Fibroblasts retain their tissue phenotype when grown in three-dimensional collagen gels

• Published in: Experimental cell research Vol. 195; no. 2; pp. 432 - 442
• Main Authors: Doane, Kathleen J., Birk, David E.
• Format: Journal Article
• Language: English
• Published: Orlando, FL Elsevier Inc 1991; Elsevier
• Subjects: Animal cells; Animals; Biological and medical sciences; Cell cultures. Hybridization. Fusion; Cell Division; Cells, Cultured; Chick Embryo; Collagen; Cornea - cytology; Culture Media; Fibroblasts - cytology; Fundamental and applied biological sciences. Psychology; Gels; Microscopy, Fluorescence; Molecular and cellular biology; Phenotype; Skin - cytology; Tendons - cytology; Culture medium; Confocal system; Tissue specificity; Orientation; Vertebrata; Phenotype; Fluorescent labelling; Collagen; Morphology; Isolation; Extracellular matrix; Chicken; Aves; Fibroblast
• ISSN: 0014-4827; 1090-2422
• DOI: 10.1016/0014-4827(91)90394-A

Fibroblasts are responsible for the synthesis, assembly, deposition, and organization of extracellular matrix molecules, and thus determine the morphology of connective tissues. Deposition of matrix molecules occurs in extracellular compartments, where the sequential stages are under cellular control. Cell orientation/ polarity is important in determining how the cell orients these extracytoplasmic compartments and therefore how the matrix is assembled and oriented. However, the control of cell orientation is not understood. Fibroblasts from three tissues with different morphologies were studied to determine whether cells maintained their characteristic phenotype. Fibroblasts from cornea, which in vivo are oriented in orthogonal layers along with their matrix; from tendon, a uniaxial connective tissue, where cells orient parallel to each other; and from dermis, a connective tissue with no apparent cellular orientation, were used to study cell morphology and orientation in three-dimensional collagen gels. The different cells were grown for 3 and 7 days in identical three-dimensional collagen gels with a nonoriented matrix. Confocal fluorescence microscopy demonstrated that corneal fibroblasts oriented perpendicular to one another at 3 days, and after 7 days in hydrated gels these cells formed orthogonal sheets. Tendon fibroblasts were shown by the same methods to orient parallel to one another in bundles at both 3 and 7 days, throughout the depth of the gel. Dermal fibroblasts showed no apparent orientation throughout the hydrated gels at either time point examined. The organization of these different cell types was consistent with their tissue of origin as was the cell structure and polarity. These studies imply that cellular and tissue phenotype is innate to differentiated fibroblasts and that these cells will orient in a tissue-specific manner regardless of the extracellular matrix present.