Hexavalent chromium is cytotoxic and genotoxic to hawksbill sea turtle cells
Creators
- 1. Department of Applied Medical Science, University of Southern Maine, Science Building, 96 Falmouth Street, Portland, ME 04103 (United States)
- 2. Maine Center for Toxicology and Environmental Health, University of Southern Maine, Science Building, 96 Falmouth Street, Portland, ME 04103 (United States)
- 3. Wise Laboratory of Environmental and Genetic Toxicology, University of Southern Maine, Science Building, 96 Falmouth Street, Portland, ME 04103 (United States)
- 4. Graduate School of Agricultural Sciences, Tohoku University, Laboratory of Animal Breeding and Genetics, Second Research Building, Rm 112, 1-1 Amamiyamachi, Aoba-ku, Sendai 981-8555 (Japan)
Description
Sea turtles are a charismatic and ancient ocean species and can serve as key indicators for ocean ecosystems, including coral reefs and sea grass beds as well as coastal beaches. Genotoxicity studies in the species are absent, limiting our understanding of the impact of environmental toxicants on sea turtles. Hexavalent chromium (Cr(VI)) is a ubiquitous environmental problem worldwide, and recent studies show it is a global marine pollutant of concern. Thus, we evaluated the cytotoxicity and genotoxicity of soluble and particulate Cr(VI) in hawksbill sea turtle cells. Particulate Cr(VI) was both cytotoxic and genotoxic to sea turtle cells. Concentrations of 0.1, 0.5, 1, and 5 μg/cm2 lead chromate induced 108, 79, 54, and 7% relative survival, respectively. Additionally, concentrations of 0, 0.1, 0.5, 1, and 5 μg/cm2 lead chromate induced damage in 4, 10, 15, 26, and 36% of cells and caused 4, 11, 17, 30, and 56 chromosome aberrations in 100 metaphases, respectively. For soluble Cr, concentrations of 0.25, 0.5, 1, 2.5, and 5 μM sodium chromate induced 84, 69, 46, 25, and 3% relative survival, respectively. Sodium chromate induced 3, 9, 9, 14, 21, and 29% of metaphases with damage, and caused 3, 10, 10, 16, 26, and 39 damaged chromosomes in 100 metaphases at concentrations of 0, 0.25, 0.5, 1, 2.5, and 5 μM sodium chromate, respectively. These data suggest that Cr(VI) may be a concern for hawksbill sea turtles and sea turtles in general. - Highlights: • Particulate Cr(VI) is cytotoxic and clastogenic to hawksbill sea turtle cells. • Soluble Cr(VI) is cytotoxic and clastogenic to hawksbill sea turtle cells. • Cr(VI) may be a risk factor for hawksbill sea turtle health
Availability note (English)
Available from http://dx.doi.org/10.1016/j.taap.2014.06.008Additional details
Identifiers
- DOI
- 10.1016/j.taap.2014.06.008;
- PII
- S0041-008X(14)00231-2;
Publishing Information
- Journal Title
- Toxicology and Applied Pharmacology
- Journal Volume
- 279
- Journal Issue
- 2
- Journal Page Range
- p. 113-118
- ISSN
- 0041-008X
- CODEN
- TXAPA9
INIS
- Country of Publication
- United States
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 47009344
- Subject category
- S60: APPLIED LIFE SCIENCES;
- Descriptors DEI
- CHROMIUM; CHROMOSOMAL ABERRATIONS; CHROMOSOMES; COASTAL REGIONS; CONCENTRATION RATIO; CORAL REEFS; ECOSYSTEMS; GRAMINEAE; HAZARDS; LEAD; MITOSIS; POLLUTANTS; SEAS; SODIUM; TOXICITY; TURTLES
- Descriptors DEC
- ALKALI METALS; ANIMALS; CELL DIVISION; DIMENSIONLESS NUMBERS; ELEMENTS; GEOLOGIC STRUCTURES; LILIOPSIDA; MAGNOLIOPHYTA; METALS; MUTATIONS; PLANTS; REEFS; REPTILES; SURFACE WATERS; TRANSITION ELEMENTS; VERTEBRATES
Optional Information
- Copyright
- Copyright (c) 2014 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.