2002
DOI: 10.1002/jez.10127
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Na+, Cl, Ca2+ and Zn2+ transport by fish gills: retrospective review and prospective synthesis

Abstract: The secondary active Cl(-) secretion in seawater (SW) teleost fish gills and elasmobranch rectal gland involves basolateral Na(+),K(+)-ATPase and NKCC, apical membrane CFTR anion channels, and a paracellular Na(+)-selective conductance. In freshwater (FW) teleost gill, the mechanism of NaCl uptake is more controversial and involves apical V-type H(+)-ATPase linked to an apical Na(+) channel, apical Cl(-)-HCO-3 exchange and basolateral Na(+),K(+)-ATPase. Ca(2+) uptake (in FW and SW) is via Ca(2+) channels in th… Show more

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Cited by 430 publications
(325 citation statements)
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References 145 publications
(33 reference statements)
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“…Recently, higher protein expression analysed by an anti-rat ClC3 antibody was found in FW pufferfish gills than in SW ones (Tang and Lee, 2007). On the other hand, a cystic fibrosis transmembrane conductance regulator (CFTR) was also proposed to be a candidate for basolateral Cl -exit based on its basolateral localization in pavement and MR cells in killifish operculum (Marshall, 2002). In NCC cells, basolateral NKA may provide the intracellular negative gradient for driving the basolateral Cl -channels to transport Cl -out of NCC cells, as in mammalian DCT cells.…”
Section: Basolateral CL -Transportmentioning
confidence: 99%
“…Recently, higher protein expression analysed by an anti-rat ClC3 antibody was found in FW pufferfish gills than in SW ones (Tang and Lee, 2007). On the other hand, a cystic fibrosis transmembrane conductance regulator (CFTR) was also proposed to be a candidate for basolateral Cl -exit based on its basolateral localization in pavement and MR cells in killifish operculum (Marshall, 2002). In NCC cells, basolateral NKA may provide the intracellular negative gradient for driving the basolateral Cl -channels to transport Cl -out of NCC cells, as in mammalian DCT cells.…”
Section: Basolateral CL -Transportmentioning
confidence: 99%
“…An empty chamber containing the same volume of water but spiked with 22 Na ϩ and/or 36 Cl Ϫ was used as a control. Because rehydration of the gills, a main site of ion regulation in most fish (Perry 1997;Marshall 2002), could also alter ion movements after reimmersion, recovery experiments in water that were similar to those described for 3 H-H 2 O (above) were performed to track ion movements after 4 wk of air exposure. In these experiments, water samples were taken at 0, 2, 4, 8, 12, 16, and 24 h after reimmersion.…”
Section: Experiments 2: Effects Of Air Exposure On 3 H-h 2 O Flux Acromentioning
confidence: 99%
“…Inspection of the electron micrographs and immunohistochemistry of the skin and gills of P. annectens (Sturla et al 2001) suggests the MR cells are fewer in number and size compared to teleosts (Perry 1997;Marshall 2002). These observations, combined with the lungfish's reduced gill (Laurent et al Burggren and Johansen 1986), suggested that P. dolloi would have low basal rates of ion uptake.…”
Section: Ion Uptake Continues In Airmentioning
confidence: 99%
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“…The sodium gradient is then used by a Na + /K + /2Cl -co-transporter (NKCC1) to bring chloride into the cell. Chloride then leaves the cells on a favorable electrochemical gradient through an apical chloride channel, a homolog of the cystic fibrosis transmembrane conductance regulator (CFTR) (Marshall, 2002). In addition to providing the electrochemical gradient for chloride secretion, NKA also pumps sodium into the paracellular space where sodium leaves through leaky tight junctions on a favorable electrochemical gradient.…”
Section: Introductionmentioning
confidence: 99%