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A sodium binding system alleviates acute salt stress during seawater acclimation in eels
BACKGROUND: Teleosts transiting from freshwater (FW) to seawater (SW) environments face an immediate osmotic stress from ion influxes and water loss, but some euryhaline species such as eels can maintain a stable plasma osmolality during early SW exposure. The time course changes in the gene express...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5727781/ https://www.ncbi.nlm.nih.gov/pubmed/29255617 http://dx.doi.org/10.1186/s40851-017-0081-8 |
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author | Wong, Marty Kwok Shing Tsukada, Takehiro Ogawa, Nobuhiro Pipil, Supriya Ozaki, Haruka Suzuki, Yutaka Iwasaki, Wataru Takei, Yoshio |
author_facet | Wong, Marty Kwok Shing Tsukada, Takehiro Ogawa, Nobuhiro Pipil, Supriya Ozaki, Haruka Suzuki, Yutaka Iwasaki, Wataru Takei, Yoshio |
author_sort | Wong, Marty Kwok Shing |
collection | PubMed |
description | BACKGROUND: Teleosts transiting from freshwater (FW) to seawater (SW) environments face an immediate osmotic stress from ion influxes and water loss, but some euryhaline species such as eels can maintain a stable plasma osmolality during early SW exposure. The time course changes in the gene expression, protein abundance, and localization of key ion transporters suggested that the reversal of the ion transport systems was gradual, and we investigate how eels utilize a Na-binding strategy to slow down the ion invasion and complement the transporter-mediated osmoregulation. RESULTS: Using an electron probe micro-analyzer, we localized bound Na in various eel tissues in response to SW transfer, suggesting that the Na-binding molecules were produced to sequester excess ionic Na(+) to negate its osmotic potential, thus preventing acute cellular dehydration. Mucus cells were acutely activated in digestive tract, gill, and skin after SW transfer, producing Na-binding molecule-containing mucus layers that fence off high osmolality of SW. Using gel filtration HPLC, some molecules at 18 kDa were found to bind Na in the luminal secretion of esophagus and intestine, and higher binding was associated with SW transfer. Transcriptome and protein interaction results indicated that downregulation of Notch and β-catenin pathways, and dynamic changes in TGFβ pathways in intestine were involved during early SW transition, supporting the observed histological changes on epithelial desquamation and increased mucus production. CONCLUSIONS: The timing for the activation of the Na-binding mechanism to alleviate the adverse osmotic gradient was temporally complementary to the subsequent remodeling of branchial ionocytes and transporting epithelia of the digestive tract. The strategy to manipulate the osmotic potential of Na(+) by specific binding molecules is similar to the osmotically inactive Na described in human skin and muscle. The Na-binding molecules provide a buffer to tolerate the salinity changes, which is advantageous to the estuary and migrating fishes. Our data pave the way to identify this unknown class of molecules and open a new area of vertebrate osmoregulation research. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s40851-017-0081-8) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5727781 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-57277812017-12-18 A sodium binding system alleviates acute salt stress during seawater acclimation in eels Wong, Marty Kwok Shing Tsukada, Takehiro Ogawa, Nobuhiro Pipil, Supriya Ozaki, Haruka Suzuki, Yutaka Iwasaki, Wataru Takei, Yoshio Zoological Lett Research Article BACKGROUND: Teleosts transiting from freshwater (FW) to seawater (SW) environments face an immediate osmotic stress from ion influxes and water loss, but some euryhaline species such as eels can maintain a stable plasma osmolality during early SW exposure. The time course changes in the gene expression, protein abundance, and localization of key ion transporters suggested that the reversal of the ion transport systems was gradual, and we investigate how eels utilize a Na-binding strategy to slow down the ion invasion and complement the transporter-mediated osmoregulation. RESULTS: Using an electron probe micro-analyzer, we localized bound Na in various eel tissues in response to SW transfer, suggesting that the Na-binding molecules were produced to sequester excess ionic Na(+) to negate its osmotic potential, thus preventing acute cellular dehydration. Mucus cells were acutely activated in digestive tract, gill, and skin after SW transfer, producing Na-binding molecule-containing mucus layers that fence off high osmolality of SW. Using gel filtration HPLC, some molecules at 18 kDa were found to bind Na in the luminal secretion of esophagus and intestine, and higher binding was associated with SW transfer. Transcriptome and protein interaction results indicated that downregulation of Notch and β-catenin pathways, and dynamic changes in TGFβ pathways in intestine were involved during early SW transition, supporting the observed histological changes on epithelial desquamation and increased mucus production. CONCLUSIONS: The timing for the activation of the Na-binding mechanism to alleviate the adverse osmotic gradient was temporally complementary to the subsequent remodeling of branchial ionocytes and transporting epithelia of the digestive tract. The strategy to manipulate the osmotic potential of Na(+) by specific binding molecules is similar to the osmotically inactive Na described in human skin and muscle. The Na-binding molecules provide a buffer to tolerate the salinity changes, which is advantageous to the estuary and migrating fishes. Our data pave the way to identify this unknown class of molecules and open a new area of vertebrate osmoregulation research. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s40851-017-0081-8) contains supplementary material, which is available to authorized users. BioMed Central 2017-12-12 /pmc/articles/PMC5727781/ /pubmed/29255617 http://dx.doi.org/10.1186/s40851-017-0081-8 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Wong, Marty Kwok Shing Tsukada, Takehiro Ogawa, Nobuhiro Pipil, Supriya Ozaki, Haruka Suzuki, Yutaka Iwasaki, Wataru Takei, Yoshio A sodium binding system alleviates acute salt stress during seawater acclimation in eels |
title | A sodium binding system alleviates acute salt stress during seawater acclimation in eels |
title_full | A sodium binding system alleviates acute salt stress during seawater acclimation in eels |
title_fullStr | A sodium binding system alleviates acute salt stress during seawater acclimation in eels |
title_full_unstemmed | A sodium binding system alleviates acute salt stress during seawater acclimation in eels |
title_short | A sodium binding system alleviates acute salt stress during seawater acclimation in eels |
title_sort | sodium binding system alleviates acute salt stress during seawater acclimation in eels |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5727781/ https://www.ncbi.nlm.nih.gov/pubmed/29255617 http://dx.doi.org/10.1186/s40851-017-0081-8 |
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