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Expression regulation of Na + -K + -ATPase α1-subunit subtypes in zebrafish gill ionocytes

In zebrafish ( Danio rerio), six distinct Na + -K + -ATPase (NKA) α1-subunit genes have been identified, and four of them, zatp1a1a.1, zatp1a1a.2, zatp1a1a.4, and zatp1a1a.5, are expressed in embryonic skin where different types of ionocytes appear. The present study attempted to test a hypothesis o...

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Published in:American journal of physiology. Regulatory, integrative and comparative physiology integrative and comparative physiology, 2009-06, Vol.296 (6), p.R1897-R1906
Main Authors: Liao, Bo-Kai, Chen, Ruo-Dong, Hwang, Pung-Pung
Format: Article
Language:English
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Summary:In zebrafish ( Danio rerio), six distinct Na + -K + -ATPase (NKA) α1-subunit genes have been identified, and four of them, zatp1a1a.1, zatp1a1a.2, zatp1a1a.4, and zatp1a1a.5, are expressed in embryonic skin where different types of ionocytes appear. The present study attempted to test a hypothesis of whether these NKA α1 paralogues are specifically expressed and function in respective ionocytes. Double fluorescence in situ hybridization analysis demonstrated the specific expression of zatp1a1a.1, zatp1a1a.2, and zatp1a1a. 5 in NKA-rich (NaR) cells, Na + -Cl − cotransporter (NCC)-expressing cells, and H + -ATPase-rich (HR) cells, respectively, based on the colocalization of the three NKA α1 genes with marker genes of the respective ionocytes (epithelial Ca 2+ channel in NaR cells; NCC in NCC cells; and H + -ATPase and Na + /H + exchanger 3b in HR cells). The mRNA expression (by real-time PCR) of zatp1a1a.1, zatp1a1a.2, and zatp1a1a.5 were, respectively, upregulated by low-Ca 2+ , low-Cl − , and low-Na + freshwater, which had previously been reported to stimulate uptake functions of Ca 2+ , Cl − , and Na + . However, zatp1a1a.4 was not colocalized with any of the three types of ionocytes, nor did its mRNA respond to the ambient ions examined. Taken together, zATP1a1a.1, zATP1a1a.2, and zATP1a1a.5 may provide driving force for Na + -coupled cotransporter activity specifically in NaR, NCC, and HR cells, respectively.
ISSN:0363-6119
1522-1490
DOI:10.1152/ajpregu.00029.2009