Literature DB >> 12242705

The physiology of flatfish chromatophores.

Derek Burton1.   

Abstract

Most flatfish, of the order Pleuronectiformes, possess a white lower side, and a brown or grey upper side. This upper side can display integumentary patterning with dark areas and colored or white spots. Chromatophores in flatfish are dermal and epidermal melanophores, as well as dermal xanthophores, erythrophores, iridophores, and leucophores, combinations of which contribute to the color and patterning. Cellular studies demonstrate pattern-related differences in numerical distribution between the types of chromatophores, and in their size, both of which will enhance contrast between areas of the pattern. As well as these morphological characteristics, there are also clear physiological differences, with melanophores from various areas of the patterns demonstrating differential responsiveness to background and to stress/excitement stimuli. Regulation of flatfish melanophore responses is predominantly neural, through the sympathetic nervous system; the pituitary hormones in these fish function in maintaining final equilibria in physiological adaptations to backgrounds. Melanophores from main components of patterns also respond differently in vitro to electrical stimulation, to pituitary hormones, and to sympathomimetic drugs and their antagonists. Sensitivity characteristics with alpha- and beta-adrenergic pharmacological reagents in vitro indicate the existence of a pattern-related balance in alpha- and beta-adrenoceptor mediation in melanophore regulation. The patterning mechanism is complex, with both morphological and physiological differences at the chromatophore level, as well as involvement of central processing and control, which remains to be analysed. Copyright 2002 Wiley-Liss, Inc.

Mesh:

Year:  2002        PMID: 12242705     DOI: 10.1002/jemt.10166

Source DB:  PubMed          Journal:  Microsc Res Tech        ISSN: 1059-910X            Impact factor:   2.769


  4 in total

1.  Comparison of pigment cell ultrastructure and organisation in the dermis of marble trout and brown trout, and first description of erythrophore ultrastructure in salmonids.

Authors:  Ida Djurdjevič; Mateja Erdani Kreft; Simona Sušnik Bajec
Journal:  J Anat       Date:  2015-09-11       Impact factor: 2.610

2.  Changeable camouflage: how well can flounder resemble the colour and spatial scale of substrates in their natural habitats?

Authors:  Derya Akkaynak; Liese A Siemann; Alexandra Barbosa; Lydia M Mäthger
Journal:  R Soc Open Sci       Date:  2017-03-08       Impact factor: 2.963

3.  Comparative transcriptome analysis of trout skin pigment cells.

Authors:  Ida Djurdjevič; Tomasz Furmanek; Seita Miyazawa; Simona Sušnik Bajec
Journal:  BMC Genomics       Date:  2019-05-09       Impact factor: 3.969

4.  Coordinated regulation of chromatophore differentiation and melanogenesis during the ontogeny of skin pigmentation of Solea senegalensis (Kaup, 1858).

Authors:  Maria J Darias; Karl B Andree; Anaïs Boglino; Ignacio Fernández; Alicia Estévez; Enric Gisbert
Journal:  PLoS One       Date:  2013-05-09       Impact factor: 3.240

  4 in total

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