Abstract

BackgroundTeleosts 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.ResultsUsing 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.ConclusionsThe 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.

Highlights

  • 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

  • Studies on osmoregulation have focused on the transport of ions to drive water movement and it is generally accepted that ions in the extracellular fluid (ECF) are regulated at a relatively constant level to maintain plasma osmolality in most vertebrates

  • Partial purification of Na-binding molecules from esophageal and intestinal secretion using size exclusion chromatography Since we discovered the Na-binding molecules could be rich in the mucus of esophagus and intestine from histology and electron probe micro-analyzer (EPMA) data, we attempted to partially purify the molecules using gel filtration chromatography, exploiting Na-binding characteristics of the molecules in the detection system

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Summary

Introduction

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. Wong et al Zoological Letters (2017) 3:22 diluted urine in FW [7, 8] while those in SW actively secrete divalent ions in the proximal tubules [9,10,11]. These mechanisms were mostly derived from studies using euryhaline species (e.g. eels, salmon, killifish, etc.) fully acclimated to either FW or SW, whereas knowledge during the early transition phase between salinities is limited. Japanese medaka is a moderate euryhaline species and FW medaka can acclimate to 2/3 SW directly with a significant increase in plasma Na+ within 3 h after the transfer (Table 1)

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