Suppression of metalloproteinase biosynthesis in human alveolar macrophages by interleukin-4.

Détails

ID Serval
serval:BIB_7F1EE5A6ECE1
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Titre
Suppression of metalloproteinase biosynthesis in human alveolar macrophages by interleukin-4.
Périodique
Journal of Clinical Investigation
Auteur(s)
Lacraz S., Nicod L., Galve-de Rochemonteix B., Baumberger C., Dayer J.M., Welgus H.G.
ISSN
0021-9738[print], 0021-9738[linking]
Statut éditorial
Publié
Date de publication
1992
Volume
90
Numéro
2
Pages
382-388
Langue
anglais
Résumé
To study the interaction of lymphocytes and macrophages in the control of extracellular matrix turnover, we determined the effects of several soluble T cell products on mononuclear phagocyte production of metalloproteinases. Cytokines including IL-2, IL-4, IL-6, tumor necrosis factor alpha (TNF alpha), GM-CSF, and IFN-gamma were each tested for capacity to modulate macrophage metalloproteinase and tissue inhibitor of metalloproteinases (TIMP) expression. The addition of IL-4 to cells cultured under basal conditions caused a dose-dependent suppression in the release of 92-kD type IV collagenase without affecting TIMP production. 92-kD enzyme secretion was inhibited by 50% with 1-2 ng/ml of IL-4 and by 90% with 10 ng/ml of IL-4. When cells were first exposed to killed Staphylococcus aureus to induce metalloproteinase production, IL-4 potently blocked the stimulated release of both interstitial collagenase and 92-kD type IV collagenase, again without effect upon TIMP. Metabolic labeling experiments and Northern hybridizations demonstrated that IL-4 exerted its action at a pretranslational level. Furthermore, IL-4 possessed the capacity to inhibit metalloproteinase expression even in the relatively immature peripheral blood monocyte. As reported previously (Shapiro, S. D., E. J. Campbell, D. K. Kobayashi, and H. G. Welgus. 1990. J. Clin. Invest. 86:1204), IFN-gamma suppressed constitutive macrophage production of 92-kD type IV collagenase. Despite the frequent antagonism observed between IL-4 and IFN-gamma in other systems, the combination of these two agents lowered metalloproteinase biosynthesis dramatically, whereas IL-4 opposed the IFN-gamma-stimulated production of cytokines (IL-1 and TNF alpha). IL-6 had only minimal effect upon metalloproteinase production, but appeared to specifically augment TIMP release. In summary, cytokines released by activated T cells may profoundly reduce the capacity of the macrophage to mediate extracellular matrix degradation.
Mots-clé
Gene Expression/drug effects, Glycoproteins/secretion, Humans, Interferon-gamma/pharmacology, Interleukin-1/biosynthesis, Interleukin-4/pharmacology, Macrophage Activation, Macrophages, Alveolar/enzymology, Metalloendopeptidases/biosynthesis, Metalloendopeptidases/genetics, Microbial Collagenase/secretion, RNA, Messenger/genetics, Tissue Inhibitor of Metalloproteinases, Tumor Necrosis Factor-alpha/pharmacology
Pubmed
Web of science
Création de la notice
19/02/2010 19:10
Dernière modification de la notice
03/03/2018 18:42
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