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Dorhoi, A.* ; Nouailles, G.* ; Jörg, S.* ; Hagens, K.* ; Heinemann, E.* ; Pradl, L.* ; Oberbeck-Müller, D.* ; Duque-Correa, M.A.* ; Reece, S.T.* ; Ruland, J. ; Brosch, R.* ; Tschopp, J.* ; Gross, O.* ; Kaufmann, S.H.*

Activation of the NLRP3 inflammasome by Mycobacterium tuberculosis is uncoupled from susceptibility to active tuberculosis.

Eur. J. Immunol. 42, 374-384 (2012)
Verlagsversion Volltext DOI
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Open Access Green möglich sobald Postprint bei der ZB eingereicht worden ist.
As a hallmark of tuberculosis (TB), Mycobacterium tuberculosis (MTB) induces granulomatous lung lesions and systemic inflammatory responses during active disease. Molecular regulation of inflammation is associated with inflammasome assembly. We determined the extent to which MTB triggers inflammasome activation and how this impacts on the severity of TB in a mouse model. MTB stimulated release of mature IL-1β in macrophages while attenuated M. bovis BCG failed to do so. Tubercle bacilli specifically activated the NLRP3 inflammasome and this propensity was strictly controlled by the virulence-associated RD1 locus of MTB. However, Nlrp3-deficient mice controlled pulmonary TB, a feature correlated with NLRP3-independent production of IL-1β in infected lungs. Our studies demonstrate that MTB activates the NLRP3 inflammasome in macrophages in an ESX-1-dependent manner. However, during TB, MTB promotes NLRP3- and caspase-1-independent IL-1β release in myeloid cells recruited to lung parenchyma and thus overcomes NLRP3 deficiency in vivo in experimental models.
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Publikationstyp Artikel: Journalartikel
Dokumenttyp Wissenschaftlicher Artikel
Schlagwörter ESX-1 secretion system; Inflammasome; IL-1β; Mycobacterium tuberculosis; NLRP3
ISSN (print) / ISBN 0014-2980
e-ISSN 1521-4141
Quellenangaben Band: 42, Heft: 2, Seiten: 374-384 Artikelnummer: , Supplement: ,
Verlag Wiley
Verlagsort Hoboken
Begutachtungsstatus Peer reviewed