Relationships among cell attachment, spreading, cytoskeletal organization,and migration rate for anchorage-dependent cells on model surfaces

Citation
K. Webb et al., Relationships among cell attachment, spreading, cytoskeletal organization,and migration rate for anchorage-dependent cells on model surfaces, J BIOMED MR, 49(3), 2000, pp. 362-368
Citations number
34
Categorie Soggetti
Multidisciplinary
Journal title
JOURNAL OF BIOMEDICAL MATERIALS RESEARCH
ISSN journal
00219304 → ACNP
Volume
49
Issue
3
Year of publication
2000
Pages
362 - 368
Database
ISI
SICI code
0021-9304(20000305)49:3<362:RACASC>2.0.ZU;2-C
Abstract
Many research and commercial applications use a synthetic substrate which i s seeded with cells in a serum-containing medium. The surface properties of the material influence the composition of the adsorbed protein layer, whic h subsequently regulates a variety of cell behaviors such as attachment, sp reading, proliferation, migration, and differentiation. In this study, we e xamined the relationships among cell attachment, spreading, cytoskeletal or ganization, and migration rate for MC3T3-E1. osteoblasts on glass surfaces modified with SOx, -NH2, -N+(CH3)(3), -SH, and -CH3 terminal silanes, We al so studied the relationship between cell spread area and migration rate for a variety of anchorage-dependent cell types on a model polymeric biomateri al, poly(acrylonitrile-vinylchloride). Our results indicated that MC3T3-E1 osteoblast behavior was surface chemistry dependent, and varied with indivi dual functional groups rather than general surface properties such as wetta bility. In addition, cell migration rate was inversely related to cell spre ad area for MC3T3-E1 osteoblasts on a variety of silane-modified surfaces a s well as for different anchorage-dependent cell types on a model polymeric biomaterial. Furthermore, the data revealed significant differences in mig ration rate among different cell types on a common polymeric substrate, sug gesting that cell type-specific differences must be considered when using, selecting, or designing a substrate for research and therapeutic applicatio ns. (C) 2000 John Wiley & Sons, Inc.