Document Detail


Effect of acidosis on IL-8 and MCP-1 during hypoxia and reoxygenation in human NT2-N neurons.
MedLine Citation:
PMID:  16919250     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Inflammation probably plays a significant role in perinatal brain injury. To study the contribution of locally produced cytokines, the effect on cell death of addition of IL-8 and MCP-1 or antibodies to these, and the impact of acidosis, human postmitotic NT2-N neurons were exposed to 3 h of hypoxia and glucose deprivation and reoxygenated for 21 h. After 3 h of hypoxia with neutral medium, IL-8 was significantly increased compared to controls (150 (100-250)% vs. 100 (85-115)%, p=0.023). After 21 h of neutral reoxygenation, both IL-8 (380 (110-710)% vs. 150 (85-260)%, p=0.041) and monocyte chemoattractant protein-1 (MCP-1) (650 (440-2000)% vs. 310 (230-340)%, p=0.007) were significantly increased compared to controls. After 3 h of hypoxia, both IL-8 (p=0.002) and MCP-1 (p=0.008) were significantly lower in cells with acidotic compared with cells with neutral medium. Acidosis during reoxygenation, however, significantly increased IL-8 release, whereas MCP-1 release was diminished. Similar effects of acidosis were seen in normoxic controls. The cells also secreted RANTES and IP-10, but not 8 other cytokines tested. We found no effect on cell death, measured by MTT assay, of addition of IL-8, MCP-1 or antibodies to these. We conclude that human NT2-N neurons release IL-8 and MCP-1 during 21 h of reoxygenation after 3 h of hypoxia. Acidosis led to a differential effect on IL-8 and MCP-1, with increased IL-8 and decreased MCP-1, both during reoxygenation and in normoxic controls. IL-8 and MCP-1 had no effect on cell death.
Authors:
Elisabeth Frøyland; Elena Didenko Pedersen; Anne-Katrine Kvissel; Runar Almaas; Anne Pharo; Bjørn Steen Skålhegg; Tom Eirik Mollnes; Terje Rootwelt
Publication Detail:
Type:  Comparative Study; Journal Article; Research Support, Non-U.S. Gov't     Date:  2006-08-17
Journal Detail:
Title:  Brain research     Volume:  1113     ISSN:  0006-8993     ISO Abbreviation:  Brain Res.     Publication Date:  2006 Oct 
Date Detail:
Created Date:  2006-09-25     Completed Date:  2006-12-13     Revised Date:  2007-11-15    
Medline Journal Info:
Nlm Unique ID:  0045503     Medline TA:  Brain Res     Country:  Netherlands    
Other Details:
Languages:  eng     Pagination:  64-73     Citation Subset:  IM    
Affiliation:
Department of Pediatric Research, Rikshospitalet-Radiumhospitalet Medical Center and University of Oslo, N-0027 Oslo, Norway. elisabeth.froyland@medisin.uio.no
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MeSH Terms
Descriptor/Qualifier:
Acidosis / metabolism*
Anoxia
Antibodies / pharmacology
Cell Hypoxia / physiology
Cell Line
Chemokine CCL2 / immunology,  metabolism*
Chemokine CCL5 / metabolism
Dose-Response Relationship, Drug
Fluorescent Antibody Technique / methods
Gene Expression Regulation / drug effects*
Glucose / deficiency
Humans
Interleukin-8 / immunology,  metabolism*
Neurofilament Proteins / metabolism
Neurons / physiology*
Oxygen / administration & dosage*
Statistics, Nonparametric
Tetrazolium Salts / diagnostic use
Thiazoles / diagnostic use
Time Factors
Chemical
Reg. No./Substance:
0/Antibodies; 0/Chemokine CCL2; 0/Chemokine CCL5; 0/Interleukin-8; 0/Neurofilament Proteins; 0/Tetrazolium Salts; 0/Thiazoles; 108688-71-7/neurofilament protein H; 298-93-1/thiazolyl blue; 50-99-7/Glucose; 7782-44-7/Oxygen

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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