Identification of Zebrafish Fxyd11a Protein that is Highly Expressed in Ion-Transporting Epithelium of the Gill and Skin and its Possible Role in Ion Homeostasis

FXYD proteins, small single-transmembrane proteins, have been proposed to be auxiliary regulatory subunits of Na+–K+-ATPase and have recently been implied in ion osmoregulation of teleost fish. In freshwater (FW) fish, numerous ions are actively taken up through mitochondrion-rich cells (MRCs) of the gill and skin epithelia, using the Na+ electrochemical gradient generated by Na+–K+-ATPase. In the present study, to understand the molecular mechanism for the regulation of Na+–K+-ATPase in MRCs of FW fish, we sought to identify FXYD proteins expressed in MRCs of zebrafish. Reverse-transcriptase PCR studies of adult zebrafish tissues revealed that, out of eight fxyd genes found in zebrafish database, only zebrafish fxyd11 (zfxyd11) mRNA exhibited a gill-specific expression. Double immunofluorescence staining showed that zFxyd11 is abundantly expressed in MRCs rich in Na+–K+-ATPase (NaK-MRCs) but not in those rich in vacuolar-type H+-transporting ATPase. An in situ proximity ligation assay demonstrated its close association with Na+–K+-ATPase in NaK-MRCs. The zfxyd11 mRNA expression was detectable at 1 day postfertilization, and its expression levels in the whole larvae and adult gills were regulated in response to changes in environmental ionic concentrations. Furthermore, knockdown of zFxyd11 resulted in a significant increase in the number of Na+–K+-ATPase–positive cells in the larval skin. These results suggest that zFxyd11 may regulate the transport ability of NaK-MRCs by modulating Na+–K+-ATPase activity, and may be involved in the regulation of body fluid and electrolyte homeostasis.

[1]  M. Ekker,et al.  The involvement of SLC26 anion transporters in chloride uptake in zebrafish (Danio rerio) larvae , 2009, Journal of Experimental Biology.

[2]  S. Perry,et al.  Evidence that SLC26 anion transporters mediate branchial chloride uptake in adult zebrafish (Danio rerio). , 2009, American journal of physiology. Regulatory, integrative and comparative physiology.

[3]  P. Hwang Ion uptake and acid secretion in zebrafish (Danio rerio) , 2009, Journal of Experimental Biology.

[4]  Bo-Kai Liao,et al.  Expression regulation of Na+-K+-ATPase alpha1-subunit subtypes in zebrafish gill ionocytes. , 2009, American journal of physiology. Regulatory, integrative and comparative physiology.

[5]  C. Toyoshima,et al.  Crystal structure of the sodium–potassium pump at 2.4 Å resolution , 2009, Nature.

[6]  K. Kawakami,et al.  Mechanism of development of ionocytes rich in vacuolar-type H(+)-ATPase in the skin of zebrafish larvae. , 2009, Developmental biology.

[7]  P. Hwang,et al.  Role of SLC12A10.2, a Na-Cl cotransporter-like protein, in a Cl uptake mechanism in zebrafish (Danio rerio). , 2009, American journal of physiology. Regulatory, integrative and comparative physiology.

[8]  T. Kaneko,et al.  Effects of stanniocalcin 1 on calcium uptake in zebrafish (Danio rerio) embryo. , 2009, American journal of physiology. Regulatory, integrative and comparative physiology.

[9]  Tsung-Han Lee,et al.  Branchial FXYD protein expression in response to salinity change and its interaction with Na+/K+-ATPase of the euryhaline teleost Tetraodon nigroviridis , 2008, Journal of Experimental Biology.

[10]  P. Hwang,et al.  Functional regulation of H+-ATPase-rich cells in zebrafish embryos acclimated to an acidic environment. , 2009, American journal of physiology. Cell physiology.

[11]  U. Landegren,et al.  Characterizing proteins and their interactions in cells and tissues using the in situ proximity ligation assay. , 2008, Methods.

[12]  Bo-Kai Liao,et al.  Carbonic anhydrase 2-like a and 15a are involved in acid-base regulation and Na+ uptake in zebrafish H+-ATPase-rich cells. , 2008, American journal of physiology. Cell physiology.

[13]  N. Nakamura,et al.  Regulation of mitochondrial morphology by USP30, a deubiquitinating enzyme present in the mitochondrial outer membrane. , 2008, Molecular biology of the cell.

[14]  C. Tipsmark Identification of FXYD protein genes in a teleost: tissue-specific expression and response to salinity change. , 2008, American journal of physiology. Regulatory, integrative and comparative physiology.

[15]  P. Nissen,et al.  Crystal structure of the sodium–potassium pump , 2007, Nature.

[16]  Bo-Kai Liao,et al.  Expression and water calcium dependence of calcium transporter isoforms in zebrafish gill mitochondrion-rich cells , 2007, BMC Genomics.

