4.5 Article

Proteomic response to elevated PCO2 level in eastern oysters, Crassostrea virginica: evidence for oxidative stress

期刊

JOURNAL OF EXPERIMENTAL BIOLOGY
卷 214, 期 11, 页码 1836-1844

出版社

COMPANY BIOLOGISTS LTD
DOI: 10.1242/jeb.055475

关键词

cytoskeleton; estuary; hypercapnia; proteomics; oxidative stress; oyster

类别

资金

  1. National Science Foundation [IOS-0717087, IOS-0951079]
  2. North Carolina Sea Grant Minigrant [R/MG-0906]
  3. UNC Charlotte Faculty
  4. Direct For Biological Sciences
  5. Emerging Frontiers [1041227] Funding Source: National Science Foundation
  6. Division Of Integrative Organismal Systems
  7. Direct For Biological Sciences [0951139] Funding Source: National Science Foundation

向作者/读者索取更多资源

Estuaries are characterized by extreme fluctuations in CO2 levels due to bouts of CO2 production by the resident biota that exceed its capacity of CO2 consumption and/or the rates of gas exchange with the atmosphere and open ocean waters. Elevated partial pressures of CO2 (P-CO2; i.e. environmental hypercapnia) decrease the pH of estuarine waters and, ultimately, extracellular and intracellular pH levels of estuarine organisms such as mollusks that have limited capacity for pH regulation. We analyzed proteomic changes associated with exposure to elevated P-CO2 in the mantle tissue of eastern oysters (Crassostrea virginica) after 2. weeks of exposure to control (similar to 39 Pa P-CO2) and hypercapnic (similar to 357 Pa P-CO2) conditions using two-dimensional gel electrophoresis and tandem mass spectrometry. Exposure to high P-CO2 resulted in a significant proteome shift in the mantle tissue, with 12% of proteins (54 out of 456) differentially expressed under the high P-CO2 compared with control conditions. Of the 54 differentially expressed proteins, we were able to identify 17. Among the identified proteins, two main functional categories were upregulated in response to hypercapnia: those associated with the cytoskeleton (e. g. several actin isoforms) and those associated with oxidative stress (e.g. superoxide dismutase and several peroxiredoxins as well as the thioredoxin-related nucleoredoxin). This indicates that exposure to high P-CO2 (similar to 357 Pa) induces oxidative stress and suggests that the cytoskeleton is a major target of oxidative stress. We discuss how elevated CO2 levels may cause oxidative stress by increasing the production of reactive oxygen species (ROS) either indirectly by lowering organismal pH, which may enhance the Fenton reaction, and/or directly by CO2 interacting with other ROS to form more free radicals. Although estuarine species are already exposed to higher and more variable levels of CO2 than other marine species, climate change may further increase the extremes and thereby cause greater levels of oxidative stress.

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