A NOVEL ARTIFICIAL SUBSTRATE FOR CELL-CULTURE - EFFECTS OF SUBSTRATE FLEXIBILITY MALLEABILITY ON CELL-GROWTH AND MORPHOLOGY/

Citation
Hp. Hohn et al., A NOVEL ARTIFICIAL SUBSTRATE FOR CELL-CULTURE - EFFECTS OF SUBSTRATE FLEXIBILITY MALLEABILITY ON CELL-GROWTH AND MORPHOLOGY/, In vitro cellular & developmental biology. Animal, 31(1), 1995, pp. 37-44
Citations number
44
Categorie Soggetti
Developmental Biology","Cell Biology
ISSN journal
10712690
Volume
31
Issue
1
Year of publication
1995
Pages
37 - 44
Database
ISI
SICI code
1071-2690(1995)31:1<37:ANASFC>2.0.ZU;2-C
Abstract
Gels of glyoxyl agarose (GA) are evaluated as a novel flexible substra te for cell culture with physical properties comparable to extracellul ar matrix (ECM) gels. We show here that cells adhere well to pure GA g els; in addition, specific interactions involving matrix receptors can be studied when individual matrix molecules are bound to the gel cova lently. When cells are grown on such substrates, morphology is compara ble to that observed on ''natural'' matrix gels (reconstituted gels of collagen type I or of Matrigel): rather than being flattened as in mo nolayer cultures on tissue culture plastic the cells assume a rounded morphology and tend to form tissue-like aggregates. The effects of the artificial matrix gels are discussed in the context of previous publi cations on cell interactions with the extracellular matrix, suggesting that in addition to specific recognition of matrix molecules the phys ical properties of ECM by themselves can be decisive for cell differen tiation. We conclude that gels of glyoxyl agarose a) provide a useful model to mimic the physical properties of matrix gels without the pres ence of specific adhesion factors; b) may be useful as a general, non- specific ECM allowing cells to be cultured in vitro under conditions f avorable for differentiation; and cf allow to design a variety of ''sy nthetic'' ECM models composed of a chemically defined gel matrix, whic h can be supplemented with covalently bound molecules to be recognized by cell surface receptors.