Effect of Chum Salmon Egg Lectin on Tight Junctions in Caco-2 Cell Monolayers
The effect of a chum salmon egg lectin (CSL3) on tight junction (TJ) of Caco-2 cell monolayers was investigated. The lectin opened TJ as indicated by the decrease of the transepithelial electrical resistance (TER) value and the increase of the permeation of lucifer yellow, which is transported via t...
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doaj-e7fab53e505840c6820857cdde95f4952020-11-24T21:23:56ZengMDPI AGMolecules1420-30492015-05-012058094810610.3390/molecules20058094molecules20058094Effect of Chum Salmon Egg Lectin on Tight Junctions in Caco-2 Cell MonolayersRyo Nemoto0Shintaro Yamamoto1Tomohisa Ogawa2Ryno Naude3Koji Muramoto4Graduate School of Life Sciences, Tohoku University, Katahira 2-1-1, Aoba-ku, Sendai 980-8577, JapanGraduate School of Life Sciences, Tohoku University, Katahira 2-1-1, Aoba-ku, Sendai 980-8577, JapanGraduate School of Life Sciences, Tohoku University, Katahira 2-1-1, Aoba-ku, Sendai 980-8577, JapanDepartment of Biochemistry and Microbiology, Nelson Mandel Metropolitan University, Port Elizabeth 6031, South AfricaGraduate School of Life Sciences, Tohoku University, Katahira 2-1-1, Aoba-ku, Sendai 980-8577, JapanThe effect of a chum salmon egg lectin (CSL3) on tight junction (TJ) of Caco-2 cell monolayers was investigated. The lectin opened TJ as indicated by the decrease of the transepithelial electrical resistance (TER) value and the increase of the permeation of lucifer yellow, which is transported via the TJ-mediated paracellular pathway. The effects of CSL3 were inhibited by the addition of 10 mM L-rhamnose or D-galactose which were specific sugars for CSL3. The lectin increased the intracellular Ca2+ of Caco-2 cell monolayers, that could be inhibited by the addition of L-rhamnose. The fluorescence immunostaining of β-actin in Caco-2 cell monolayers revealed that the cytoskeleton was changed by the CSL3 treatment, suggesting that CSL3 depolymerized β-actin to cause reversible TJ structural and functional disruption. Although Japanese jack bean lectin and wheat germ lectin showed similar effects in the decrease of the TER values and the increase of the intracellular Ca2+, they could not be inhibited by the same concentrations of simple sugars, such as D-glucose and N-acetyl-D-glucosamine.http://www.mdpi.com/1420-3049/20/5/8094Caco-2 cellintestinal transportlectintight junctiontransepithelial transport |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Ryo Nemoto Shintaro Yamamoto Tomohisa Ogawa Ryno Naude Koji Muramoto |
spellingShingle |
Ryo Nemoto Shintaro Yamamoto Tomohisa Ogawa Ryno Naude Koji Muramoto Effect of Chum Salmon Egg Lectin on Tight Junctions in Caco-2 Cell Monolayers Molecules Caco-2 cell intestinal transport lectin tight junction transepithelial transport |
author_facet |
Ryo Nemoto Shintaro Yamamoto Tomohisa Ogawa Ryno Naude Koji Muramoto |
author_sort |
Ryo Nemoto |
title |
Effect of Chum Salmon Egg Lectin on Tight Junctions in Caco-2 Cell Monolayers |
title_short |
Effect of Chum Salmon Egg Lectin on Tight Junctions in Caco-2 Cell Monolayers |
title_full |
Effect of Chum Salmon Egg Lectin on Tight Junctions in Caco-2 Cell Monolayers |
title_fullStr |
Effect of Chum Salmon Egg Lectin on Tight Junctions in Caco-2 Cell Monolayers |
title_full_unstemmed |
Effect of Chum Salmon Egg Lectin on Tight Junctions in Caco-2 Cell Monolayers |
title_sort |
effect of chum salmon egg lectin on tight junctions in caco-2 cell monolayers |
publisher |
MDPI AG |
series |
Molecules |
issn |
1420-3049 |
publishDate |
2015-05-01 |
description |
The effect of a chum salmon egg lectin (CSL3) on tight junction (TJ) of Caco-2 cell monolayers was investigated. The lectin opened TJ as indicated by the decrease of the transepithelial electrical resistance (TER) value and the increase of the permeation of lucifer yellow, which is transported via the TJ-mediated paracellular pathway. The effects of CSL3 were inhibited by the addition of 10 mM L-rhamnose or D-galactose which were specific sugars for CSL3. The lectin increased the intracellular Ca2+ of Caco-2 cell monolayers, that could be inhibited by the addition of L-rhamnose. The fluorescence immunostaining of β-actin in Caco-2 cell monolayers revealed that the cytoskeleton was changed by the CSL3 treatment, suggesting that CSL3 depolymerized β-actin to cause reversible TJ structural and functional disruption. Although Japanese jack bean lectin and wheat germ lectin showed similar effects in the decrease of the TER values and the increase of the intracellular Ca2+, they could not be inhibited by the same concentrations of simple sugars, such as D-glucose and N-acetyl-D-glucosamine. |
topic |
Caco-2 cell intestinal transport lectin tight junction transepithelial transport |
url |
http://www.mdpi.com/1420-3049/20/5/8094 |
work_keys_str_mv |
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