Document Detail


Benzo[a]pyrene impairs neurodifferentiation in PC12 cells.
MedLine Citation:
PMID:  19539729     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Animal studies indicate neurobehavioral anomalies after prenatal exposure to benzo[a]pyrene (BaP). In order to determine if BaP directly affects neurodevelopment, we compared its effects to those of the organophosphate insecticide, chlorpyrifos (CPF), in undifferentiated and differentiating neuronotypic PC12 cells, evaluating indices of cell replication, cell number, neurite outgrowth and phenotypic differentiation. Unlike CPF, BaP did not inhibit DNA synthesis in undifferentiated cells. In cells undergoing nerve growth factor-induced differentiation, CPF reduced cell numbers (assessed by DNA content) whereas BaP increased them, suggesting a delay in the transition between cell replication and differentiation. Indices of cell enlargement (total protein/DNA) and neurite outgrowth (membrane protein/DNA) also showed opposite effects of CPF (increases) and BaP (decreases). We directly confirmed BaP impairment of neurodifferentiation by measuring markers for the two neurotransmitter phenotypes expressed by PC12 cells: tyrosine hydroxylase (dopamine phenotype) and choline acetyltransferase (acetylcholine phenotype). BaP significantly reduced both markers in differentiating cells, with a preferentially greater effect on the acetylcholine phenotype. Our results indicate that low, non-toxic levels of BaP can impair neurodifferentiation, resulting in excess cell numbers at the expense of the emergence of neurotransmitter phenotypes. BaP thus has direct actions on developing neuronal cells that could contribute to the adverse neurodevelopmental effects seen with in vivo exposures.
Authors:
Theodore A Slotkin; Frederic J Seidler
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Publication Detail:
Type:  Journal Article; Research Support, N.I.H., Extramural     Date:  2009-06-17
Journal Detail:
Title:  Brain research bulletin     Volume:  80     ISSN:  1873-2747     ISO Abbreviation:  Brain Res. Bull.     Publication Date:  2009 Aug 
Date Detail:
Created Date:  2009-07-27     Completed Date:  2009-11-02     Revised Date:  2010-09-27    
Medline Journal Info:
Nlm Unique ID:  7605818     Medline TA:  Brain Res Bull     Country:  United States    
Other Details:
Languages:  eng     Pagination:  17-21     Citation Subset:  IM    
Affiliation:
Department of Pharmacology and Cancer Biology, Duke University Medical Center, Durham, NC 27710, USA. t.slotkin@duke.edu
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MeSH Terms
Descriptor/Qualifier:
Animals
Benzo(a)pyrene / pharmacology*
Cell Differentiation / drug effects*
Chlorpyrifos / pharmacology
Choline O-Acetyltransferase / metabolism
Cholinesterase Inhibitors / pharmacology
Dose-Response Relationship, Drug
Humans
Insecticides / pharmacology
PC12 Cells* / drug effects,  physiology
Rats
Tyrosine 3-Monooxygenase / metabolism
Grant Support
ID/Acronym/Agency:
ES10356/ES/NIEHS NIH HHS; P42 ES010356-090001/ES/NIEHS NIH HHS
Chemical
Reg. No./Substance:
0/Cholinesterase Inhibitors; 0/Insecticides; 2921-88-2/Chlorpyrifos; 50-32-8/Benzo(a)pyrene; EC 1.14.16.2/Tyrosine 3-Monooxygenase; EC 2.3.1.6/Choline O-Acetyltransferase
Comments/Corrections

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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