Apoptosis of macrophages during pulmonary Mycobacterium bovis infection: correlation with intracellular bacillary load and cytokine levels


Autoria(s): RODRIGUES, Michele F.; BARSANTE, Michele M.; ALVES, Caio C. S.; SOUZA, Maria A.; FERREIRA, Ana P.; AMARANTE-MENDES, Gustavo P.; TEIXEIRA, Henrique C.
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

20/10/2012

20/10/2012

2009

Resumo

P>Apoptosis of macrophages infected with pathogenic mycobacteria is an alternative host defence capable of removing the environment supporting bacterial growth. In this work the influence of virulence and bacterial load on apoptosis of alveolar macrophages during the initial phase of infection by Mycobacterium bovis was investigated. BALB/c mice were infected intratracheally with high or low doses of the virulent (ATCC19274) or attenuated (bacillus Calmette-Guerin Moreau) strains of M. bovis. The frequency of macrophage apoptosis, the growth of mycobacteria in macrophages, and the in situ levels of the cytokines tumour necrosis factor-alpha (TNF-alpha), interleukin-10 (IL-10) and IL-12 and of the anti-apoptotic protein Bcl-2 were measured at day 3 and day 7 post-infection. An increase of macrophage apoptosis was observed after infection with both strains but the virulent strain induced less apoptosis than the attenuated strain. On the 3rd day after infection with the virulent strain macrophage apoptosis was reduced in the high-dose group, while on the 7th day post-infection macrophage apoptosis was reduced in the low-dose group. Inhibition of apoptosis was correlated with increased production of IL-10, reduced production of TNF-alpha and increased production of Bcl-2. In addition, the production of IL-12 was reduced at points where the lowest levels of macrophage apoptosis were observed. Our results indicate that virulent mycobacteria are able to modulate macrophage apoptosis to an extent dependent on the intracellular bacterial burden, which benefits its intracellular growth and dissemination to adjacent cells.

Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)

CNPq[479724/2007-5]

CNPq[310912/2006-7]

Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)

FAPEMIG[CBB PPM 0247/08]

Fundação de Amparo à Pesquisa do Estado de Minas Gerais (FAPEMIG)

Identificador

IMMUNOLOGY, v.128, n.1, p.e691-e699, 2009

0019-2805

http://producao.usp.br/handle/BDPI/28293

10.1111/j.1365-2567.2009.03062.x

http://dx.doi.org/10.1111/j.1365-2567.2009.03062.x

Idioma(s)

eng

Publicador

WILEY-BLACKWELL PUBLISHING, INC

Relação

Immunology

Direitos

restrictedAccess

Copyright WILEY-BLACKWELL PUBLISHING, INC

Palavras-Chave #apoptosis #cytokines #infection #macrophages #mycobacteria #CASPASE-INDEPENDENT PATHWAY #TUMOR-NECROSIS-FACTOR #TUBERCULOSIS INFECTION #TNF-ALPHA #ALVEOLAR MACROPHAGES #IMMUNE-RESPONSES #HOST MACROPHAGES #DENDRITIC CELLS #CALMETTE-GUERIN #UP-REGULATION #Immunology
Tipo

article

original article

publishedVersion