Evidence that SLC26 anion transporters mediate branchial chloride uptake in adult zebrafish (Danio rerio)

Experiments were performed to test the hypothesis that three members of the SLC26 anion transporter gene family (SLC26a3, A4, and A6; hereafter termed za3, za4, and za6) mediate branchial [Cl.sup.-]/[HCO.sup.-.sub.3] exchange in adult zebrafish (Danio rerio). Real-time RT-PCR demonstrated that the gill expressed relatively high levels of za6 mRNA; za3 and za4 mRNA, while present, were less abundant. Also, za4 and za6 were expressed at relatively high levels in the kidney. The results of in situ hybridization or immunocytochemistry (za3 only) experiments performed on gill sections revealed that the SLC26 transporters were predominantly expressed on the filament epithelium (especially within the interlamellar regions) and to a lesser extent on the lamellar epithelium at the base of lamellae. This distribution pattern suggests that the SLC26 anion transporters are localized to mitochondrion-rich cells (ionocytes). Transferring fish to water containing low [[Cl.sup.-]] (0.02 mmol/l) resulted in significant increases in branchial SLC26 mRNA expression after 5-10 days of exposure relative to fish raised in normal water [[Cl.sup.-]] (0.4 mmol/l); transferring fish to [Cl.sup.-]-enriched water (2.0 mmol/l) was without effect on mRNA levels. Transferring fish to water containing elevated levels of NaHC[O.sub.3] (10-12.5 mmol/l) caused marked increases in branchial SLC26 mRNA expression between 3 and l0 days of transfer that was associated with a significant 40% increase in [Cl.sup.-]-uptake (as measured upon return to normal water after 7 days). A decrease in whole body net acid excretion (equivalent to an increase in net base excretion) in fish previously maintained in high [NaHC[O.sub.3]] water, concurrent with increases in [Cl.sup.-] uptake and SLC26 mRNA levels, suggests a role for these anion transporters in [Cl.sup.-] uptake and acid-base regulation owing to their [Cl.sup.-]/HC[O.sup.-.sub.3] exchange activities. SLC26a3; SLC26a4; SLC26a6; pendrin; ionic regulation; acid-base balance; mitochondrion rich cell; gill doi: 10.1152/ajpregu.00327.2009.