ACUTE NITRATE EXPOSURE CAUSES PROTEOMIC CHANGES CONSISTENT WITH THE REGULATION OF REACTIVE OXYGEN AND NITROGEN SPECIES

Nitrate is the most common ionic form of nitrogen in aquatic ecosystems. Although nitrate is known to affect ecosystems at high levels through eutrophication, hypoxia and loss of biodiversity, it is considered to be physiologically inert to the individual aquatic organism. To test the physiologica...

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Main Authors: Hitt, Lauren R, Tomanek, Lars
Format: Others
Published: DigitalCommons@CalPoly 2009
Subjects:
Online Access:https://digitalcommons.calpoly.edu/theses/95
https://digitalcommons.calpoly.edu/cgi/viewcontent.cgi?article=1106&context=theses
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spelling ndltd-CALPOLY-oai-digitalcommons.calpoly.edu-theses-11062019-10-24T15:12:48Z ACUTE NITRATE EXPOSURE CAUSES PROTEOMIC CHANGES CONSISTENT WITH THE REGULATION OF REACTIVE OXYGEN AND NITROGEN SPECIES Hitt, Lauren R Tomanek, Lars Nitrate is the most common ionic form of nitrogen in aquatic ecosystems. Although nitrate is known to affect ecosystems at high levels through eutrophication, hypoxia and loss of biodiversity, it is considered to be physiologically inert to the individual aquatic organism. To test the physiological effects of nitrate on aquatic life, we exposed gill tissue of the Pacific oyster, Crassostrea gigas, to nitrate and characterized changes in protein expression, using a gel-based proteomics approach. Of the 642 protein spots detected, we found that 24 proteins (15 identified) changed expression in response to a 6-hour exposure to nitrate concentrations ranging from 0-73 mg/L, values that characterize highly contaminated surface and ground waters. Proteins changing expression included the oxidative stress proteins thioredoxin and cavortin (a member of the superoxide dismutase family) as well as proteins that are involved in G-protein signaling (Rho-GDI, ADP-ribosylation factor, G-protein ß-subunit), protein homeostasis (heat shock protein 70, prohibitin, calreticulin, and proteasome &#;-type 4 subunit), glycolysis (enolase), transport of hydrophobic molecules (lipocalin) and cytoskeletal arrangements (intermediate filaments and a gelsolin-like adseverin). The most parsimonious explanation for these changes in protein expression assumes that C. gigas reduces nitrate to nitrite and nitric oxide, which reacts with superoxide anions to form the very reactive peroxynitrite. We propose that part of the cellular response to reactive nitrogen species,phagocytic hemocytes inhibit the production of reactive oxygen species, potentially compromising the immune response of oysters to invading pathogens. 2009-06-01T07:00:00Z text application/pdf https://digitalcommons.calpoly.edu/theses/95 https://digitalcommons.calpoly.edu/cgi/viewcontent.cgi?article=1106&context=theses Master's Theses and Project Reports DigitalCommons@CalPoly environmental proteomics Systems and Integrative Physiology
collection NDLTD
format Others
sources NDLTD
topic environmental proteomics
Systems and Integrative Physiology
spellingShingle environmental proteomics
Systems and Integrative Physiology
Hitt, Lauren R
Tomanek, Lars
ACUTE NITRATE EXPOSURE CAUSES PROTEOMIC CHANGES CONSISTENT WITH THE REGULATION OF REACTIVE OXYGEN AND NITROGEN SPECIES
description Nitrate is the most common ionic form of nitrogen in aquatic ecosystems. Although nitrate is known to affect ecosystems at high levels through eutrophication, hypoxia and loss of biodiversity, it is considered to be physiologically inert to the individual aquatic organism. To test the physiological effects of nitrate on aquatic life, we exposed gill tissue of the Pacific oyster, Crassostrea gigas, to nitrate and characterized changes in protein expression, using a gel-based proteomics approach. Of the 642 protein spots detected, we found that 24 proteins (15 identified) changed expression in response to a 6-hour exposure to nitrate concentrations ranging from 0-73 mg/L, values that characterize highly contaminated surface and ground waters. Proteins changing expression included the oxidative stress proteins thioredoxin and cavortin (a member of the superoxide dismutase family) as well as proteins that are involved in G-protein signaling (Rho-GDI, ADP-ribosylation factor, G-protein ß-subunit), protein homeostasis (heat shock protein 70, prohibitin, calreticulin, and proteasome &#;-type 4 subunit), glycolysis (enolase), transport of hydrophobic molecules (lipocalin) and cytoskeletal arrangements (intermediate filaments and a gelsolin-like adseverin). The most parsimonious explanation for these changes in protein expression assumes that C. gigas reduces nitrate to nitrite and nitric oxide, which reacts with superoxide anions to form the very reactive peroxynitrite. We propose that part of the cellular response to reactive nitrogen species,phagocytic hemocytes inhibit the production of reactive oxygen species, potentially compromising the immune response of oysters to invading pathogens.
author Hitt, Lauren R
Tomanek, Lars
author_facet Hitt, Lauren R
Tomanek, Lars
author_sort Hitt, Lauren R
title ACUTE NITRATE EXPOSURE CAUSES PROTEOMIC CHANGES CONSISTENT WITH THE REGULATION OF REACTIVE OXYGEN AND NITROGEN SPECIES
title_short ACUTE NITRATE EXPOSURE CAUSES PROTEOMIC CHANGES CONSISTENT WITH THE REGULATION OF REACTIVE OXYGEN AND NITROGEN SPECIES
title_full ACUTE NITRATE EXPOSURE CAUSES PROTEOMIC CHANGES CONSISTENT WITH THE REGULATION OF REACTIVE OXYGEN AND NITROGEN SPECIES
title_fullStr ACUTE NITRATE EXPOSURE CAUSES PROTEOMIC CHANGES CONSISTENT WITH THE REGULATION OF REACTIVE OXYGEN AND NITROGEN SPECIES
title_full_unstemmed ACUTE NITRATE EXPOSURE CAUSES PROTEOMIC CHANGES CONSISTENT WITH THE REGULATION OF REACTIVE OXYGEN AND NITROGEN SPECIES
title_sort acute nitrate exposure causes proteomic changes consistent with the regulation of reactive oxygen and nitrogen species
publisher DigitalCommons@CalPoly
publishDate 2009
url https://digitalcommons.calpoly.edu/theses/95
https://digitalcommons.calpoly.edu/cgi/viewcontent.cgi?article=1106&context=theses
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