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Clinical and Diagnostic Laboratory Immunology, May 1998, p. 341-347, Vol. 5, No. 3
Department of Oral
Medicine1 and
Department of
OCBS,2 Dental School, University of
Maryland, Baltimore, Maryland
Received 1 October 1997/Returned for modification 20 November
1997/Accepted 16 February 1998
Cytokines, including granulocyte-macrophage colony-stimulating
factor (GM-CSF), are used to assist in bone marrow recovery during
cancer chemotherapy. Interleukin-1
1071-412X/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
Granulocyte-Macrophage Colony-Stimulating Factor
Amplification of Interleukin-1
and Tumor Necrosis Factor Alpha
Production in THP-1 Human Monocytic Cells Stimulated with
Lipopolysaccharide of Oral Microorganisms
(IL-1
) and tumor necrosis factor alpha (TNF-
) play important roles in inflammatory processes, including exacerbation of periodontal diseases, one of the most common
complications in patients who undergo this therapy. A human monocyte
cell line (THP-1) was utilized to investigate IL-1
and TNF-
production following GM-CSF supplementation with lipopolysaccharide (LPS) from two oral microorganisms, Porphyromonas
gingivalis and Fusobacterium nucleatum. LPS of
P. gingivalis or F. nucleatum was prepared by a
phenol-water extraction method and characterized by sodium dodecyl
sulfate-polyacrylamide gel electrophoresis and determination of total
protein and endotoxin contents. Resting THP-1 cells were treated with
LPS of P. gingivalis or F. nucleatum and/or
GM-CSF (50 IU/ml) by using different concentrations for various time
periods. Production of IL-1
and TNF-
in THP-1 cells was measured
by solid-phase enzyme-linked immunosorbent assay. Reverse transcription
(RT)-PCR was used to evaluate the gene expression of resting and
treated THP-1 cells. IL-1
was not detected in untreated THP-1 cells.
IL-1
production was, however, stimulated sharply at 4 h. GM-CSF
amplified IL-1
production in THP-1 cells treated with LPS from both
oral anaerobes. No IL-1
-specific mRNA transcript was detected in
untreated THP-1 cells. However, IL-1
mRNA was detected by RT-PCR
2 h after stimulation of THP-1 cells with LPS from both organisms.
GM-CSF did not shorten the IL-1
transcriptional activation time.
GM-CSF plus F. nucleatum or P. gingivalis LPS
activated THP-1 cells to produce a 1.6-fold increase in TNF-
production at 4 h over LPS stimulation alone. These investigations with the in vitro THP-1 model indicate that there may be an increase in
the cellular immune response to oral endotoxin following GM-CSF therapy, as evidenced by production of the tissue-reactive cytokines IL-1
and TNF-
.
*
Corresponding author. Mailing address: Department of
Oral Medicine, Dental School, UMAB, 666 W. Baltimore Street, Baltimore, MD 21201. Phone: (410) 708-7628. Fax: (410) 706-0519. E-mail: aab001{at}dental.umaryland.edu.
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