Abstract
Cell adhesion to adsorbed proteins and adhesive sequences engineered on surfaces is crucial to cellular and host responses to implanted devices, biological integration of biomaterials and tissue-engineered constructs, and the performance of biosensors, cell-based arrays, and biotechnological cell-culture supports. This review focuses on interfaces controlling cell-adhesive interactions, with particular emphasis on surfaces controlling protein adsorption, biomimetic substrates presenting bioadhesive motifs, and micropatterned surfaces to engineer adhesive areas. These approaches represent promising strategies to engineer cell-material biomolecular interactions in order to elicit specific cellular responses and enhance the biological performance of materials in biomedical and biotechnological applications.
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Abbreviations
- COL-I:
-
Type I collagen
- ECM:
-
Extracellular matrix
- ELISA:
-
Enzyme-linked immunosorbent assay
- FN:
-
Fibronectin
- GFOGER:
-
Glycine-phenylalanine-hydroxyproline-glycine-glutamate-arginine
- LN:
-
Laminin
- PEG:
-
Poly(ethelyne glycol)
- RGD:
-
Arginine-glycine-aspartic acid
- SAM:
-
Self-assembled monolayers
- YIGSR:
-
Tyrosine-isoleucine-glycine-serine-arginine
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Acknowledgments
AJG gratefully acknowledges support from the National Science Foundation, National Institutes of Health, Arthritis Foundation, Whitaker Foundation, and the Georgia Tech/Emory NSF ERC on Engineering Living Tissues.
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García, A.J. Interfaces to Control Cell-Biomaterial Adhesive Interactions. In: Werner, C. (eds) Polymers for Regenerative Medicine. Advances in Polymer Science, vol 203. Springer, Berlin, Heidelberg. https://doi.org/10.1007/12_071
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DOI: https://doi.org/10.1007/12_071
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