciplinary
Journal title
BIOMATERIALS
ISSN journal
01429612 → ACNP
Volume
20
Issue
3
Year of publication
1999
Pages
221 - 227
Database
ISI
SICI code
0142-9612(199902)20:3<221:OPMCOS>2.0.ZU;2-V
Abstract
The process of cell migration is inextricably linked with the process of ce ll adhesion and, therefore, with cell/substrate adhesiveness. The present s tudy adapted an under-agarose cell migration assay to quantitatively examin e population migration characteristics of osteoblasts, on substrates modifi ed with adhesive peptides, in the absence and presence of growth factors. S hort-term, that is, 48 h osteoblast migration distances on substrates modif ied with adhesive Arg-Gly-Asp-Ser peptides were significantly(P < 0.05) les s than migration distances on substrates modified with non-adhesive Arg-Asp -Cly-Ser peptides, demonstrating that osteoblast population haptokinesis wa s significantly decreased on substrates modified with adhesive peptides. Ra ndom motility coefficients calculated in the present study for osteoblast p opulations were an order of magnitude lower than a published random motilit y coefficient for leukocytes, proving quantitatively that, compared to leuk ocytes, osteoblasts migrate via haptokinesis more slowly. The 48 and 72 h o steoblast population migration differentials in the presence of an initial mass of 60 ng of basic Fibroblast Growth Factor, on substrates modified wit h Arg-Gly-Asp-Ser or with Arg-Asp-Gly-Ser, were larger than all other chemo tactic differentials on these substrates. Quantitative investigations (such as the present study) of cell population migration characteristics on mode l biomaterial surfaces will become increasingly necessary as the discipline of cell/tissue engineering matures. (C) 1999 Elsevier Science Ltd. All rig hts reserved.