<p>Rainbow trout epithelial cell lines from the gill, RTgill-W1, and gut, RTgutGC, were exposed to NH<sub>4</sub>Cl at 18–21&#xa0;°C in L15 (basal medium) with fetal bovine serum and were found to undergo cytoplasmic vacuolization and cell death, depending on NH<sub>4</sub>Cl concentration and exposure time. Vacuolization arose within 24&#xa0;h of cultures being exposed to 10–100&#xa0;mM NH<sub>4</sub>Cl, and vacuoles disappeared over 24&#xa0;h after NH<sub>4</sub>Cl-exposed cultures were returned to just L15/FBS. RTgill-W1 appeared more sensitive to vacuolization, with one indicator being the maximal proportion of vacuolated cells in a culture, which approached 100% in 50&#xa0;mM NH<sub>4</sub>Cl for 72&#xa0;h. RTgill-W1 also were more sensitive to NH<sub>4</sub>Cl-induced cell killing. For 7-d exposures, the inhibitory concentrations (IC50s) for the 50% loss of cell viability as evaluated with Alamar Blue were 30&#xa0;mM NH<sub>4</sub>Cl for RTgill-W1 and 80&#xa0;mM for RTgutGC. In a wound-healing assay, RTgutGC cells in 0.1 and 1&#xa0;mM NH<sub>4</sub>Cl were able to migrate and cover a 500-μm gap in 5 d, like the control, but in 50&#xa0;mM NH<sub>4</sub>Cl healing was blocked. In 10&#xa0;mM NH<sub>4</sub>Cl, repair was slowed but by 14 d the gap was covered with cells and many of these were vacuolated. Overall, the results provide a foundation for using these two cell lines to study the physiology and toxicology of ammonia in fish.</p>

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Response of epithelial cell lines from the rainbow trout gut and gill to ammonia

  • Daylan T. Pritchard,
  • Caio J. Nicholson de Figueiroa,
  • Niels C. Bols,
  • Lucy E. J. Lee

摘要

Rainbow trout epithelial cell lines from the gill, RTgill-W1, and gut, RTgutGC, were exposed to NH4Cl at 18–21 °C in L15 (basal medium) with fetal bovine serum and were found to undergo cytoplasmic vacuolization and cell death, depending on NH4Cl concentration and exposure time. Vacuolization arose within 24 h of cultures being exposed to 10–100 mM NH4Cl, and vacuoles disappeared over 24 h after NH4Cl-exposed cultures were returned to just L15/FBS. RTgill-W1 appeared more sensitive to vacuolization, with one indicator being the maximal proportion of vacuolated cells in a culture, which approached 100% in 50 mM NH4Cl for 72 h. RTgill-W1 also were more sensitive to NH4Cl-induced cell killing. For 7-d exposures, the inhibitory concentrations (IC50s) for the 50% loss of cell viability as evaluated with Alamar Blue were 30 mM NH4Cl for RTgill-W1 and 80 mM for RTgutGC. In a wound-healing assay, RTgutGC cells in 0.1 and 1 mM NH4Cl were able to migrate and cover a 500-μm gap in 5 d, like the control, but in 50 mM NH4Cl healing was blocked. In 10 mM NH4Cl, repair was slowed but by 14 d the gap was covered with cells and many of these were vacuolated. Overall, the results provide a foundation for using these two cell lines to study the physiology and toxicology of ammonia in fish.