[17]  T. Kaneko,et al.  Gene expression of Na+/H+ exchanger in zebrafish H+ -ATPase-rich cells during acclimation to low-Na+ and acidic environments. , 2007, American journal of physiology. Cell physiology.

[18]  K. Kawakami,et al.  Localization of ammonia transporter Rhcg1 in mitochondrion-rich cells of yolk sac, gill, and kidney of zebrafish and its ionic strength-dependent expression. , 2007, American journal of physiology. Regulatory, integrative and comparative physiology.

[19]  M. Hammerschmidt,et al.  Foxi3 transcription factors and Notch signaling control the formation of skin ionocytes from epidermal precursors of the zebrafish embryo. , 2007, Developmental biology.

[20]  P. M. Craig,et al.  Gill membrane remodeling with soft-water acclimation in zebrafish (Danio rerio). , 2007, Physiological genomics.

[21]  S. Hirose,et al.  Expression of endocrine genes in zebrafish larvae in response to environmental salinity. , 2007, The Journal of endocrinology.

[22]  T. Kaneko,et al.  Knockdown of V-ATPase subunit A (atp6v1a) impairs acid secretion and ion balance in zebrafish (Danio rerio). , 2007, American journal of physiology. Regulatory, integrative and comparative physiology.

[23]  Yun-Jin Jiang,et al.  A Positive Regulatory Loop between foxi3a and foxi3b Is Essential for Specification and Differentiation of Zebrafish Epidermal Ionocytes , 2007, PloS one.

[24]  Jean-Luc Puel,et al.  FXYD6 Is a Novel Regulator of Na,K-ATPase Expressed in the Inner Ear* , 2007, Journal of Biological Chemistry.

[25]  K. Geering,et al.  Structural and Functional Properties of Two Human FXYD3 (Mat-8) Isoforms* , 2006, Journal of Biological Chemistry.

[26]  L. Burcea,et al.  Cytoplasmic targeting signals mediate delivery of phospholemman to the plasma membrane. , 2006, American journal of physiology. Cell physiology.

[27]  S. Hirose,et al.  Spliced isoforms of LIM‐domain‐binding protein (CLIM/NLI/Ldb) lacking LIM interaction domain , 2006, Journal of biochemistry.

[28]  K. Geering FXYD proteins: new regulators of Na-K-ATPase. , 2006, American journal of physiology. Renal physiology.

[29]  J. Kunkel,et al.  Proton pump-rich cell secretes acid in skin of zebrafish larvae. , 2006, American journal of physiology. Cell physiology.

[30]  Bo-Kai Liao,et al.  Epithelial Ca(2+) channel expression and Ca(2+) uptake in developing zebrafish. , 2005, American journal of physiology. Regulatory, integrative and comparative physiology.

[31]  K. Geering,et al.  FXYD3 (Mat-8), a new regulator of Na,K-ATPase. , 2005, Molecular biology of the cell.

[32]  N. Nakamura,et al.  MARCH-II is a syntaxin-6-binding protein involved in endosomal trafficking. , 2005, Molecular biology of the cell.

[33]  Rebecca J Blatt,et al.  Hypertrophy, increased ejection fraction, and reduced Na-K-ATPase activity in phospholemman-deficient mice. , 2005, American journal of physiology. Heart and circulatory physiology.

[34]  L. B. Kirschner The mechanism of sodium chloride uptake in hyperregulating aquatic animals , 2004, Journal of Experimental Biology.

[35]  A. Tucker,et al.  Effects of phospholemman downregulation on contractility and [Ca(2+)]i transients in adult rat cardiac myocytes. , 2004, American journal of physiology. Heart and circulatory physiology.

[36]  F. Grahammer,et al.  Cellular Physiology Cellular Physiology Cellular Physiology Cellular Physiology Cellular Physiology and Biochemistr and Biochemistr and Biochemistr and Biochemistr and Biochemistryyyyy Kidney and Colon Electrolyte Transport in CHIF Knockout Mice , 2022 .

[37]  Y. Takei,et al.  Molecular biology of major components of chloride cells. , 2003, Comparative biochemistry and physiology. Part B, Biochemistry & molecular biology.

[38]  S. Perry,et al.  Channels, pumps, and exchangers in the gill and kidney of freshwater fishes: their role in ionic and acid-base regulation. , 2003, Journal of experimental zoology. Part A, Comparative experimental biology.

[39]  M. Romero,et al.  Mechanism of acid adaptation of a fish living in a pH 3.5 lake. , 2003, American journal of physiology. Regulatory, integrative and comparative physiology.

[40]  M. Kashiwagi,et al.  RING finger, B-box, and coiled-coil (RBCC) protein expression in branchial epithelial cells of Japanese eel, Anguilla japonica. , 2002, European journal of biochemistry.

