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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Main Authors: Ryo Nemoto, Shintaro Yamamoto, Tomohisa Ogawa, Ryno Naude, Koji Muramoto
Format: Article
Language:English
Published: MDPI AG 2015-05-01
Series:Molecules
Subjects:
Online Access:http://www.mdpi.com/1420-3049/20/5/8094
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spelling 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
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