4.3 Article

Na+/HCO3- cotransporter 1 (nbce 1) isoform gene expression during smoltification and seawater acclimation of Atlantic salmon

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SPRINGER HEIDELBERG
DOI: 10.1007/s00360-022-01443-8

关键词

Gill; Intestine; Ionocyte; Parr; Pyloric caeca; Smolts

资金

  1. National Science Foundation [IOS-1755131]

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The life history of Atlantic salmon involves a migration from freshwater to marine environments, and the development of osmoregulatory systems, including Na+/HCO3- cotransporter 1 (Nbce1), is crucial for their survival. This study investigated the expression of three isoforms of Nbce1 in the gills and intestine of salmon. The results suggest that tissue-specific modulation of Nbce1 isoforms contributes to the adaptive responses to seawater exposure in salmon.
The life history of Atlantic salmon (Salmo salar) includes an initial freshwater phase (parr) that precedes a springtime migration to marine environments as smolts. The development of osmoregulatory systems that will ultimately support the survival of juveniles upon entry into marine habitats is a key aspect of smoltification. While the acquisition of seawater tolerance in all euryhaline species demands the concerted activity of specific ion pumps, transporters, and channels, the contributions of Na+/HCO3- cotransporter 1 (Nbce1) to salinity acclimation remain unresolved. Here, we investigated the branchial and intestinal expression of three Na+/HCO3- cotransporter 1 isoforms, denoted nbce1.1, -1.2a, and -1.2b. Given the proposed role of Nbcel in supporting the absorption of environmental Na+ by ionocytes, we first hypothesized that expression of a branchial nbcel transcript (nbce1.2a) would be attenuated in salmon undergoing smoltification and following seawater exposure. In two separate years, we observed spring increases in branchial Na+/K+-ATPase activity, Na+/K+/2Cl(-) cotransporter 1, and cystic fibrosis transmembrane regulator 1 expression characteristic of smoltification, whereas there were no attendant changes in nbcel.2a expression. Nonetheless, branchial nbce1.2a levels were reduced in parr and smolts within 2 days of seawater exposure. In the intestine, gene transcript abundance for nbce1.1 increased from spring to summer in the anterior intestine, but not in the posterior intestine or pyloric caeca, and nbce1.1 and -1.2b expression in the intestine showed season-dependent transcriptional regulation by seawater exposure. Collectively, our data indicate that tissue-specific modulation of all three nbcel isoforms underlies adaptive responses to seawater.

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