header logo image header logo text
Downloads Login
Research
General Information
ZIRC
ZFIN ID: ZDB-PUB-110214-12
Abnormal development of motor neurons in perfluorooctane sulphonate exposed zebrafish embryos
Zhang, L., Li, Y.Y., Chen, T., Xia, W., Zhou, Y., Wan, Y.J., Lv, Z.Q., Li, G.Q., and Xu, S.Q.
Date: 2011
Source: Ecotoxicology (London, England)   20(4): 643-52 (Journal)
Registered Authors:
Keywords: Motor neurons, Oxidative stress, PFOS, Neurodevelopmental toxicity, Zebrafish
MeSH Terms:
  • Alkanesulfonic Acids/toxicity*
  • Animals
  • Cell Proliferation/drug effects
  • Cyclin-Dependent Kinase 5/genetics
  • Cyclin-Dependent Kinase 5/metabolism
  • Dose-Response Relationship, Drug
  • Embryo, Nonmammalian/abnormalities
  • Embryo, Nonmammalian/drug effects*
  • Fluorocarbons/toxicity*
  • Gene Expression/drug effects
  • Growth and Development/drug effects
  • Homeodomain Proteins/genetics
  • Homeodomain Proteins/metabolism
  • Motor Neurons/drug effects*
  • Spinal Cord/drug effects
  • Spinal Cord/metabolism
  • Tubulin/metabolism
  • Water Pollutants, Chemical/toxicity*
  • Zebrafish/abnormalities
  • Zebrafish/embryology*
  • Zebrafish Proteins/genetics
  • Zebrafish Proteins/metabolism
PubMed: 21298338 Full text @ Ecotoxicology
ABSTRACT
Perfluorooctane sulfonate (PFOS) is an environmental organic pollutant, the potential neurotoxicity of which is causing great concern in fish. In the present study, we examined the effects of PFOS on motor neurons, and investigated the potential toxicological mechanisms oxidative stress in zebrafish embryos. Six-hour post-fertilization (hpf) zebrafish embryos were exposed to 1.0 mg/L PFOS, then we examined the expression of alpha-tubulin, proliferating cell nuclear antigen (PCNA), cyclin-dependent kinase 5 (CDK5), and peroxiredoxin 2 (PRX2) after PFOS exposure until 120 hpf. The results showed that PFOS increased alpha-tubulin in the coccygeal spinal cord (CSC) at 96 hpf, whereas decreased alpha-tubulin in the brain and spinal cord at 120 hpf. PCNA expression was highly increased in CSC and abdomen compared with control at 96 and 120 hpf after PFOS exposure. In addition, PFOS exposure caused CDK5 expression to be highly increased in brain region following by down-regulation of PRX2 expression at 96 hpf. These results indicated that, at least in part, the effect on motor neurons induced by PFOS was mediated by dynamically interfering with the expression of alpha-tubulin and PCNA. Furthermore, PFOS-induced toxicity was associated with oxidative stress by deregulating CDK5 and PRX2.
ADDITIONAL INFORMATION