Glutathione Transferases Responses Induced by Microcystin-LR in the Gills and Hepatopancreas of the Clam Venerupis philippinarum

A multi-method approach was employed to compare the responses of Glutatione Transferases (GSTs) in the gills and hepatopancreas of Venerupis philippinarum to microcystins (MCs) toxicity. In this way, using the cytosolic fraction, the enzymatic activity of GSTs, superoxide dismutase (SOD), serine/thr...

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Main Authors: Mariana Carneiro, Bruno Reis, Joana Azevedo, Alexandre Campos, Hugo Osório, Vítor Vasconcelos, José Carlos Martins
Format: Article
Language:English
Published: MDPI AG 2015-06-01
Series:Toxins
Subjects:
Online Access:http://www.mdpi.com/2072-6651/7/6/2096
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spelling doaj-be19b2431ca8472aa2fbd5febd3713662020-11-24T23:55:22ZengMDPI AGToxins2072-66512015-06-01762096212010.3390/toxins7062096toxins7062096Glutathione Transferases Responses Induced by Microcystin-LR in the Gills and Hepatopancreas of the Clam Venerupis philippinarumMariana Carneiro0Bruno Reis1Joana Azevedo2Alexandre Campos3Hugo Osório4Vítor Vasconcelos5José Carlos Martins6CIIMAR/CIMAR—Interdisciplinary Centre of Marine and Environmental Research, University of Porto, Rua dos Bragas 289, Porto 4050-123, PortugalCIIMAR/CIMAR—Interdisciplinary Centre of Marine and Environmental Research, University of Porto, Rua dos Bragas 289, Porto 4050-123, PortugalCIIMAR/CIMAR—Interdisciplinary Centre of Marine and Environmental Research, University of Porto, Rua dos Bragas 289, Porto 4050-123, PortugalCIIMAR/CIMAR—Interdisciplinary Centre of Marine and Environmental Research, University of Porto, Rua dos Bragas 289, Porto 4050-123, PortugalIPATIMUP—Institute of Molecular Pathology and Immunology of the University of Porto, Porto 4200-465, PortugalCIIMAR/CIMAR—Interdisciplinary Centre of Marine and Environmental Research, University of Porto, Rua dos Bragas 289, Porto 4050-123, PortugalCIIMAR/CIMAR—Interdisciplinary Centre of Marine and Environmental Research, University of Porto, Rua dos Bragas 289, Porto 4050-123, PortugalA multi-method approach was employed to compare the responses of Glutatione Transferases (GSTs) in the gills and hepatopancreas of Venerupis philippinarum to microcystins (MCs) toxicity. In this way, using the cytosolic fraction, the enzymatic activity of GSTs, superoxide dismutase (SOD), serine/threonine protein phosphatases (PPP2) along with the gene expression levels of four GST isoforms (pi, mu, sigma1, sigma2) were investigated in both organs of the clams exposed for 24 h to 10, 50 and 100 μg L−1 of MC-LR. Cytosolic GSTs (cGSTs) from both organs of the high dose exposed clams were purified by glutathione-agarose affinity chromatography, characterized kinetically and the changes in the expression of cGSTs of the gills identified using a proteomic approach. MC-LR caused an increase in GST enzyme activity, involved in conjugation reactions, in both gills and hepatopancreas (100 μg L−1 exposure). SOD activity, an indicator of oxidative stress, showed significantly elevated levels in the hepatopancreas only (50 and 100 μg L−1 exposure). No significant changes were found in PPP2 activity, the main target of MCs, for both organs. Transcription responses revealed an up-regulation of sigma2 in the hepatopancreas at the high dose, but no significant changes were detected in the gills. Kinetic analysis evidenced differences between gills of exposed and non-exposed extracts. Using proteomics, qualitative and quantitative differences were found between the basal and inducible cGSTs. Overall, results suggest a distinct role of GST system in counteracting MCs toxicity between the gills and the hepatopancreas of V. philippinarum, revealing different roles between GST isoforms within and among both organs.http://www.mdpi.com/2072-6651/7/6/2096microcystinsglutathione transferasesenzyme activityproteomicsreal-time PCRV. philippinarumdetoxificationbiomarker
