Characterization of Melanophore Morphology by Fractal Dimension Analysis

• Published in: Pigment cell research Vol. 17; no. 2; pp. 165 - 172
• Main Authors: Kimler, Victoria A., Tracy-Bee, Mary, Ollie, Candace D., Langer, Renee M., Montante, James M., Marks, Charles R. C., Carl Freeman, D., Anton Hough, R., Taylor, John D.
• Format: Journal Article
• Language: English
• Published: Oxford, UK Munksgaard International Publishers 01.04.2004
• Subjects: Animals; Caffeine - pharmacology; Cell Membrane - metabolism; Cell perimeter; Chromatophores; Cortical actin; Cytoskeleton - metabolism; Epinephrine - pharmacology; Focal dimension analysis; Fractal dimension analysis; Fractals; Fundulidae; Melanocytes - metabolism; Melanophores; Melanophores - cytology; Melanosomes - metabolism; Microscopy, Fluorescence - methods; Morphometrics; Neurons - pathology; Phosphodiesterase Inhibitors - pharmacology; Protein Transport; Time Factors
• ISSN: 0893-5785; 1600-0749
• DOI: 10.1046/j.1600-0749.2003.00125.x

Fractal or focal dimension (FD) analysis is a valuable tool to identify physiologic stimuli at the cellular and tissue levels that allows for quantification of cell perimeter complexity. The FD analysis was determined on fluorescence images of caffeine‐ or epinephrine‐treated (or untreated control) killifish Fundulus heteroclitus (Linneaus) melanophores in culture. Cell perimeters were indicated by rhodamine‐phalloidin labeling of cortical microfilaments using box‐counting FD analysis. Caffeine‐treated melanophores displayed dispersed melanosomes in cells with less serrated edges and reduced FD and complexity. Complexity in epinephrine‐treated cells was significantly higher than the caffeine‐treated cells or in the control. Cytoarchitectural variability of the cell perimeter is expected because cells change shape when cued with agents. Epinephrine‐treated melanophores demonstrated aggregated melanosomes in cells with more serrated edges, significantly higher FD and thus complexity. Melanophores not treated with caffeine or epinephrine produced variable distributions of melanosomes and resulted in cells with variably serrated edges and intermediate FD with a larger SE of the regression and greater range of complexity. Dispersion of melanosomes occurs with rearrangements of the cytoskeleton to accommodate centrifugal distribution of melanosomes throughout the cell and to the periphery. The loading of melanosomes onto cortical microfilaments may provide a less complex cell contour, with the even distribution of the cytoskeleton and melanosomes. Aggregation of melanosomes occurs with rearrangements of the cytoskeleton to accommodate centripetal distribution of melanosomes. The aggregation of melanosomes may contribute to centripetal retraction of the cytoskeleton and plasma membrane. The FD analysis is, therefore, a convenient method to measure contrasting morphologic changes within stimulated cells.