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  • 1
    Online Resource
    Online Resource
    American Physiological Society ; 2008
    In:  American Journal of Physiology-Cell Physiology Vol. 294, No. 5 ( 2008-05), p. C1250-C1260
    In: American Journal of Physiology-Cell Physiology, American Physiological Society, Vol. 294, No. 5 ( 2008-05), p. C1250-C1260
    Abstract: H + -ATPase-rich (HR) cells in zebrafish gills/skin were found to carry out Na + uptake and acid-base regulation through a mechanism similar to that which occurs in mammalian proximal tubular cells. However, the roles of carbonic anhydrases (CAs) in this mechanism in zebrafish HR cells are still unclear. The present study used a functional genomic approach to identify 20 CA isoforms in zebrafish. By screening with whole mount in situ hybridization, only zca2-like a and zca15a were found to be expressed in specific groups of cells in zebrafish gills/skin, and further analyses by triple in situ hybridization and immunocytochemistry demonstrated specific colocalizations of the two zca isoforms in HR cells. Knockdown of zca2-like a caused no change in and knockdown of zca15a caused an increase in H + activity at the apical surface of HR cells at 24 h postfertilization (hpf). Later, at 96 hpf, both the zca2-like a and zca15a morphants showed decreased H + activity and increased Na + uptake, with concomitant upregulation of znhe3b and downregulation of zatp6v1a (H + -ATPase A-subunit) expressions. Acclimation to both acidic and low-Na + fresh water caused upregulation of zca15a expression but did not change the zca2-like a mRNA level in zebrafish gills. These results provide molecular physiological evidence to support the roles of these two zCA isoforms in Na + uptake and acid-base regulation mechanisms in zebrafish HR cells.
    Type of Medium: Online Resource
    ISSN: 0363-6143 , 1522-1563
    Language: English
    Publisher: American Physiological Society
    Publication Date: 2008
    detail.hit.zdb_id: 1477334-X
    SSG: 12
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  • 2
    Online Resource
    Online Resource
    American Physiological Society ; 2011
    In:  American Journal of Physiology-Cell Physiology Vol. 300, No. 2 ( 2011-02), p. C295-C307
    In: American Journal of Physiology-Cell Physiology, American Physiological Society, Vol. 300, No. 2 ( 2011-02), p. C295-C307
    Abstract: Similar to mammalian proximal tubular cells, H + -ATPase rich (HR) cells in zebrafish skin and gills are also responsible for Na + uptake and acid secretion functions. However, the basolateral transport pathways in HR cells are still unclear. In the present study, we tested the hypothesis if there are specific slc4 members involved in basolateral ion transport pathways in HR cells. Fourteen isoforms were identified in the zebrafish(z) slc4 family, and the full-length cDNAs of two novel isoforms, z slc4a1b (anion exchanger, zAE1b) and z slc4a4b (Na + /HCO 3 − cotransporter, zNBCe1b), were sequenced. mRNA signals of z slc4a1b and z slc4a4b were mainly detected in certain groups of ionocytes in zebrafish skin/gills. Further double immunocytochemistry or in situ hybridization demonstrated that zAE1b, but not zNBCe1b, was localized to basolateral membranes of HR cells. Acclimation to low-Na + or acidic environments stimulated the mRNA expression of z slc4a1b in zebrafish gills, and loss-of-function of zslc4a1b with specific morpholinos caused significant decreases in both the whole body Na + content and the skin H + activity in the morphants. On the basis of these results, it was concluded that zAE1b, but not zNBCe1b, is involved in the basolateral transport pathways in Na + uptake/acid secretion mechanisms in zebrafish HR cells.
