Proinflammatory Cytokines in the Course ofMycobacteriumtuberculosis–Induced Apoptosis in Monocytes/Macrophages
Author(s) -
Antonio Ciaramella,
A. Cavone,
Marilina B. Santucci,
Massimo Amicosante,
Angelo Martino,
Giovanni Auricchio,
Leopoldo Paolo Pucillo,
Vittorio Colizzi,
Maurizio Fraziano
Publication year - 2002
Publication title -
the journal of infectious diseases
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.69
H-Index - 252
eISSN - 1537-6613
pISSN - 0022-1899
DOI - 10.1086/344645
Subject(s) - proinflammatory cytokine , apoptosis , tumor necrosis factor alpha , annexin , cytokine , biology , caspase 1 , mycobacterium tuberculosis , programmed cell death , immunology , microbiology and biotechnology , chemistry , inflammation , medicine , tuberculosis , pathology , biochemistry
Mycobacterium tuberculosis (MTB) can induce apoptosis in monocytes/macrophages both in vitro and in vivo, and this phenomenon is associated with mycobacterial survival. The present study addresses the possibility that apoptotic and inflammatory pathways could coexist through a caspase-1-mediated mechanism. In this context, a caspase-1 inhibitor (YVAD), but not caspase-3 (DEVD) or caspase-4 (LEVD) inhibitors, was able to strongly inhibit MTB-induced apoptosis. Moreover, caspase-1 activity was confirmed by the increased maturation of interleukin (IL)-1beta. Of interest, IL-1beta and tumor necrosis factor (TNF)-alpha were produced massively in the course of infection, and both were inhibited by YVAD pretreatment. To determine whether TNF-alpha was produced actively by apoptotic cells, the intracytoplasmatic cytokine content and apoptotic phenotype were analyzed at the single-cell level. Results showed a progressive increase of TNF-alpha production in annexin V-positive cells. These results indicate that MTB-induced apoptosis is associated with proinflammatory cytokine production.
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