Abstract |
The potent neurotoxin saxitoxin produced by both marine and freshwater phytoplankton causes paralytic shellfish poisoning syndrome. The toxicity and mode of action of the acute exposure of high-dose saxitoxin have been intensively studied for decades; however, the potential risk of exposure of low-dose saxitoxin remained to be uncovered. Here we present a proteomics study of murine neuroblastoma N2A cell with low-dose saxitoxin exposure (1 nM and 10 nM, 24-h intoxication). Differential proteins were profiled by two-dimensional fluorescence difference gel electrophoresis (2D-DIGE) coupled with matrix-assisted laser desorption/ionization time of flight mass spectrometry (MALDI-TOF-MS). A total of 9 proteins, including 14-3-3 beta (1433B), alpha enolase (ENO1) and cofilin 2 (CFL2), were altered by the low-dose saxitoxin exposure. We further validated the expressions of 1433B, ENO1 and CFL2 by Western blot analysis and the enzyme-linked immunosorbent assay. These 9 proteins involve cell apoptotic pathways, cell skeleton maintenance, membrane potentials and mitochondrial functions. Modulation of these 9 proteins by low-dose saxitoxin exposure could correlate to the reports on genotoxicity and neurotoxicity induced by saxitoxin. This study also suggested other potential risks of saxitoxin.
|
Authors | Xiao Chen, Ye Sun, Haiyan Huang, Wei Liu, Panpan Hu, Xinfeng Huang, Fei Zou, Jianjun Liu |
Journal | Toxicology mechanisms and methods
(Toxicol Mech Methods)
Vol. 28
Issue 5
Pg. 335-344
(Jun 2018)
ISSN: 1537-6524 [Electronic] England |
PMID | 29228856
(Publication Type: Journal Article)
|
Chemical References |
- 14-3-3 Proteins
- Cfl2 protein, mouse
- Cofilin 2
- Proteome
- Saxitoxin
- Eno1 protein, mouse
- Phosphopyruvate Hydratase
|
Topics |
- 14-3-3 Proteins
(metabolism)
- Animals
- Blotting, Western
- Cell Line, Tumor
- Cofilin 2
(metabolism)
- Dose-Response Relationship, Drug
- Enzyme-Linked Immunosorbent Assay
- Mice
- Neuroblastoma
(metabolism, pathology)
- Neurons
(drug effects, metabolism, pathology)
- Phosphopyruvate Hydratase
(metabolism)
- Proteome
(drug effects, metabolism)
- Proteomics
(methods)
- Risk Assessment
- Saxitoxin
(toxicity)
- Signal Transduction
(drug effects)
- Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization
- Toxicity Tests
(methods)
- Two-Dimensional Difference Gel Electrophoresis
|