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Activation of extracellular signal‐regulated kinases (ERK 44/42) by chlorpyrifos oxon in Chinese hamster ovary cells
Author(s) -
Bomser Joshua,
Casida John E.
Publication year - 2000
Publication title -
journal of biochemical and molecular toxicology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.526
H-Index - 58
eISSN - 1099-0461
pISSN - 1095-6670
DOI - 10.1002/1099-0461(2000)14:6<346::aid-jbt7>3.0.co;2-h
Subject(s) - mapk/erk pathway , wortmannin , kinase , protein kinase c , chinese hamster ovary cell , signal transduction , protein kinase a , microbiology and biotechnology , chemistry , biology , biochemistry , phosphatidylinositol , receptor
Abstract Acetylcholinesterase inhibition explains most but not all of the toxicological manifestations of exposure to the major organophosphorus insecticide chlorpyrifos (CP) and its metabolically activated form chlorpyrifos oxon (CPO); CPO is also reported to interact with muscarinic acetylcholine receptors and alter secondary messenger status. We find that CP and CPO activate extracellular signal‐regulated kinases (ERK 44/42) in both wild‐type (CHOK1) and human muscarinic receptor‐expressing Chinese hamster ovary cells (CHO‐M2). The degree of ERK 44/42 activation on treatment with 50 μM CPO for 40 minutes is 2‐ to 3‐fold compared with control cells and is both concentration‐ and time‐dependent. CP is at least 2‐fold less potent than CPO as an activator of ERK 44/42 and the hydrolysis products 3,5,6‐trichloropyridinol and diethyl phosphate are not activators. ERK 44/42 activation by CPO is insensitive to the protein kinase A inhibitor H‐89, but is completely abolished by the phosphatidylinositol 3‐kinase (P13‐K) inhibitor wortmannin, the protein kinase C (PKC) inhibitor GF‐109203X, and the mitogen‐activated extracellular signal‐regulated protein kinase kinase (MEK) inhibitor PD 098059. Therefore, CPO activates the ERK 44/42 signaling cascade in CHOK1 cells via a pathway dependent on P13‐K, PKC, and MEK but not requiring PKA or the human M2 muscarinic receptor. In summary we find that CPO activates a mammalian signal transduction cascade involved in cell growth and differentiation. This occurs through a pathway common to growth factors and mitogens, consistent with a receptor‐mediated event. However, CPO may also inhibit an enzyme involved in signal transduction. The specific target of CPO leading to the activation of ERK 44/42 and the potential effects of this activation on cell function remain to be determined. © 2000 John Wiley & Sons, Inc. J Biochem Mol Toxicol 14:346–353, 2000

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