collection DOAJ
language English
format Article
sources DOAJ
author Mariana Carneiro
Bruno Reis
Joana Azevedo
Alexandre Campos
Hugo Osório
Vítor Vasconcelos
José Carlos Martins
spellingShingle Mariana Carneiro
Bruno Reis
Joana Azevedo
Alexandre Campos
Hugo Osório
Vítor Vasconcelos
José Carlos Martins
Glutathione Transferases Responses Induced by Microcystin-LR in the Gills and Hepatopancreas of the Clam Venerupis philippinarum
Toxins
microcystins
glutathione transferases
enzyme activity
proteomics
real-time PCR
V. philippinarum
detoxification
biomarker
author_facet Mariana Carneiro
Bruno Reis
Joana Azevedo
Alexandre Campos
Hugo Osório
Vítor Vasconcelos
José Carlos Martins
author_sort Mariana Carneiro
title Glutathione Transferases Responses Induced by Microcystin-LR in the Gills and Hepatopancreas of the Clam Venerupis philippinarum
title_short Glutathione Transferases Responses Induced by Microcystin-LR in the Gills and Hepatopancreas of the Clam Venerupis philippinarum
title_full Glutathione Transferases Responses Induced by Microcystin-LR in the Gills and Hepatopancreas of the Clam Venerupis philippinarum
title_fullStr Glutathione Transferases Responses Induced by Microcystin-LR in the Gills and Hepatopancreas of the Clam Venerupis philippinarum
title_full_unstemmed Glutathione Transferases Responses Induced by Microcystin-LR in the Gills and Hepatopancreas of the Clam Venerupis philippinarum
title_sort glutathione transferases responses induced by microcystin-lr in the gills and hepatopancreas of the clam venerupis philippinarum
publisher MDPI AG
series Toxins
issn 2072-6651
publishDate 2015-06-01
description A multi-method approach was employed to compare the responses of Glutatione Transferases (GSTs) in the gills and hepatopancreas of Venerupis philippinarum to microcystins (MCs) toxicity. In this way, using the cytosolic fraction, the enzymatic activity of GSTs, superoxide dismutase (SOD), serine/threonine protein phosphatases (PPP2) along with the gene expression levels of four GST isoforms (pi, mu, sigma1, sigma2) were investigated in both organs of the clams exposed for 24 h to 10, 50 and 100 μg L−1 of MC-LR. Cytosolic GSTs (cGSTs) from both organs of the high dose exposed clams were purified by glutathione-agarose affinity chromatography, characterized kinetically and the changes in the expression of cGSTs of the gills identified using a proteomic approach. MC-LR caused an increase in GST enzyme activity, involved in conjugation reactions, in both gills and hepatopancreas (100 μg L−1 exposure). SOD activity, an indicator of oxidative stress, showed significantly elevated levels in the hepatopancreas only (50 and 100 μg L−1 exposure). No significant changes were found in PPP2 activity, the main target of MCs, for both organs. Transcription responses revealed an up-regulation of sigma2 in the hepatopancreas at the high dose, but no significant changes were detected in the gills. Kinetic analysis evidenced differences between gills of exposed and non-exposed extracts. Using proteomics, qualitative and quantitative differences were found between the basal and inducible cGSTs. Overall, results suggest a distinct role of GST system in counteracting MCs toxicity between the gills and the hepatopancreas of V. philippinarum, revealing different roles between GST isoforms within and among both organs.
topic microcystins
glutathione transferases
enzyme activity
proteomics
real-time PCR
V. philippinarum
detoxification
biomarker
url http://www.mdpi.com/2072-6651/7/6/2096
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