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Comparative effects of My cobacterium avium glycopeptidolipid and lipopeptide fragment on the function and ultrastructure of mononuclear cells.

Authors :
Pourshafie, M
Ayub, Q.
Barrow, W. W.
Source :
Clinical & Experimental Immunology. Jul1993, Vol. 93 Issue 1, p72-79. 8p.
Publication Year :
1993

Abstract

Among the various lipids associated with the cell envelope of the Mycabacterium avium complex, the species-specific glycopeplidolipids (GPL) are responsible for distinguishing one serovar from another. In a continuing effort to study the immunomodulatory capabilities of these mycobacterial lipids, we have examined and compared the effects of the GPL and its lipopeptide fragment (β-lipid) on mononuclear cell function. It was observed that the lymphoproliferative response of murine splenic mononuclear cells lo mitogen stimulation was reduced by both the GPL and its lipopeptide fragment. Although the responsiveness appeared lo be down-regulated to a greater degree by the (β-lipid, treatment with either GPL or β-lipid resulted in the release of soluble factors from peritoneal macrophages that caused suppression of the lymphoproliferative responsiveness of splenic mononuclear cells. Flow cylometric analysis of peritoneal macrophages revealed that treatment with the β-lipid fragment caused a marked decrease in expression of the C3bi complement receptor, Mac-1, on maerophages. whereas treatment with GPL resulted in a marked increase in the expression of Mac-2 receptor on maerophages. Treatment of peritoneal macrophages with either GPL or β-lipid resulted in the release of tumour necrosis factor (TNF), as determined by an L929 biological cytotoxicity assay. Perturbation of macrophage membrane ultrastructure by both GPL and β-lipid was confirmed by electron microscopy, and may be a possible explanation for the resulting alterations in mononuclear cell function observed in this study. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00099104
Volume :
93
Issue :
1
Database :
Academic Search Index
Journal :
Clinical & Experimental Immunology
Publication Type :
Academic Journal
Accession number :
15996265
Full Text :
https://doi.org/10.1111/1365-2249.ep15996265