» Articles » PMID: 27122370

Sulfate Transporters Involved in Sulfate Secretion in the Kidney Are Localized in the Renal Proximal Tubule II of the Elephant Fish (Callorhinchus Milii)

Overview
Specialty Physiology
Date 2016 Apr 29
PMID 27122370
Citations 6
Authors
Affiliations
Soon will be listed here.
Abstract

Most vertebrates, including cartilaginous fishes, maintain their plasma SO4 (2-) concentration ([SO4 (2-)]) within a narrow range of 0.2-1 mM. As seawater has a [SO4 (2-)] about 40 times higher than that of the plasma, SO4 (2-) excretion is the major role of kidneys in marine teleost fishes. It has been suggested that cartilaginous fishes also excrete excess SO4 (2-) via the kidney. However, little is known about the underlying mechanisms for SO4 (2-) transport in cartilaginous fish, largely due to the extraordinarily elaborate four-loop configuration of the nephron, which consists of at least 10 morphologically distinguishable segments. In the present study, we determined cDNA sequences from the kidney of holocephalan elephant fish (Callorhinchus milii) that encoded solute carrier family 26 member 1 (Slc26a1) and member 6 (Slc26a6), which are SO4 (2-) transporters that are expressed in mammalian and teleost kidneys. Elephant fish Slc26a1 (cmSlc26a1) and cmSlc26a6 mRNAs were coexpressed in the proximal II (PII) segment of the nephron, which comprises the second loop in the sinus zone. Functional analyses using Xenopus oocytes and the results of immunohistochemistry revealed that cmSlc26a1 is a basolaterally located electroneutral SO4 (2-) transporter, while cmSlc26a6 is an apically located, electrogenic Cl(-)/SO4 (2-) exchanger. In addition, we found that both cmSlc26a1 and cmSlc26a6 were abundantly expressed in the kidney of embryos; SO4 (2-) was concentrated in a bladder-like structure of elephant fish embryos. Our results demonstrated that the PII segment of the nephron contributes to the secretion of excess SO4 (2-) by the kidney of elephant fish. Possible mechanisms for SO4 (2-) secretion in the PII segment are discussed.

Citing Articles

In vitro and in vivo gene transfer in the cloudy catshark Scyliorhinus torazame.

Fujimori C, Umatani C, Chimura M, Ijiri S, Bando H, Hyodo S Dev Growth Differ. 2022; 64(9):558-565.

PMID: 36376176 PMC: 10099843. DOI: 10.1111/dgd.12824.


Molecular and morphological investigations on the renal mechanisms enabling euryhalinity of red stingray .

Aburatani N, Takagi W, Wong M, Kuraku S, Tanegashima C, Kadota M Front Physiol. 2022; 13:953665.

PMID: 36017340 PMC: 9396271. DOI: 10.3389/fphys.2022.953665.


Membrane Transport Proteins Expressed in the Renal Tubular Epithelial Cells of Seawater and Freshwater Teleost Fishes.

Kato A, Nagashima A, Hosono K, Romero M Front Physiol. 2022; 13:939114.

PMID: 35812342 PMC: 9259948. DOI: 10.3389/fphys.2022.939114.


Ion Transporters and Osmoregulation in the Kidney of Teleost Fishes as a Function of Salinity.

Takvam M, Wood C, Kryvi H, Nilsen T Front Physiol. 2021; 12:664588.

PMID: 33967835 PMC: 8098666. DOI: 10.3389/fphys.2021.664588.


Absence of the sulfate transporter SAT-1 has no impact on oxalate handling by mouse intestine and does not cause hyperoxaluria or hyperoxalemia.

Whittamore J, Stephens C, Hatch M Am J Physiol Gastrointest Liver Physiol. 2018; 316(1):G82-G94.

PMID: 30383413 PMC: 6383384. DOI: 10.1152/ajpgi.00299.2018.


References
1.
Pritchard J, Renfro J . Renal sulfate transport at the basolateral membrane is mediated by anion exchange. Proc Natl Acad Sci U S A. 1983; 80(9):2603-7. PMC: 393875. DOI: 10.1073/pnas.80.9.2603. View

2.
Beyenbach K, Petzel D, Cliff W . Renal proximal tubule of flounder. I. Physiological properties. Am J Physiol. 1986; 250(4 Pt 2):R608-15. DOI: 10.1152/ajpregu.1986.250.4.R608. View

3.
Xie Q, Welch R, Mercado A, Romero M, Mount D . Molecular characterization of the murine Slc26a6 anion exchanger: functional comparison with Slc26a1. Am J Physiol Renal Physiol. 2002; 283(4):F826-38. DOI: 10.1152/ajprenal.00079.2002. View

4.
Jones P, Binns D, Chang H, Fraser M, Li W, McAnulla C . InterProScan 5: genome-scale protein function classification. Bioinformatics. 2014; 30(9):1236-40. PMC: 3998142. DOI: 10.1093/bioinformatics/btu031. View

5.
Takabe S, Teranishi K, Takaki S, Kusakabe M, Hirose S, Kaneko T . Morphological and functional characterization of a novel Na+/K+-ATPase-immunoreactive, follicle-like structure on the gill septum of Japanese banded houndshark, Triakis scyllium. Cell Tissue Res. 2012; 348(1):141-53. DOI: 10.1007/s00441-012-1344-5. View