Chlorination of ortho-position on Polychlorinated Biphenyls Increases Protein Kinase C Activity in Neuronal Cells.
- Author:
Youn Ju LEE
1
;
Jae Ho YANG
Author Information
1. Department of Pharmacology and Toxicology, School of Medicine, Catholic University of Daegu, Daegu 705-718, Korea. yangjh@cu.ac.kr
- Publication Type:Original Article
- Keywords:
Polychlorinated biphenyls;
Protein kinase C;
Cerebellar granule cell;
ROS;
AhR;
Structure-activity relationship
- MeSH:
Antibodies, Monoclonal;
Cell Culture Techniques;
Cytosol;
Environmental Pollutants;
Halogenation;
Isoenzymes;
Learning;
Membranes;
Memory;
Neurons;
Phorbols;
Polychlorinated Biphenyls;
Protein Kinase C;
Protein Kinases;
Structure-Activity Relationship
- From:Toxicological Research
2012;28(2):107-112
- CountryRepublic of Korea
- Language:English
-
Abstract:
Polychlorinated biphenyls (PCBs) are persistent and bioaccumulative environmental pollutants. Recently, it is suggested that neurotoxic effects such as motor dysfunction and impairment in memory and learning have been associated with PCB exposure. However, structure relationship of PCB congeners with neurotoxic effects remains unknown. Since PKC signaling pathway is implicated in the modulation of motor behavior as well as learning and memory and the role of PKC are subspecies-specific, we attempted to study the effects of structurally distinct PCBs on the total PKC activity as well as subspecies of PKC in cerebellar granule cell culture model. Cells were exposed to 0, 25 and 50 microM of PCB-126, PCB-169, PCB-114, PCB-157, PCB-52 and PCB-4 for 15 min. Cells were subsequently analyzed by [3H] phorbol ester binding assay or immunoblotted against PKC-alpha and -epsilon monoclonal antibodies. While non-dioxin-like-PCB (PCB-52 and PCB-4) induced a translocation of PKC-alpha and -epsilon from cytosol to membrane fraction, dioxin-like PCBs (PCB-126, -169, -114, -157) had no effects. [3H] Phorbol ester binding assay also revealed structure-dependent increase similar to translocation of PKC isozymes. While PCB-4 induced translocation of PKC-alpha and -epsilon was inhibited by ROS inhibitor, the pattern of translocation was not affected in presence of AhR inhibitor. It is suggested that PCB-4-induced PKC activity may not be mediated via AhR-dependent pathway. Taken together, our findings suggest that chlorination of ortho-position in PCB may be a critical structural moiety associated with neurotoxic effects, which may be preferentially mediated via non-AhR-dependent pathway. Therefore, the present study may contribute to understanding the neurotoxic mechanism of PCBs as well as providing a basis for establishing a better neurotoxic assessment.
