Mycobacterium tuberculosis induces apoptosis in human monocyte-derived macrophages (MDMs) during the early stages of infection. We investigated the proapoptotic role of cell wall-associated mycobacterial 19-kDa lipoprotein and the possible association between 19-kDa lipoprotein signaling and production of proinflammatory cytokines. Purified mycobacterial 19-kDa lipoprotein, 19-kDa lipoprotein-expressing M. smegmatis (M. smegmatis 19+), 19-kDa lipoprotein knockout (KO) M. tuberculosis, and 19-kDa lipoprotein KO M. bovis bacille Calmette-Guerin (BCG) strains were analyzed for their ability to induce apoptosis in MDMs. The 19-kDa lipoprotein and infection with M. smegmatis 19+ induced apoptosis in MDMs. M. tuberculosis and BCG KO strains had significantly decreased abilities to induce apoptosis. The 19-kDa lipoprotein proapoptotic signal was mediated by Toll-like receptor 2 but not by tumor necrosis factor-alpha. Only the release of interleukin (IL)-1 beta was decreased after infection with 19-kDa lipoprotein KO strains. These findings indicate that the 19-kDa lipoprotein is the main signal required to trigger both apoptosis and the release of IL-1 beta during the early stages of mycobacterial infection.

Ciaramella, A., Cavone, A., Santucci, M.b., Garg, S., Sanarico, N., Bocchino, M., et al. (2004). Induction of apoptosis and release of interleukin-1 beta by cell wall-associated 19-kDa lipoprotein during the course of mycobacterial infection. THE JOURNAL OF INFECTIOUS DISEASES, 190(6), 1167-1176 [10.1086/423850].

Induction of apoptosis and release of interleukin-1 beta by cell wall-associated 19-kDa lipoprotein during the course of mycobacterial infection

SANTUCCI, MARILINA BENEDETTA;COLIZZI, VITTORIO;FRAZIANO, MAURIZIO
2004-09-15

Abstract

Mycobacterium tuberculosis induces apoptosis in human monocyte-derived macrophages (MDMs) during the early stages of infection. We investigated the proapoptotic role of cell wall-associated mycobacterial 19-kDa lipoprotein and the possible association between 19-kDa lipoprotein signaling and production of proinflammatory cytokines. Purified mycobacterial 19-kDa lipoprotein, 19-kDa lipoprotein-expressing M. smegmatis (M. smegmatis 19+), 19-kDa lipoprotein knockout (KO) M. tuberculosis, and 19-kDa lipoprotein KO M. bovis bacille Calmette-Guerin (BCG) strains were analyzed for their ability to induce apoptosis in MDMs. The 19-kDa lipoprotein and infection with M. smegmatis 19+ induced apoptosis in MDMs. M. tuberculosis and BCG KO strains had significantly decreased abilities to induce apoptosis. The 19-kDa lipoprotein proapoptotic signal was mediated by Toll-like receptor 2 but not by tumor necrosis factor-alpha. Only the release of interleukin (IL)-1 beta was decreased after infection with 19-kDa lipoprotein KO strains. These findings indicate that the 19-kDa lipoprotein is the main signal required to trigger both apoptosis and the release of IL-1 beta during the early stages of mycobacterial infection.
15-set-2004
Pubblicato
Rilevanza internazionale
Articolo
Sì, ma tipo non specificato
Settore MED/04 - PATOLOGIA GENERALE
English
Con Impact Factor ISI
Membrane Glycoproteins; Cell Nucleus; Cells, Cultured; Mycobacterium smegmatis; Cloning, Molecular; Cell Death; Receptors, Cell Surface; Humans; Flow Cytometry; Tumor Necrosis Factor-alpha; Interleukin-1; Mycobacterium bovis; Apoptosis; Annexin A5; Toll-Like Receptor 2; Signal Transduction; Recombinant Proteins; Macrophages; Toll-Like Receptors; Propidium; Gene Deletion; Bacterial Proteins; Mycobacterium tuberculosis; L-Lactate Dehydrogenase
Ciaramella, A., Cavone, A., Santucci, M.b., Garg, S., Sanarico, N., Bocchino, M., et al. (2004). Induction of apoptosis and release of interleukin-1 beta by cell wall-associated 19-kDa lipoprotein during the course of mycobacterial infection. THE JOURNAL OF INFECTIOUS DISEASES, 190(6), 1167-1176 [10.1086/423850].
Ciaramella, A; Cavone, A; Santucci, Mb; Garg, S; Sanarico, N; Bocchino, M; Galati, D; Martino, A; Auricchio, G; D'Orazio, M; Stewart, G; Neyrolles, O;...espandi
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2108/15445
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