KINETICS OF BONE CELL ORGANIZATION AND MINERALIZATION ON MATERIALS WITH PATTERNED SURFACE-CHEMISTRY

Citation
Ke. Healy et al., KINETICS OF BONE CELL ORGANIZATION AND MINERALIZATION ON MATERIALS WITH PATTERNED SURFACE-CHEMISTRY, Biomaterials, 17(2), 1996, pp. 195-208
Citations number
61
Categorie Soggetti
Engineering, Biomedical","Materials Science, Biomaterials
Journal title
ISSN journal
01429612
Volume
17
Issue
2
Year of publication
1996
Pages
195 - 208
Database
ISI
SICI code
0142-9612(1996)17:2<195:KOBCOA>2.0.ZU;2-H
Abstract
Materials with spatially resolved chemistries (i.e. patterned surfaces ) have been used to guide and organize the position of mammalian cells in vitro. A common theme in guiding the spatial distribution of cells has been the use of patterned alkylsiloxanes, where one region contai ns an aminosilane and the other an alkylsilane. The regions of the ami nosilane served as preferential sites for cell attachment and spreadin g, presumably dependent on the association between cell surface proteo glycans the positively charged amine. In this study, experiments were conducted with patterns of N-(2-aminoethyl)-3-aminopropyl-trimethoxysi lane (EDS) and dimethyldichlorosilane (DMS) to determine the kinetics of spatial organization of bone-derived cells, and whether initial att achment and spreading affected the rate of matrix mineralization (i.e. bone formation) in extended cultures. The bone cells required the pre sence of serum or preadsorption of serum proteins to the patterned EDS /DMS surface to organize according to the lithographically defined sur face chemistry. Time-lapse video microscopy indicated that cells were randomly distributed over the EDS/DMS surface at the time of plating, but organized on the EDS regions within 30 min. When cultures were ext ended for 15 and 25 days, the matrix synthesized by the cells was pref erentially mineralized on the EDS chemistry. These results demonstrate the ability of surface chemistry modifications to organize cells and form mineralized tissue in vitro. The methods employed should have gen eral value to the engineering of tissues in vitro.