Literature DB >> 4057266

Surface ultrastructure of the gill arch of the killifish, Fundulus heteroclitus, from seawater and freshwater, with special reference to the morphology of apical crypts of chloride cells.

F E Hossler, G Musil, K J Karnaky, F H Epstein.   

Abstract

The surface ultrastructure of the gill arches of the killifish, Fundulus heteroclitus, adapted to seawater or freshwater, was found to be similar to that reported for other euryhaline teleosts. Two rows of gill filaments (about 42 filaments per row) extended posterolaterally, and two rows of gill rakers (about 10 rakers per row) extended anteromedially from each arch. Leaf-like respiratory lamellae protruded along both sides of each filament, from its base to its apex. The distributions, sizes, and numbers of various surface cells and structures were also determined. All surfaces were covered by a mosaic of pavement cells, which measured about 7 X 4 microns and exhibited concentrically arranged surface ridges. Taste buds were especially prominent on the rakers and the pharyngeal surfaces of the first and second gill arches, but were often replaced by horny spines on the third and fourth gill arches. Apical crypts of chloride cells occurred mostly on the surfaces of the gill filaments adjacent to the afferent artery of the filament. In seawater adapted killifish, crypts resembled narrow, deep holes along the borders of adjacent pavement cells, had openings of about 2 microns2, and occurred at a frequency of about 1 per 70 microns2 of surface area. In freshwater fish, the crypts usually had larger openings (about 10 microns2), occurred less frequently (1 per 123 microns2), and exhibited many cellular projections in their interiors. Changes in crypt morphology may be related to the ion transport function of chloride cells.

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Year:  1985        PMID: 4057266     DOI: 10.1002/jmor.1051850309

Source DB:  PubMed          Journal:  J Morphol        ISSN: 0022-2887            Impact factor:   1.804


  9 in total

1.  Ontogeny of salinity tolerance and evidence for seawater-entry preparation in juvenile green sturgeon, Acipenser medirostris.

Authors:  Peter J Allen; Maryann McEnroe; Tetyana Forostyan; Stephanie Cole; Mary M Nicholl; Brian Hodge; Joseph J Cech
Journal:  J Comp Physiol B       Date:  2011-06-01       Impact factor: 2.200

2.  Mitochondria-rich cells in the branchial epithelium of the teleost,Oreochromis mossambicus, acclimated to various hypotonic environments.

Authors:  T H Lee; P P Hwang; H C Lin; F L Huang
Journal:  Fish Physiol Biochem       Date:  1996-12       Impact factor: 2.794

3.  Gill morphology in two Mediterranean Sea fishes of similar feeding preferences: sea bream (Sparus aurata L) and sea bass (Dicentrarchus labrax).

Authors:  Mohamed A M Alsafy
Journal:  Vet Res Commun       Date:  2013-03-10       Impact factor: 2.459

4.  Effects of low environmental salinity on the cellular profiles and expression of Na+, K+-ATPase and Na+, K+, 2Cl- cotransporter 1 of branchial mitochondrion-rich cells in the juvenile marine fish Monodactylus argenteus.

Authors:  Chao-Kai Kang; Fu-Chen Liu; Wen-Been Chang; Tsung-Han Lee
Journal:  Fish Physiol Biochem       Date:  2011-08-24       Impact factor: 2.794

5.  Primary culture of gill epithelial cells from the sea bass Dicentrarchus labrax.

Authors:  M Avella; J Berhaut; P Payan
Journal:  In Vitro Cell Dev Biol Anim       Date:  1994-01       Impact factor: 2.416

6.  TEP on the tide in killifish (Fundulus heteroclitus): effects of progressively changing salinity and prior acclimation to intermediate or cycling salinity.

Authors:  Chris M Wood; Martin Grosell
Journal:  J Comp Physiol B       Date:  2008-12-30       Impact factor: 2.200

7.  Structural differentiation of apical openings in active mitochondria-rich cells during early life stages of Nile tilapia (Oreochromis niloticus L.) as a response to osmotic challenge.

Authors:  S Fridman; K J Rana; J E Bron
Journal:  Fish Physiol Biochem       Date:  2013-01-11       Impact factor: 2.794

Review 8.  The fish gill: site of action and model for toxic effects of environmental pollutants.

Authors:  D H Evans
Journal:  Environ Health Perspect       Date:  1987-04       Impact factor: 9.031

9.  Medaka villin 1-like protein (VILL) is associated with the formation of microvilli induced by decreasing salinities in the absorptive ionocytes.

Authors:  Chao-Kai Kang; Tsung-Han Lee
Journal:  Front Zool       Date:  2014-01-13       Impact factor: 3.172

  9 in total

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