Bim is a crucial regulator of apoptosis induced by Mycobacterium tuberculosis

Aguiló, N. (Universidad de Zaragoza) ; Uranga, S. (Universidad de Zaragoza) ; Marinova, D. (Universidad de Zaragoza) ; Martín, C. (Universidad de Zaragoza) ; Pardo, J. (Universidad de Zaragoza)

Resumen: Mycobacterium tuberculosis, the causative agent of tuberculosis, induces apoptosis in infected macrophages in vitro and in vivo. However, the molecular mechanism controlling this process is not known. In order to study the involvement of the mitochondrial apoptotic pathway in M. tuberculosis-induced apoptosis, we analysed cell death in M. tuberculosis-infected embryonic fibroblasts (MEFs) derived from different knockout mice for genes involved in this route. We found that apoptosis induced by M. tuberculosis is abrogated in the absence of Bak and Bax, caspase 9 or the executioner caspases 3 and 7. Notably, we show that MEF deficient in the BH3-only BCL-2-interacting mediator of cell death (Bim) protein were also resistant to this process. The relevance of these results has been confirmed in the mouse macrophage cell line J774, where cell transfection with siRNA targeting Bim impaired apoptosis induced by virulent mycobacteria. Notably, only infection with a virulent strain, but not with attenuated ESX-1-defective strains, such as Bacillus Calmette-Guerin and live-attenuated M. tuberculosis vaccine strain MTBVAC, induced Bim upregulation and apoptosis, probably implicating virulence factor early secreted antigenic target 6-kDa protein in this process. Our results suggest that Bim upregulation and apoptosis is mediated by the p38MAPK-dependent pathway. Our findings show that Bim is a master regulator of apoptosis induced by M. tuberculosis.

Idioma: Inglés

DOI: 10.1038/cddis.2014.313

Año: 2014

Publicado en: CELL DEATH & DISEASE 5, 7 (2014), e1343 [10 pp.]
ISSN: 2041-4889

Factor impacto JCR: 5.014 (2014)

Categ. JCR: CELL BIOLOGY rank: 49 / 184 = 0.266 (2014) - Q2 - T1

Tipo y forma: Artículo (Versión definitiva)

Área (Departamento): Área Microbiología (Dpto. Microb.Med.Pr.,Sal.Públ.)
Área (Departamento): Área Inmunología (Dpto. Microb.Med.Pr.,Sal.Públ.)
Área (Departamento): Proy. investigación HQA (Dpto. Microb.Med.Pr.,Sal.Públ.)