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Role of bioavailable iron in coal dust-induced activation of activator protein-1 and nuclear factor of activated T cells: difference between Pennsylvania and Utah coal dusts.

Authors
Huang-C; Li-J; Zhang-Q; Huang-X
Source
Am J Respir Cell Mol Biol 2002 Nov; 27(5):568-574
NIOSHTIC No.
20029527
Abstract
Activator protein-1 (AP-1) and nuclear factor of activated T cells (NFAT) are two important transcription factors responsible for the regulation of cytokines, which are involved in cell proliferation and inflammation. Coal workers' pneumoconiosis (CWP) is an occupational lung disease that may be related to chronic inflammation caused by coal dust exposure. In the present study, we demonstrate that coal from the Pennsylvania (PA) coalmine region, which has a high prevalence of CWP, can activate both AP-1 and NFAT in JB6 mouse epidermal cells. In contrast, coal from the Utah (UT) coalmine region, which has a low prevalence of CWP, has no such effects. The PA coal stimulates mitogen-activated protein kinase (MAPK) family members of extracellular signal-regulated kinases (ERKs) and p38 MAPK but not c-Jun-NH(2)-terminal kinases, as determined by the phosphorylation assay. The increase in AP-1 by the PA coal was completely eliminated by the pretreatment of cells with PD98059, a specific MAPK kinase inhibitor, and SB202190, a p38 kinase inhibitor, further confirming that the PA coal-induced AP-1 activation is mediated through ERKs and p38 MAPK pathways. Deferoxamine (DFO), an iron chelator, synergistically enhanced the PA coal-induced AP-1 activity, but inhibited NFAT activity. For comparison, cells were treated with ferrous sulfate and/or DFO. We have found that iron transactivated both AP-1 and NFAT, and DFO further enhanced iron-induced AP-1 activation but inhibited NFAT. These results indicate that activation of AP-1 and NFAT by the PA coal is through bioavailable iron present in the coal. These data are in agreement with our previous findings that the prevalence of CWP correlates well with levels of bioavailable iron in coals from various mining regions.
Keywords
Coal-workers; Coal-mining; Coal-miners; Lung-disease; Diseases; Coal-dust; Iron-compounds; Pulmonary-system-disorders; Respiratory-system-disorders; Pneumoconiosis
Contact
Department of Environmental Medicine, New York University School of Medicine, New York 10016
CODEN
AJRBEL
CAS No.
471-34-1
Publication Date
20021101
Document Type
Journal Article
Email Address
xihuang@env.med.nyu.edu
Funding Amount
638746
Funding Type
Grant
Fiscal Year
2003
NTIS Accession No.
NTIS Price
Identifying No.
Grant-Number-R01-OH-003561
Issue of Publication
5
ISSN
1044-1549
Source Name
American Journal of Respiratory Cell and Molecular Biology
State
NY
Performing Organization
New York University Medical Center, New York, New York
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