    Type of Medium: Online Resource
    ISSN: 0363-6143 , 1522-1563
    Language: English
    Publisher: American Physiological Society
    Publication Date: 2011
    detail.hit.zdb_id: 1477334-X
    SSG: 12
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  • 3
    Online Resource
    Online Resource
    American Physiological Society ; 2009
    In:  American Journal of Physiology-Regulatory, Integrative and Comparative Physiology Vol. 296, No. 4 ( 2009-04), p. R1192-R1201
    In: American Journal of Physiology-Regulatory, Integrative and Comparative Physiology, American Physiological Society, Vol. 296, No. 4 ( 2009-04), p. R1192-R1201
    Abstract: H + -ATPase-rich (HR) cells in zebrafish are known to be involved in acid secretion and Na + uptake mechanisms in zebrafish gills/skin; however, little is known about how HR cells are functionally regulated. In the present work, we studied the roles of Drosophila glial cell missing ( gcm), a cell fate-related transcription factor, in the differentiation and functional regulation of zebrafish HR cells. Zebrafish gcm2 ( zgcm2) was found to begin expression in zebrafish embryos at 10 h postfertilization (hpf), and to be extensively expressed in gills but only mildly so in eyes, heart, muscles, and testes. By whole mount in situ hybridization, zgcm2 mRNA signals were found in a group of cells on the zebrafish yolk sac surface initially in the tail bud stage (10 hpf); they had disappeared at 36 hpf and thereafter appeared again in the gill region from 48 hpf. Double fluorescence in situ hybridization further demonstrated specific colocalization of zgcm2 mRNA in HR cells in zebrafish embryos. Knockdown of zgcm2 with a specific morpholino oligonucleotide caused the complete disappearance of HR cells with a concomitant decrease in H + activity at the apical surface of HR cells, but it did not affect the occurrence of Na + -K + -ATPase-rich cells. A decrease in the H + -ATPase subunit A ( zatp6v1a) expression and no change in zgcm2 expression in zebrafish gills were seen from 12 h to 3 days after transfer to acidic fresh water, but a compensatory stimulation in the expressions of both genes appeared 4 days posttransfer. In conclusion, functional regulation of HR cells is probably achieved by enhancing cell differentiation via zGCM2 activation.
    Type of Medium: Online Resource
    ISSN: 0363-6119 , 1522-1490
    Language: English
    Publisher: American Physiological Society
    Publication Date: 2009
    detail.hit.zdb_id: 1477297-8
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  • 4
    Online Resource
    Online Resource
    eLife Sciences Publications, Ltd ; 2018
    In:  eLife Vol. 7 ( 2018-05-01)
    In: eLife, eLife Sciences Publications, Ltd, Vol. 7 ( 2018-05-01)
    Abstract: Many marine organisms such as mussels, sea urchins or corals, have skeletons and shells, which – due to their beautiful colors and shapes – are often desirable collector pieces. These structures are made from calcium and carbonate ions that react to form calcium carbonate crystals in a process known as biomineralization. In sea urchin larvae, for example, the skeleton is built by so-called primary mesenchyme cells, which work similar to the bone forming cells in mammals. These mesenchyme cells use calcium from the sea water, which travels to the site where the shell starts to form. About half of the carbonate comes from carbon dioxide that the animals make as they breathe, but it is not known how the other half gets to the site of biomineralization. Producing a skeleton generates acid, and marine animals need to be able to regulate their pH levels, as too acidic environments can dissolve the calcium carbonate and threatening to destroy the developing shell. How cells accumulate enough carbonate to make their shells, and how they cope with acidity is still poorly understood. Here, Hu et al. address this problem by studying purple sea urchin larvae, revealing that they use ion transporters to gather bicarbonate from seawater. These structures are part of a group of bicarbonate transporters known as the ‘SLC4 transporter family’, which sit across the membrane of the mesenchyme cells and move the bicarbonate ions along. As the sea urchin larvae develop, the levels of the transporter protein start to rise in mesenchyme cells, peaking around the time they are producing the skeleton. Stopping the production of the transporter hindered the larvae from building normal skeletons and also made their cells more acidic. It turns out that bicarbonate is more than a skeleton ingredient – it also helps to buffer the acid made in the process. Bicarbonate ions can combine with acidic molecules to form water and carbon dioxide. Bicarbonate pumped in from the sea neutralises the acidic molecules made during calcium carbonate formation, which helps to stabilize pH levels. When the acidity of the water was experimentally increased, it prompted the sea urchins to produce more of the SLC4 transporters, revealing that they may have another role to play. Their acid-neutralizing capability helped the animals to cope with changes in their environment. Taking on more bicarbonate could therefore help to compensate for rising acidity, allowing skeleton production to carry on as normal. This last finding is important in the context of ocean acidification. As the amount of carbon dioxide in the atmosphere increases, more of the gas dissolves in the sea. The chemical reactions that follow make the water more acidic and decreases the pH levels of the sea. Understanding how animals make their skeletons and shells, and manage acid, could reveal how they will cope as the environment changes in the future.
