Cell-matrix and cell-cell interactions of human gingival fibroblasts on three-dimensional nanofibrous gelatin scaffolds

被引:20
|
作者
Sachar, Ashneet [1 ]
Strom, T. Amanda [1 ]
San Miguel, Symone [1 ]
Serrano, Maria J. [1 ]
Svoboda, Kathy K. H. [1 ]
Liu, Xiaohua [1 ]
机构
[1] Texas A&M Univ, Hlth Sci Ctr, Baylor Coll Dent, Dept Biomed Sci, Dallas, TX 75246 USA
基金
美国国家卫生研究院;
关键词
confocal microscopy; gelatin scaffold; human gingival fibroblast; cell-material interaction; three-dimensional; biomimetic; FOCAL ADHESION DYNAMICS; EXTRACELLULAR-MATRIX; COLLAGEN LATTICES; ACTIN CYTOSKELETON; INTERFERENCE REFLECTION; CONTACT INHIBITION; JUNCTION FORMATION; MELANOMA-CELLS; MIGRATION; BEHAVIOR;
D O I
10.1002/term.1588
中图分类号
Q813 [细胞工程];
学科分类号
摘要
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.
引用
收藏
页码:862 / 873
页数:12
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