Tissue spreading on implantable substrates is a competitive outcome of cell–cell vs. cell–substratum adhesivity
Open Access
- 27 March 2001
- journal article
- research article
- Published by Proceedings of the National Academy of Sciences in Proceedings of the National Academy of Sciences
- Vol. 98 (8) , 4323-4327
- https://doi.org/10.1073/pnas.071615398
Abstract
While the interactions of cells with polymeric substrata are widely studied, the influence of cell–cell cohesivity on tissue spreading has not been rigorously investigated. Here we demonstrate that the rate of tissue spreading over a two-dimensional substratum reflects a competition or “tug-of-war” between cell–cell and cell–substratum adhesions. We have generated both a “library” of structurally related copolymeric substrata varying in their adhesivity to cells and a library of genetically engineered cell populations varying only in cohesivity. Cell–substratum adhesivity was varied through the poly(ethylene glycol) content of a series of copolymeric substrata, whereas cell–cell cohesivity was varied through the expression of the homophilic cohesion molecules N- and R-cadherin by otherwise noncohesive L929 cells. In the key experiment, multicellular aggregates containing about 600 cells were allowed to spread onto copolymeric surfaces. We compared the spreading behavior of aggregates having different levels of cell–cell cohesivity on a series of copolymeric substrata having different levels of cell–substratum adhesivity. In these experiments, cell–cell cohesivity was measured by tissue surface tensiometry, and cell–substratum adhesivity was assessed by a distractive method. Tissue spreading was assayed by confocal microscopy as the rate of cell emigration from similar-sized, fluorescence-labeled, multicellular aggregates deposited on each of the substrata. We demonstrate that either decreasing substratum adhesivity or increasing cell–cell cohesivity dramatically slowed the spreading rate of cell aggregates.Keywords
This publication has 38 references indexed in Scilit:
- Tyrosine–PEG-derived poly(ether carbonate)s as new biomaterialsBiomaterials, 1999
- Integrin-ligand binding properties govern cell migration speed through cell-substratum adhesivenessNature, 1997
- Mechanism for transition from initial to stable cell-cell adhesion: kinetic analysis of E-cadherin-mediated adhesion using a quantitative adhesion assay.The Journal of cell biology, 1996
- Laminin-binding integrins in tumor progression and metastasisSeminars in Cancer Biology, 1996
- Cell Migration: A Physically Integrated Molecular ProcessPublished by Elsevier ,1996
- The cadherin-binding specificities of B-cadherin and LCAM.The Journal of cell biology, 1995
- Tyrosine‐derived polycarbonates: Backbone‐modified “pseudo”‐poly(amino acids) designed for biomedical applicationsBiopolymers, 1992
- Motility of fibronectin receptor-deficient cells on fibronectin and vitronectin: collaborative interactions among integrins [published erratum appears in J Cell Biol 1992 Jul;118(1):217]The Journal of cell biology, 1992
- Expressed recombinant cadherins mediate cell sorting in model systemsCell, 1988
- Studies on intercellular adhesive selectivityDevelopmental Biology, 1968