    Type of Medium: Online Resource
    ISSN: 2050-084X
    Language: English
    Publisher: eLife Sciences Publications, Ltd
    Publication Date: 2018
    detail.hit.zdb_id: 2687154-3
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  • 5
    Online Resource
    Online Resource
    American Physiological Society ; 2009
    In:  American Journal of Physiology-Regulatory, Integrative and Comparative Physiology Vol. 296, No. 5 ( 2009-05), p. R1650-R1660
    In: American Journal of Physiology-Regulatory, Integrative and Comparative Physiology, American Physiological Society, Vol. 296, No. 5 ( 2009-05), p. R1650-R1660
    Abstract: The thiazide-sensitive Na + -Cl − cotransporter (NCC), a member of the SLC12 family, is mainly expressed in the apical membrane of the mammalian distal convoluted tubule (DCT) cells, is responsible for cotransporting Na + and Cl − from the lumen into DCT cells and plays a major role in the mammalian renal NaCl reabsorption. The NCC has also been reported in fish, but the functional role in fish ion regulation is yet unclear. The present study used zebrafish as an in vivo model to test the hypothesis of whether the NCC plays a role in Na + and/or Cl − uptake mechanisms. Four NCCs were cloned, and only one of them, zebrafish (z) slc12a10.2 was found to predominately and specifically be expressed in gills. Double in situ hybridization/immunocytochemistry in zebrafish skin/gills demonstrated that the specific expression of zslc12a10.2 mRNA in a novel group of ionocytes differed from those of the previously-reported H + -ATPase-rich (HR) cells and Na + -K + -ATPase-rich (NaR) cells. Gill mRNA expression of zslc12a10.2 was induced by a low-Cl environment that stimulated fish Cl − influx, while a low-Na environment suppressed this expression. Incubation with metolazone, a specific inhibitor of the NCC, impaired both Na + and Cl − influx in 5-day postfertilization (dpf) zebrafish embryos. Translational knockdown of zslc12a10.2 with a specific morpholino caused significant decreases in both Cl − influx and Cl − content of 5-dpf zebrafish embryos, suggesting that the operation of zNCC-like 2 results in a net uptake of Cl − in zebrafish. On the contrary, zslc12a10.2 morphants showed increased Na + influx and content that resulted from upregulation of mRNA expressions of Na + -H + exchanger 3b and carbonic anhydrase 15a in HR cells. These results for the first time provide in vivo molecular physiological evidence for the possible role of the NCC in the Cl − uptake mechanism in zebrafish skin/gills.
    Type of Medium: Online Resource
    ISSN: 0363-6119 , 1522-1490
    Language: English
    Publisher: American Physiological Society
    Publication Date: 2009
    detail.hit.zdb_id: 1477297-8
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  • 6
    Online Resource
    Online Resource
    Frontiers Media SA ; 2023
    In:  Frontiers in Marine Science Vol. 10 ( 2023-1-20)
    In: Frontiers in Marine Science, Frontiers Media SA, Vol. 10 ( 2023-1-20)
    Abstract: How teleosts take up Na + from the surrounding freshwater (FW) as well as the underlying mechanisms associated with this process have received considerable attention over the past 85 years. Owing to an enormous ion gradient between hypotonic FW and fish body fluids, teleosts gills have to actively absorb Na + (via ionocytes) to compensate for the passive loss of Na + . To date, three models have been proposed for Na + uptake in teleost ionocytes, including Na + /H + exchanger (NHE)-mediated, acid-sensing ion channel (ASIC)-mediated, Na + -Cl - co-transporter (NCC)-mediated pathways. However, some debates regarding these models and unclear mechanisms still remain. To better understand how teleosts take up Na + from FW, this mini-review summarizes the main progress and related regulatory mechanisms of Na + uptake, and discusses some of the challenges to the current models.
