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Antigen activation of THP‐1 human monocytic cells after stimulation with lipopolysaccharide from oral microorganisms and granulocyte‐macrophage colony‐stimulating factor
Author(s) -
Baqui A. A. M. A.,
Meiller Timothy F.,
Kelley Jacqueline I.,
Turng BeenFoo,
Falkler William A.
Publication year - 1999
Publication title -
journal of periodontal research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.31
H-Index - 83
eISSN - 1600-0765
pISSN - 0022-3484
DOI - 10.1111/j.1600-0765.1999.tb02243.x
Subject(s) - thp1 cell line , fusobacterium nucleatum , antigen , lipopolysaccharide , porphyromonas gingivalis , monocyte , microbiology and biotechnology , immune system , macrophage , cell culture , biology , chemistry , immunology , in vitro , biochemistry , bacteria , genetics
A human THP‐1 monocyte cell line culture system has been utilized to evaluate the morphological changes in THP‐1 cells and to measure expression of activation antigens (CD‐11b, CD‐11c, CD‐14, CD‐35, CD‐68, CD‐71 and HLA‐DR) as evidence of maturation of THP‐1 cells in response to stimulation by lipopolysaccharide (LPS) from the oral microorganisms, Fusobacterium nucleatum and Porphyromonas gingivalis , and granulocyte‐macrophage colony‐stimulating factor. THP‐1 cells were stimulated with LPS (1 μg/ml) of P. gingivalis or F. nucleatum for different time periods (1, 2, 4 and 7 d). Detection of different activation antigens on THP‐1 cells was performed by indirect immunohistochemical staining followed by light microscopy. Confirmational studies were performed in parallel using indirect immunofluorescence and immunogold electron microscopy for detection of the corresponding activation antigens. Expression of different activation antigens by resting THP‐1 cells revealed HLA‐DR to be on 3% of the cells; CD‐11b, 9%; CD‐11c, 8%; CD‐14, 22%; CD‐35, 9% and CD‐68, 7%. The CD‐71 activation antigen was not expressed in untreated THP‐1 cells. LPS stimulation increased expression of all activation antigens. A significant ( p < 0.05) increase in expression of CD‐11b, CD‐11c, CD‐14, CD‐35, CD‐68 and CD‐71 was observed when GM‐CSF (50 IU/ml) was supplemented during the treatment of THP‐1 cells with LPS of F. nucleatum or P. gingivalis. Activation and differentiation of THP‐1 cells by LPS from oral microorganisms in the presence of GM‐CSF supports a role for human macrophages in acute and chronic periodontal diseases and may explain the clinically observable periodontal exacerbations in some patients after GM‐CSF therapy.