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Morphology of a fibrin nanocoating influences dermal fibroblast behavior
J. Pajorova, M. Bacakova, J. Musilkova, A. Broz, D. Hadraba, F. Lopot, L. Bacakova,
Language English Country New Zealand
Document type Journal Article
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PubMed
29922057
DOI
10.2147/ijn.s162644
Knihovny.cz E-resources
- MeSH
- Cell Adhesion physiology MeSH
- Cell Culture Techniques instrumentation methods MeSH
- Extracellular Matrix metabolism MeSH
- Fibrin chemistry pharmacology MeSH
- Fibroblasts cytology drug effects MeSH
- Fibronectins metabolism MeSH
- Collagen Type I metabolism MeSH
- Cells, Cultured MeSH
- Skin cytology MeSH
- Humans MeSH
- Membranes, Artificial MeSH
- Nanostructures chemistry MeSH
- Nanotechnology methods MeSH
- Polyesters chemistry MeSH
- Cell Proliferation physiology MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
Background: Our study focuses on the fabrication of appropriate scaffolds for skin wound healing. This research brings valuable insights into the molecular mechanisms of adhesion, proliferation, and control of cell behavior through the extracellular matrix represented by synthetic biodegradable nanofibrous membranes coated by biomolecules. Methods: Nanofibrous polylactic acid (PLA) membranes were prepared by a needle-less electrospinning technology. These membranes were coated with fibrin according to two preparation protocols, and additionally they were coated with fibronectin in order to increase the cell affinity for colonizing the PLA membranes. The adhesion, growth, and extracellular matrix protein production of neonatal human dermal fibroblasts were evaluated on the nanofibrous membranes. Results: Our results showed that fibrin-coated membranes improved the adhesion and proliferation of human dermal fibroblasts. The morphology of the fibrin nanocoating seems to be crucial for the adhesion of fibroblasts, and consequently for their phenotypic maturation. Fibrin either covered the individual fibers in the membrane (F1 nanocoating), or covered the individual fibers and also formed a fine homogeneous nanofibrous mesh on the surface of the membrane (F2 nanocoating), depending on the mode of fibrin preparation. The fibroblasts on the membranes with the F1 nanocoating remained in their typical spindle-like shape. However, the cells on the F2 nanocoating were spread mostly in a polygon-like shape, and their proliferation was significantly higher. Fibronectin formed an additional mesh attached to the surface of the fibrin mesh, and further enhanced the cell adhesion and growth. The relative gene expression and protein production of collagen I and fibronectin were higher on the F2 nanocoating than on the F1 nanocoating. Conclusion: A PLA membrane coated with a homogeneous fibrin mesh seems to be promising for the construction of temporary full-thickness skin tissue substitutes.
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