    Type of Medium: Online Resource
    ISSN: 2296-7745
    Language: Unknown
    Publisher: Frontiers Media SA
    Publication Date: 2023
    detail.hit.zdb_id: 2757748-X
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  • 7
    Online Resource
    Online Resource
    Bioscientifica ; 2021
    In:  Journal of Endocrinology Vol. 251, No. 2 ( 2021-11-01), p. 149-159
    In: Journal of Endocrinology, Bioscientifica, Vol. 251, No. 2 ( 2021-11-01), p. 149-159
    Abstract: Estrogen-related receptors (ERRs) are known to function in mammalian kidney as key regulators of ion transport-related genes; however, a comprehensive understanding of the physiological functions of ERRs in vertebrate body fluid ionic homeostasis is still elusive. Here, we used medaka ( Oryzias melastigma ), a euryhaline teleost, to investigate how ERRs are involved in ion regulation. After transferring medaka from hypertonic seawater to hypotonic freshwater (FW), the mRNA expression levels of errγ2 were highly upregulated, suggesting that Errγ2 may play a crucial role in ion uptake. In situ hybridization showed that errγ2 was specifically expressed in ionocytes, the cells responsible for Na + /Cl − transport. In normal FW, ERRγ2 morpholino knockdown caused reductions in the mRNA expression of Na + /Cl − cotransporter (Ncc), the number of Ncc ionocytes, Na + /Cl − influxes of ionocytes, and whole-body Na + /Cl − contents. In FW with low Na + and low Cl − , the expression levels of mRNA for Na + /H + exchanger 3 (Nhe3) and Ncc were both decreased in Errγ2 morphants. Treating embryos with DY131, an agonist of Errγ, increased the whole-body Na + /Cl − contents and ncc mRNA expression in Errγ2 morphants. As such, medaka Errγ2 may control Na + /Cl − uptake by regulating ncc and/or nhe3 mRNA expression and ionocyte number, and these regulatory actions may be subtly adjusted depending on internal and external ion concentrations. These findings not only provide new insights into the underpinning mechanism of actions of ERRs, but also enhance our understanding of their roles in body fluid ionic homeostasis for adaptation to changing environments during vertebrate evolution.
    Type of Medium: Online Resource
    ISSN: 0022-0795 , 1479-6805
    Language: Unknown
    Publisher: Bioscientifica
    Publication Date: 2021
    detail.hit.zdb_id: 1474892-7
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  • 8
    Online Resource
    Online Resource
    Ivyspring International Publisher ; 2015
    In:  International Journal of Biological Sciences Vol. 11, No. 10 ( 2015), p. 1190-1203
    In: International Journal of Biological Sciences, Ivyspring International Publisher, Vol. 11, No. 10 ( 2015), p. 1190-1203
    Type of Medium: Online Resource
    ISSN: 1449-2288
    Language: English
    Publisher: Ivyspring International Publisher
    Publication Date: 2015
    detail.hit.zdb_id: 2179208-2
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  • 9
    In: Journal of Cell Science, The Company of Biologists, Vol. 127, No. 19 ( 2014-10-01), p. e1-e1
    Type of Medium: Online Resource
    ISSN: 1477-9137 , 0021-9533
    Language: English
    Publisher: The Company of Biologists
    Publication Date: 2014
    detail.hit.zdb_id: 219171-4
    detail.hit.zdb_id: 1483099-1
    SSG: 12
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  • 10
    In: International Journal of Molecular Sciences, MDPI AG, Vol. 24, No. 7 ( 2023-04-01), p. 6597-
    Abstract: The gills are the major organ for Na+ uptake in teleosts. It was proposed that freshwater (FW) teleosts adopt Na+/H+ exchanger 3 (Nhe3) as the primary transporter for Na+ uptake and Na+-Cl− co-transporter (Ncc) as the backup transporter. However, convincing molecular physiological evidence to support the role of Ncc in branchial Na+ uptake is still lacking due to the limitations of functional assays in the gills. Thus, this study aimed to reveal the role of branchial Ncc in Na+ uptake with an in vivo detection platform (scanning ion-selective electrode technique, SIET) that has been recently established in fish gills. First, we identified that Ncc2-expressing cells in zebrafish gills are a specific subtype of ionocyte (NCC ionocytes) by using single-cell transcriptome analysis and immunofluorescence. After a long-term low-Na+ FW exposure, zebrafish increased branchial Ncc2 expression and the number of NCC ionocytes and enhanced gill Na+ uptake capacity. Pharmacological treatments further suggested that Na+ is indeed taken up by Ncc, in addition to Nhe, in the gills. These findings reveal the uptake roles of both branchial Ncc and Nhe under FW and shed light on osmoregulatory physiology in adult fish.
    Type of Medium: Online Resource
    ISSN: 1422-0067
    Language: English
    Publisher: MDPI AG
    Publication Date: 2023
    detail.hit.zdb_id: 2019364-6
    SSG: 12
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