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The potential applications of fibrin-coated electrospun polylactide nanofibers in skin tissue engineering
M. Bacakova, J. Musilkova, T. Riedel, D. Stranska, E. Brynda, M. Zaloudkova, L. Bacakova,
Language English Country New Zealand
Document type Journal Article, Research Support, Non-U.S. Gov't
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PubMed
26955273
DOI
10.2147/ijn.s99317
Knihovny.cz E-resources
- MeSH
- Cell Differentiation MeSH
- Electrochemistry methods MeSH
- Extracellular Matrix metabolism MeSH
- Fibrin chemistry metabolism MeSH
- Fibroblasts cytology metabolism MeSH
- Fluorescent Antibody Technique MeSH
- Immunoenzyme Techniques MeSH
- Collagen genetics metabolism MeSH
- Cells, Cultured MeSH
- Skin cytology metabolism MeSH
- Real-Time Polymerase Chain Reaction MeSH
- Humans MeSH
- RNA, Messenger genetics MeSH
- Nanofibers chemistry MeSH
- Polyesters chemistry MeSH
- Reverse Transcriptase Polymerase Chain Reaction MeSH
- Cell Proliferation MeSH
- Regeneration physiology MeSH
- Tissue Engineering methods MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
Fibrin plays an important role during wound healing and skin regeneration. It is often applied in clinical practice for treatment of skin injuries or as a component of skin substitutes. We prepared electrospun nanofibrous membranes made from poly(l-lactide) modified with a thin fibrin nanocoating. Fibrin surrounded the individual fibers in the membrane and also formed a thin fibrous mesh on several places on the membrane surface. The cell-free fibrin nanocoating remained stable in the cell culture medium for 14 days and did not change its morphology. On membranes populated with human dermal fibroblasts, the rate of fibrin degradation correlated with the degree of cell proliferation. The cell spreading, mitochondrial activity, and cell population density were significantly higher on membranes coated with fibrin than on nonmodified membranes, and this cell performance was further improved by the addition of ascorbic acid in the cell culture medium. Similarly, fibrin stimulated the expression and synthesis of collagen I in human dermal fibroblasts, and this effect was further enhanced by ascorbic acid. The expression of beta1-integrins was also improved by fibrin, and on pure polylactide membranes, it was slightly enhanced by ascorbic acid. In addition, ascorbic acid promoted deposition of collagen I in the form of a fibrous extracellular matrix. Thus, the combination of nanofibrous membranes with a fibrin nanocoating and ascorbic acid seems to be particularly advantageous for skin tissue engineering.
2nd Faculty of Medicine Charles University Prague Prague Czech Republic
InStar Technologies Liberec Czech Republic
Institute of Macromolecular Chemistry Czech Academy of Sciences Prague Czech Republic
Institute of Rock Structure and Mechanics Czech Academy of Sciences Prague Czech Republic
References provided by Crossref.org
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