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Differential induction of c-fos, c-jun, and apoptosis in lung epithelial cells exposed to ROS or RNS.

Authors
Janssen-YM; Matalon-S; Mossman-BT
Source
Am J Physiol, Lung Cell Mol Physiol 1997 Oct; 273(4):L789-L796
NIOSHTIC No.
00241854
Abstract
Induction of c-fos and c-jun gene expression and apoptosis by reactive oxygen species (ROS) and reactive nitrogen species (RNS) in lung epithelial cells was demonstrated. RLE-6TN cells, a rat lung type II epithelial cell line, were exposed to 0 to 1 millimolar (mM) hydrogen-peroxide (7722841), nitric-oxide (10102439), or peroxynitrite (26404660) for 2 hours. Peroxynitrite was produced exogenously by reacting hydrogen-peroxide with sodium-nitrite or generated in-situ from 3-morpholinosydnonimine. Nitric-oxide was generated in-situ from spermine-1,3-propanediamine-N-(4-(1-(3- aminopropyl)-2- hydroxy-2-nitrosohydrazino)-butyl) or from S-nitro-N- acetylpenicillamine. The RNA was extracted from some cells and the level of expression of c-fos and c-jun mRNA was determined by Northern blotting. The concentrations of c-fos and c-jun proteins was determined by Western blotting. The extent of binding of activator-protein-1-transcription-factor (AP-1-TF) to AP-1 consensus DNA sequences was measured by an electrophoresis mobility shift assay. Induction of apoptosis was evaluated by a flow cytometric assay based on identifying cells with hypodiploid DNA and by a DNA laddering assay. Nitric-oxide and hydrogen-peroxide significantly increased the level of c-fos and c-jun mRNA expression, c-fos and c- jun protein concentrations, level of AP-1-TF binding to AP-1 consensus DNA sequences, and cellular apoptosis. Peroxynitrite applied exogenously to the cells or that was generated in-situ had no significant effect on these parameters. The authors conclude that nitric-oxide or hydrogen-peroxide increases early response gene expression leading to apoptosis in lung epithelial cells. Peroxynitrite did not cause these effects. Induction of c-fos and c- jun transcripts by ROS and RNS may play a critical role in the development of pulmonary diseases which are associated with reactive metabolites.
Keywords
NIOSH-Publication; NIOSH-Grant; Pulmonary-system-disorders; Lung-cells; Genetics; Oxidative-processes; Nitrogen-oxides; In-vitro-studies; Cell-damage; Nucleic-acids; Peroxides
CODEN
APLPE7
CAS No.
7722-84-1; 10102-43-9; 26404-66-0
Publication Date
19971001
Document Type
Journal Article
Funding Amount
75969
Funding Type
Grant
Fiscal Year
1998
NTIS Accession No.
NTIS Price
Identifying No.
Grant-Number-R03-OH-03467
Issue of Publication
4
ISSN
1040-0605
Source Name
American Journal of Physiology: Lung Cellular and Molecular Physiology
State
VT
Performing Organization
Pathology University of Vermont Medical Alumni Bldg a 249 Burlington, VT 05405-0068
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