Abstract

Cation-chloride cotransporters, such as the Na(+)/K(+)/2Cl(-) cotransporter (NKCC) and Na(+)/Cl(-) cotransporter (NCC), are localized to the apical or basolateral plasma membranes of epithelial cells and are involved in active ion absorption or secretion. The objectives of this study were to clone and identify ;freshwater-type' and ;seawater-type' cation-chloride cotransporters of euryhaline Mozambique tilapia (Oreochromis mossambicus) and to determine their intracellular localization patterns within mitochondria-rich cells (MRCs). From tilapia gills, we cloned four full-length cDNAs homologous to human cation-chloride cotransporters and designated them as tilapia NKCC1a, NKCC1b, NKCC2 and NCC. Out of the four candidates, the mRNA encoding NKCC1a was highly expressed in the yolk-sac membrane and gills (sites of the MRC localization) of seawater-acclimatized fish, whereas the mRNA encoding NCC was exclusively expressed in the yolk-sac membrane and gills of freshwater-acclimatized fish. We then generated antibodies specific for tilapia NKCC1a and NCC and conducted whole-mount immunofluorescence staining for NKCC1a and NCC, together with Na(+)/K(+)-ATPase, cystic fibrosis transmembrane conductance regulator (CFTR) and Na(+)/H(+) exchanger 3 (NHE3), on the yolk-sac membrane of tilapia embryos acclimatized to freshwater or seawater. The simultaneous quintuple-color immunofluorescence staining allowed us to classify MRCs clearly into four types: types I, II, III and IV. The NKCC1a immunoreactivity was localized to the basolateral membrane of seawater-specific type-IV MRCs, whereas the NCC immunoreactivity was restricted to the apical membrane of freshwater-specific type-II MRCs. Taking account of these data at the level of both mRNA and protein, we deduce that NKCC1a is the seawater-type cotransporter involved in ion secretion by type-IV MRCs and that NCC is the freshwater-type cotransporter involved in ion absorption by type-II MRCs. We propose a novel ion-uptake model by MRCs in freshwater that incorporates apically located NCC. We also reevaluate a traditional ion-uptake model incorporating NHE3; the mRNA was highly expressed in freshwater, and the immunoreactivity was found at the apical membrane of other freshwater-specific MRCs.

Highlights

  • Euryhaline teleost fish, such as Mozambique tilapia, Oreochromis mossambicus, are able to live in waters with a wide range of salinity and maintain nearly constant ion concentrations of body fluids irrespective of the external salinity

  • Four cation–chloride cotransporters isolated from tilapia gills From the gills of Mozambique tilapia, three full-length cDNAs homologous to human Na+/K+/2Cl– cotransporter (NKCC) were obtained by the PCR-based strategy, and one full-length cDNA homologous to human Na+/Cl– cotransporter (NCC) rather than NKCC was isolated by immunoscreening using antibody against human NKCC1

  • These four cDNAs exhibited open reading frames encoding proteins of 1001 to 1151 amino acids (Fig. 2). The former three NKCC homologs were designated as tilapia NKCC1a

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Summary

Introduction

Euryhaline teleost fish, such as Mozambique tilapia, Oreochromis mossambicus, are able to live in waters with a wide range of salinity and maintain nearly constant ion concentrations of body fluids irrespective of the external salinity. Numerous studies on euryhaline teleosts demonstrate that specialized mitochondria-rich cells (MRCs, referred to as chloride cells or ionocytes) in the gill epithelium regulate the internal ionic composition, either by secreting excess internal ions in seawater or by taking up needed ions in freshwater (for a review, see Evans et al, 2005). Particular epithelial cells (including fish MRCs) transport ions from the internal to the external environments (i.e. secretion) or from the external to the internal environments (absorption). This vectorial ion transport is performed by combinations of several ion pumps, transporters and channels selectively expressed in each of the apical and basolateral membranes (Jentsch et al, 2004). Determining the localization patterns of the ion-transport proteins at the apical and basolateral membranes will be essential for determining the ion-transport functions of the cells

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