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Sulfate transporters involved in sulfate secretion in the kidney are localized in the renal proximal tubule II of the elephant fish (Callorhinchus milii).

Authors :
Kumi Hasegawa
Akira Kato
Taro Watanabe
Wataru Takagi
Romero, Michael F.
Bell, Justin D.
Toop, Tes
Donald, John A.
Susumu Hyodo
Source :
American Journal of Physiology: Regulatory, Integrative & Comparative Physiology; Jul2016, Vol. 311 Issue 1, pR66-R78, 13p
Publication Year :
2016

Abstract

Most vertebrates, including cartilaginous fishes, maintain their plasma SO<subscript>4</subscript><superscript>2-</superscript> concentration ([SO<subscript>4</subscript><superscript>2-</superscript>]) within a narrow range of 0.2-1 mM. As seawater has a [SO<subscript>4</subscript><superscript>2-</superscript>] about 40 times higher than that of the plasma, SO<subscript>4</subscript><superscript>2-</superscript> excretion is the major role of kidneys in marine teleost fishes. It has been suggested that cartilaginous fishes also excrete excess SO<subscript>4</subscript><superscript>2-</superscript> via the kidney. However, little is known about the underlying mechanisms for SO<subscript>4</subscript><superscript>2-</superscript> 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 SO<subscript>4</subscript><superscript>2-</superscript> 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 SO<subscript>4</subscript><superscript>2-</superscript> transporter, while cmSlc26a6 is an apically located, electrogenic Cl<superscript>-</superscript>/SO<subscript>4</subscript><superscript>2-</superscript> exchanger. In addition, we found that both cmSlc26a1 and cmSlc26a6 were abundantly expressed in the kidney of embryos; SO<subscript>4</subscript><superscript>2-</superscript> 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 SO<subscript>4</subscript><superscript>2-</superscript> by the kidney of elephant fish. Possible mechanisms for SO<subscript>4</subscript><superscript>2-</superscript> secretion in the PII segment are discussed. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
03636119
Volume :
311
Issue :
1
Database :
Complementary Index
Journal :
American Journal of Physiology: Regulatory, Integrative & Comparative Physiology
Publication Type :
Academic Journal
Accession number :
116602678
Full Text :
https://doi.org/10.1152/ajpregu.00477.2015