An in-depth understanding of the interactions between cells and three-dimensional (3D) matrices (scaffolds) is pivotal to the development of novel biomaterials for tissue regeneration. However, it remains a challenge to find suitable biomimetic substrates and tools to observe cell-material and cell-cell interactions on 3D matrices. In the present study, we developed biomimetic nanofibrous 3D gelatin scaffolds (3D-NF-GS) and utilized confocal microscopy combined with a quantitative analysis approach to explore cell-matrix and cell-cell interactions on the 3D-NF-GS. Human gingival fibroblasts (HGFs) migrated throughout the 3D-NF-GS by 5 days and formed stable focal adhesions by 14 days. The focal adhesions were detected using integrin-1, phospho-paxillin and vinculin expression, which were quantified from specific wavelength photon data generated using a spectral separation confocal microscope. As the cells became more confluent after 14 days of culture, cell-cell communication via gap junctions increased significantly. Collagen I matrix production by HGFs on 3D-NF-GS was visualized and quantified using a novel approach incorporating TRITC label in the scaffolds. Based on confocal microscopy, this study has developed qualitative and quantitative methods to study cell-matrix and cell-cell interactions on biomimetic 3D matrices, which provides valuable insights for the development of appropriate scaffolds for tissue regeneration. Copyright (c) 2012 John Wiley & Sons, Ltd.
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Univ Manchester, Fac Biol Med & Hlth, Off Business Relat, Manchester, Lancs, EnglandUniv Nottingham, Sch Med, Div Canc & Stem Cells, Stem Cell Glycobiol Grp, Nottingham, England
Meade, K. A.
Thompson, A.
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Univ Nottingham, Sch Med, Div Canc & Stem Cells, Nottingham, EnglandUniv Nottingham, Sch Med, Div Canc & Stem Cells, Stem Cell Glycobiol Grp, Nottingham, England
Thompson, A.
Arkill, K. P.
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Univ Nottingham, Sch Med, Div Canc & Stem Cells, Nottingham, EnglandUniv Nottingham, Sch Med, Div Canc & Stem Cells, Stem Cell Glycobiol Grp, Nottingham, England
Arkill, K. P.
Tassieri, M.
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Univ Glasgow, Sch Engn, Div Biomed Engn, Glasgow, Lanark, ScotlandUniv Nottingham, Sch Med, Div Canc & Stem Cells, Stem Cell Glycobiol Grp, Nottingham, England
Tassieri, M.
Wright, A. J.
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Univ Nottingham, Fac Engn, Opt & Photon Res Grp, Nottingham, EnglandUniv Nottingham, Sch Med, Div Canc & Stem Cells, Stem Cell Glycobiol Grp, Nottingham, England
Wright, A. J.
Farnie, G.
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Univ Manchester, Manchester Canc Res Ctr, Div Mol & Clin Canc Sci, Manchester, Lancs, England
Univ Oxford, Botnar Res Ctr, SGC, NDORMS, Oxford, EnglandUniv Nottingham, Sch Med, Div Canc & Stem Cells, Stem Cell Glycobiol Grp, Nottingham, England
Farnie, G.
Merry, C. L. R.
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Univ Nottingham, Sch Med, Div Canc & Stem Cells, Stem Cell Glycobiol Grp, Nottingham, EnglandUniv Nottingham, Sch Med, Div Canc & Stem Cells, Stem Cell Glycobiol Grp, Nottingham, England
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Yale Univ, Dept Pathol, Sch Med, New Haven, CT 06510 USA
Natl Canc Ctr, Res Inst, Div Canc Biol, Chuo Ku, Tokyo 104, JapanYale Univ, Dept Pathol, Sch Med, New Haven, CT 06510 USA
Tsuneki, Masayuki
Madri, Joseph A.
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Yale Univ, Dept Pathol, Sch Med, New Haven, CT 06510 USAYale Univ, Dept Pathol, Sch Med, New Haven, CT 06510 USA
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INSERM, Lab Osteoblast Biol & Pathol, U606, F-75475 Paris 10, France
Univ Paris 07, Hop Lariboisiere, F-75475 Paris 10, FranceINSERM, Lab Osteoblast Biol & Pathol, U606, F-75475 Paris 10, France