[41]  N. Farman,et al.  A functional interaction between CHIF and Na-K-ATPase: implication for regulation by FXYD proteins. , 2002, American journal of physiology. Renal physiology.

[42]  H. Garty,et al.  Generation and phenotypic analysis of CHIF knockout mice. , 2002, American journal of physiology. Renal physiology.

[43]  K. Geering,et al.  Phospholemman (FXYD1) associates with Na,K-ATPase and regulates its transport properties , 2002, Proceedings of the National Academy of Sciences of the United States of America.

[44]  W. Marshall,et al.  Na(+), Cl(-), Ca(2+) and Zn(2+) transport by fish gills: retrospective review and prospective synthesis. , 2002, The Journal of experimental zoology.

[45]  K. Geering,et al.  FXYD7 is a brain‐specific regulator of Na,K‐ATPase α1–β isozymes , 2002 .

[46]  R. Blostein,et al.  Distinct Regulatory Effects of the Na,K-ATPase γ Subunit* , 2002, The Journal of Biological Chemistry.

[47]  K. Geering,et al.  CHIF, a member of the FXYD protein family, is a regulator of Na,K‐ATPase distinct from the γ‐subunit , 2001, The EMBO journal.

[48]  N. Farman,et al.  Functional Role and Immunocytochemical Localization of the γa and γb Forms of the Na,K-ATPase γ Subunit* , 2001, The Journal of Biological Chemistry.

[49]  H. Vorum,et al.  Identification of a Phospholemman-like Protein from Shark Rectal Glands , 2000, The Journal of Biological Chemistry.

[50]  H. Bokhoven,et al.  Dominant isolated renal magnesium loss is caused by misrouting of the Na+,K+-ATPase γ-subunit , 2000, Nature Genetics.

[51]  E. Rael,et al.  The FXYD gene family of small ion transport regulators or channels: cDNA sequence, protein signature sequence, and expression. , 2000, Genomics.

[52]  K. Sweadner,et al.  The γ Subunit Modulates Na+ and K+Affinity of the Renal Na,K-ATPase* , 1999, The Journal of Biological Chemistry.

[53]  Y. Suzuki,et al.  Inwardly rectifying K+ channel Kir7.1 is highly expressed in thyroid follicular cells, intestinal epithelial cells and choroid plexus epithelial cells: implication for a functional coupling with Na+,K+-ATPase. , 1999, The Biochemical journal.

[54]  B. Tang,et al.  A 29-Kilodalton Golgi SolubleN-Ethylmaleimide-sensitive Factor Attachment Protein Receptor (Vti1-rp2) Implicated in Protein Trafficking in the Secretory Pathway* , 1998, The Journal of Biological Chemistry.

[55]  M. McNiven,et al.  A Novel Dynamin-like Protein Associates with Cytoplasmic Vesicles and Tubules of the Endoplasmic Reticulum in Mammalian Cells , 1998, The Journal of cell biology.

[56]  K. Geering,et al.  The γ subunit is a specific component of the Na,K‐ATPase and modulates its transport function , 1997, The EMBO journal.

[57]  S. McCormick Fluorescent labelling of Na+,K+-ATPase in intact cells by use of a fluorescent derivative of ouabain: Salinity and teleost chloride cells , 1990, Cell and Tissue Research.

[58]  S. Perry,et al.  Evidence that SLC26 anion transporters mediate branchial chloride uptake in adult zebrafish (Danio rerio). , 2009, American journal of physiology. Regulatory, integrative and comparative physiology.

[59]  K. Kawakami,et al.  Visualization in zebrafish larvae of Na(+) uptake in mitochondria-rich cells whose differentiation is dependent on foxi3a. , 2007, American journal of physiology. Regulatory, integrative and comparative physiology.

[60]  R. Heaney,et al.  Calcium absorption , 2007, Calcified Tissue International.

[61]  B. Nilius,et al.  Calcium absorption across epithelia. , 2005, Physiological reviews.

[62]  K. Choe,et al.  The multifunctional fish gill: dominant site of gas exchange, osmoregulation, acid-base regulation, and excretion of nitrogenous waste. , 2005, Physiological reviews.

[63]  Xueqian Zhang,et al.  Phospholemman modulates Na+/Ca2+ exchange in adult rat cardiac myocytes. , 2003, American journal of physiology. Heart and circulatory physiology.

[64]  K. Geering,et al.  FXYD7 is a brain-specific regulator of Na,K-ATPase alpha 1-beta isozymes. , 2002, The EMBO journal.

[65]  K. Geering The functional role of beta subunits in oligomeric P-type ATPases. , 2001, Journal of bioenergetics and biomembranes.

[66]  A. Doucet,et al.  Sodium-potassium-adenosinetriphosphatase-dependent sodium transport in the kidney: hormonal control. , 2001, Physiological reviews.

[67]  M. Westerfield The zebrafish book : a guide for the laboratory use of zebrafish (Danio rerio) , 1995 .