Cellular and Transcriptional Responses of Crassostrea gigas Hemocytes Exposed in Vitro to Brevetoxin (PbTx-2)

Hemocytes mediate a series of immune reactions essential for bivalve survival in the environment, however, the impact of harmful algal species and their associated phycotoxins upon bivalve immune system is under debate. To better understand the possible toxic effects of these toxins, Crassostrea gig...

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Published in:Marine Drugs
Main Authors: Danielle F. Mello, Eliza S. De Oliveira, Renato C. Vieira, Erik Simoes, Rafael Trevisan, Alcir Luiz Dafre, Margherita Anna Barracco
Format: Text
Language:English
Published: Molecular Diversity Preservation International 2012
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Online Access:https://doi.org/10.3390/md10030583
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spelling ftmdpi:oai:mdpi.com:/1660-3397/10/3/583/ 2023-08-20T04:06:01+02:00 Cellular and Transcriptional Responses of Crassostrea gigas Hemocytes Exposed in Vitro to Brevetoxin (PbTx-2) Danielle F. Mello Eliza S. De Oliveira Renato C. Vieira Erik Simoes Rafael Trevisan Alcir Luiz Dafre Margherita Anna Barracco agris 2012-03-05 application/pdf https://doi.org/10.3390/md10030583 EN eng Molecular Diversity Preservation International https://dx.doi.org/10.3390/md10030583 https://creativecommons.org/licenses/by/3.0/ Marine Drugs; Volume 10; Issue 3; Pages: 583-597 brevetoxin hemocytes bivalves gene expression immune antioxidant and detoxification systems Text 2012 ftmdpi https://doi.org/10.3390/md10030583 2023-07-31T20:28:22Z Hemocytes mediate a series of immune reactions essential for bivalve survival in the environment, however, the impact of harmful algal species and their associated phycotoxins upon bivalve immune system is under debate. To better understand the possible toxic effects of these toxins, Crassostrea gigas hemocytes were exposed to brevetoxin (PbTx-2). Hemocyte viability, monitored through the neutral red retention and MTT reduction assays, and apoptosis (Hoechst staining) remained unchanged during 12 h of exposure to PbTx-2 in concentrations up to 1000 µg/L. Despite cell viability and apoptosis remained stable, hemocytes incubated for 4 h with 1000 µg/L of PbTx-2 revealed higher expression levels of Hsp70 (p < 0.01) and CYP356A1 ( p < 0.05) transcripts and a tendency to increase FABP expression, as evaluated by Real-Time quantitative PCR. The expression of other studied genes (BPI, IL-17, GSTO, EcSOD, Prx6, SOD and GPx) remained unchanged. The results suggest that the absence of cytotoxic effects of PbTx-2 in Crassostrea gigas hemocytes, even at high concentrations, allow early defense responses to be produced by activating protective mechanisms associated to detoxification (CYP356A1 and possibly FABP) and stress (Hsp70), but not to immune or to antioxidant (BPI, IL-17, EcSOD, Prx6, GPx and SOD) related genes. Text Crassostrea gigas MDPI Open Access Publishing Marine Drugs 10 12 583 597
institution Open Polar
collection MDPI Open Access Publishing
op_collection_id ftmdpi
language English
topic brevetoxin
hemocytes
bivalves
gene expression
immune
antioxidant and detoxification systems
spellingShingle brevetoxin
hemocytes
bivalves
gene expression
immune
antioxidant and detoxification systems
Danielle F. Mello
Eliza S. De Oliveira
Renato C. Vieira
Erik Simoes
Rafael Trevisan
Alcir Luiz Dafre
Margherita Anna Barracco
Cellular and Transcriptional Responses of Crassostrea gigas Hemocytes Exposed in Vitro to Brevetoxin (PbTx-2)
topic_facet brevetoxin
hemocytes
bivalves
gene expression
immune
antioxidant and detoxification systems
description Hemocytes mediate a series of immune reactions essential for bivalve survival in the environment, however, the impact of harmful algal species and their associated phycotoxins upon bivalve immune system is under debate. To better understand the possible toxic effects of these toxins, Crassostrea gigas hemocytes were exposed to brevetoxin (PbTx-2). Hemocyte viability, monitored through the neutral red retention and MTT reduction assays, and apoptosis (Hoechst staining) remained unchanged during 12 h of exposure to PbTx-2 in concentrations up to 1000 µg/L. Despite cell viability and apoptosis remained stable, hemocytes incubated for 4 h with 1000 µg/L of PbTx-2 revealed higher expression levels of Hsp70 (p < 0.01) and CYP356A1 ( p < 0.05) transcripts and a tendency to increase FABP expression, as evaluated by Real-Time quantitative PCR. The expression of other studied genes (BPI, IL-17, GSTO, EcSOD, Prx6, SOD and GPx) remained unchanged. The results suggest that the absence of cytotoxic effects of PbTx-2 in Crassostrea gigas hemocytes, even at high concentrations, allow early defense responses to be produced by activating protective mechanisms associated to detoxification (CYP356A1 and possibly FABP) and stress (Hsp70), but not to immune or to antioxidant (BPI, IL-17, EcSOD, Prx6, GPx and SOD) related genes.
format Text
author Danielle F. Mello
Eliza S. De Oliveira
Renato C. Vieira
Erik Simoes
Rafael Trevisan
Alcir Luiz Dafre
Margherita Anna Barracco
author_facet Danielle F. Mello
Eliza S. De Oliveira
Renato C. Vieira
Erik Simoes
Rafael Trevisan
Alcir Luiz Dafre
Margherita Anna Barracco
author_sort Danielle F. Mello
title Cellular and Transcriptional Responses of Crassostrea gigas Hemocytes Exposed in Vitro to Brevetoxin (PbTx-2)
title_short Cellular and Transcriptional Responses of Crassostrea gigas Hemocytes Exposed in Vitro to Brevetoxin (PbTx-2)
title_full Cellular and Transcriptional Responses of Crassostrea gigas Hemocytes Exposed in Vitro to Brevetoxin (PbTx-2)
title_fullStr Cellular and Transcriptional Responses of Crassostrea gigas Hemocytes Exposed in Vitro to Brevetoxin (PbTx-2)
title_full_unstemmed Cellular and Transcriptional Responses of Crassostrea gigas Hemocytes Exposed in Vitro to Brevetoxin (PbTx-2)
title_sort cellular and transcriptional responses of crassostrea gigas hemocytes exposed in vitro to brevetoxin (pbtx-2)
publisher Molecular Diversity Preservation International
publishDate 2012
url https://doi.org/10.3390/md10030583
op_coverage agris
genre Crassostrea gigas
genre_facet Crassostrea gigas
op_source Marine Drugs; Volume 10; Issue 3; Pages: 583-597
op_relation https://dx.doi.org/10.3390/md10030583
op_rights https://creativecommons.org/licenses/by/3.0/
op_doi https://doi.org/10.3390/md10030583
container_title Marine Drugs
container_volume 10
container_issue 12
container_start_page 583
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