Role of extracellular signal-regulated protein kinases in apoptosis by asbestos and H2O2

Author:

Jiménez Luis Albert1,Zanella Christine1,Fung Hua1,Janssen Yvonne M. W.1,Vacek Pam2,Charland Colette3,Goldberg Jonathan1,Mossman Brooke T.1

Affiliation:

1. Departments of Pathology,

2. Biostatistics, and

3. Medicine, College of Medicine, University of Vermont, Burlington, Vermont 05405

Abstract

Stimulation of cell signaling cascades by oxidants may be important in the pathogenesis of pulmonary and pleural diseases. Here, we demonstrate in rat pleural mesothelial cells that apoptotic concentrations of crocidolite asbestos and H2O2induce phosphorylation and activation of extracellular signal-regulated protein kinases (ERK). Activation of c- jun-NH2-terminal protein kinases (JNK)/stress-activated protein kinases was also observed in response to H2O2. In contrast, asbestos caused more protracted activation of ERK without JNK activation. Both H2O2- and asbestos-induced activation of ERK was abolished by catalase. Moreover, chelation of surface iron from crocidolite fibers or addition of N-acetyl-l-cysteine prevented ERK activation and apoptosis by crocidolite, indicating an oxidative mechanism of cell signaling. The MEK1 inhibitor PD-98059 abrogated asbestos-induced apoptosis, confirming a causal relationship between ERK activation and apoptosis. These results suggest that distinct cell-signaling cascades may be important in phenotypic responses elicited by oxidant stresses.

Publisher

American Physiological Society

Subject

Cell Biology,Physiology (medical),Pulmonary and Respiratory Medicine,Physiology

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