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PMID: 7546769 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Alterations of ambient oxygen tension modulate the expression of tumor necrosis factor and macrophage inflammatory protein-1 alpha from murine alveolar macrophages.

American journal of respiratory cell and molecular biology ·Vol. 13 ·No. 4 ·1995-10-00 ·Pages 399-409

VanOtteren GM, Standiford TJ, Kunkel SL, Danforth JM, Strieter RM

Abstract

Tissue injury that occurs as a result of ischemia and subsequent reperfusion is characterized by endothelial cell injury, edema formation, and the influx of inflammatory leukocytes. Two macrophage-derived proinflammatory cytokines which may play a critical role in cellular injury and leukocyte recruitment/activation that occurs in the setting of ischemia-reperfusion injury are tumor necrosis factor alpha (TNF) and macrophage inflammatory protein-1 alpha (MIP-1 alpha). To determine if modulation of ambient oxygen tensions in vitro alters the expression of proinflammatory cytokines from activated macrophages, murine alveolar macrophages (AMO) were cultured in various combinations of ambient oxygen concentrations, then the supernatant fluid and cell pellet assayed for the presence of TNF and MIP-1 alpha messenger RNA (mRNA) and protein. We demonstrated that conditions of anoxia (95% nitrogen/5% CO2) or hyperoxia (95% oxygen/5% CO2) independently resulted in the increased expression of both TNF and MIP-1 alpha mRNA and protein from lipopolysaccharide (LPS)-stimulated AMO, as compared with cells cultured in room air. The specific culture condition of anoxia (x 6 h) followed by hyperoxia (x 18 h) produced the greatest increases in both TNF and MIP-1 alpha, suggesting that when following a period of anoxic priming, oxygen stress results in exaggerated cytokine production. A period of at least 4.5 to 6 h of anoxia prior to hyperoxic exposure was found to be the minimal time required for anoxic priming. Furthermore, the coincubation of LPS-treated AMO with dimethyl sulfoxide (DMSO) attenuated the anoxia-hyperoxia-induced increases in TNF and MIP-1 alpha mRNA by 23% and 34%, respectively. These findings suggested that alterations in ambient oxygen tension can regulate the expression of TNF and MIP-1 alpha from activated AMO, and that oxidant-related cytokine production may represent an important mechanism by which inflammation occurs in the clinical settings of ischemia-reperfusion injury and hyperoxia.

MeSH Terms
Animals Base Sequence Cell Hypoxia Cells, Cultured Chemokine CCL4 Cytokines/biosynthesis Dimethyl Sulfoxide/pharmacology Female Free Radical Scavengers/pharmacology Gene Expression Regulation/drug effects Lipopolysaccharides/pharmacology Macrophage Activation Macrophage Inflammatory Proteins Macrophages, Alveolar/metabolism Mice Molecular Sequence Data Monokines/biosynthesis Oxidative Stress RNA, Messenger/biosynthesis Tumor Necrosis Factor-alpha/biosynthesis
Chemicals
Chemokine CCL4 Cytokines Free Radical Scavengers Lipopolysaccharides Macrophage Inflammatory Proteins Monokines RNA, Messenger Tumor Necrosis Factor-alpha Dimethyl Sulfoxide
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
VanOtteren G M
Department of Medicine, University of Michigan Medical School, Ann Arbor, USA.
Standiford T J
Kunkel S L
Danforth J M
Strieter R M
Article Info
Journal
American journal of respiratory cell and molecular biology
Abbr.
Am J Respir Cell Mol Biol
ISSN
1044-1549
Published
1995-10-00
Pages
399-409
Language
English
Region
United States
NLM ID
8917225
Subset
IM
Grants
NHLBI NIH HHS · HL50057 · United States
NHLBI NIH HHS · HL52800 · United States
NHLBI NIH HHS · IP50HL46487 · United States
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