Publication | Open Access
Induction of Apoptosis and Release of Interleukin‐1β by Cell Wall–Associated 19‐kDa Lipoprotein during the Course of Mycobacterial Infection
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Citations
40
References
2004
Year
Microbial PathogensImmunologyCell DeathPathologyBacterial PathogensInflammationHost ResponseMedical MicrobiologyM. TuberculosisInfection ControlImmunopathologyPulmonary TuberculosisBacterial InfectionsTuberculosis19-Kda Lipoprotein KoClinical MicrobiologyPhagocyteCytokinePathogenesis19-Kda Lipoprotein SignalingMicrobiologyMycobacterial InfectionMedicine
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.
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