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Chlorpyrifos affects phenotypic outcomes in a model of mammalian neurodevelopment: critical stages targeting differentiation in PC12 cells.

Publication ,  Journal Article
Jameson, RR; Seidler, FJ; Qiao, D; Slotkin, TA
Published in: Environ Health Perspect
May 2006

The organophosphate insecticide chlorpyrifos (CPF) adversely affects mammalian brain development through multiple mechanisms. To determine if CPF directly affects neuronal cell replication and phenotypic fate, and to identify the vulnerable stages of differentiation, we exposed PC12 cells, a model for mammalian neurodevelopment, to CPF concentrations spanning the threshold for cholinesterase inhibition (5-50 microM) and conducted evaluations during mitosis and in early and mid-differentiation. In undifferentiated cells, exposure to 5 microM CPF for 1-3 days reduced DNA synthesis significantly without eliciting cytotoxicity. At the same time, CPF increased the expression of tyrosine hydroxylase (TH), the enzymatic marker for the catecholamine phenotype, without affecting choline acetyltransferase (ChAT), the corresponding marker for the cholinergic phenotype. Upon exposure to nerve growth factor (NGF), PC12 cells developed neuritic projections in association with vastly increased TH and ChAT expression accompanying differentiation into the two phenotypes. CPF exposure begun at the start of differentiation significantly reduced ChAT but not TH activity. In contrast, when CPF was added in mid-differentiation (4 days of NGF pretreatment), ChAT was unaffected and TH was increased slightly. Thus, CPF exerts stage-specific effects, reducing DNA synthesis in the undifferentiated state, impairing development of the cholinergic phenotype at the start of differentiation, and promoting expression of the catecholaminergic phenotype both in undifferentiated and differentiated cells. CPF administration in vivo produces deficits in the number of neurons and cholinergic function, and because we were able to reproduce these effects in vitro, our results suggest that CPF directly influences the phenotypic fate of neuronal precursors.

Duke Scholars

Published In

Environ Health Perspect

DOI

ISSN

0091-6765

Publication Date

May 2006

Volume

114

Issue

5

Start / End Page

667 / 672

Location

United States

Related Subject Headings

  • Tyrosine 3-Monooxygenase
  • Toxicology
  • Rats
  • Physostigmine
  • Pesticides
  • PC12 Cells
  • Neurons
  • Nerve Growth Factor
  • Dose-Response Relationship, Drug
  • Cholinesterase Inhibitors
 

Citation

APA
Chicago
ICMJE
MLA
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Jameson, R. R., Seidler, F. J., Qiao, D., & Slotkin, T. A. (2006). Chlorpyrifos affects phenotypic outcomes in a model of mammalian neurodevelopment: critical stages targeting differentiation in PC12 cells. Environ Health Perspect, 114(5), 667–672. https://doi.org/10.1289/ehp.8750
Jameson, Ruth R., Frederic J. Seidler, Dan Qiao, and Theodore A. Slotkin. “Chlorpyrifos affects phenotypic outcomes in a model of mammalian neurodevelopment: critical stages targeting differentiation in PC12 cells.Environ Health Perspect 114, no. 5 (May 2006): 667–72. https://doi.org/10.1289/ehp.8750.
Jameson RR, Seidler FJ, Qiao D, Slotkin TA. Chlorpyrifos affects phenotypic outcomes in a model of mammalian neurodevelopment: critical stages targeting differentiation in PC12 cells. Environ Health Perspect. 2006 May;114(5):667–72.
Jameson, Ruth R., et al. “Chlorpyrifos affects phenotypic outcomes in a model of mammalian neurodevelopment: critical stages targeting differentiation in PC12 cells.Environ Health Perspect, vol. 114, no. 5, May 2006, pp. 667–72. Pubmed, doi:10.1289/ehp.8750.
Jameson RR, Seidler FJ, Qiao D, Slotkin TA. Chlorpyrifos affects phenotypic outcomes in a model of mammalian neurodevelopment: critical stages targeting differentiation in PC12 cells. Environ Health Perspect. 2006 May;114(5):667–672.

Published In

Environ Health Perspect

DOI

ISSN

0091-6765

Publication Date

May 2006

Volume

114

Issue

5

Start / End Page

667 / 672

Location

United States

Related Subject Headings

  • Tyrosine 3-Monooxygenase
  • Toxicology
  • Rats
  • Physostigmine
  • Pesticides
  • PC12 Cells
  • Neurons
  • Nerve Growth Factor
  • Dose-Response Relationship, Drug
  • Cholinesterase Inhibitors