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(Reference retrieved automatically from Web of Science through information on FAPESP grant and its corresponding number as mentioned in the publication by the authors.)

Leishmania Lipophosphoglycan Triggers Caspase-11 and the Non-canonical Activation of the NLRP3 Inflammasome

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Author(s):
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de Carvalho, Renan V. H. [1] ; Andrade, Warrison A. [1] ; Lima-Junior, Djalma S. [1] ; Dilucca, Marisa [1] ; de Oliveira, V, Caroline ; Wang, Kun [2] ; Nogueira, Paula M. [3] ; Rugani, Jeronimo N. [3] ; Soares, Rodrigo P. [3] ; Beverley, Stephen M. [4] ; Shao, Feng [2] ; Zamboni, Dario S. [5]
Total Authors: 12
Affiliation:
[1] Univ Sao Paulo, Fac Med Ribeirao Preto, Dept Biol Celular & Mol & Bioagentes Patogen, Ribeirao Preto, SP - Brazil
[2] Natl Inst Biol Sci, Beijing 102206 - Peoples R China
[3] Fundacao Oswaldo Cruz FIOCRUZ, Inst Rene Rachou, Belo Horizonte, MG - Brazil
[4] Washington Univ, Sch Med, Dept Mol Microbiol, St Louis, MO 63110 - USA
[5] de Oliveira, Caroline, V, Univ Sao Paulo, Fac Med Ribeirao Preto, Dept Biol Celular & Mol & Bioagentes Patogen, Ribeirao Preto, SP - Brazil
Total Affiliations: 5
Document type: Journal article
Source: CELL REPORTS; v. 26, n. 2, p. 429+, JAN 8 2019.
Web of Science Citations: 12
Abstract

Activation of the NLRP3 inflammasome by Leishmania parasites is critical for the outcome of leishmaniasis, a disease that affects millions of people worldwide. We investigate the mechanisms involved in NLRP3 activation and demonstrate that caspase-11 (CASP11) is activated in response to infection by Leishmania species and triggers the non-canonical activation of NLRP3. This process accounts for host resistance to infection in macrophages and in vivo. We identify the parasite membrane glycoconjugate lipophosphoglycan (LPG) as the molecule involved in CASP11 activation. Cytosolic delivery of LPG in macrophages triggers CASP11 activation, and infections performed with Lpg1(-/-) parasites reduce CASP11/NLRP3 activation. Unlike bacterial LPS, purified LPG does not activate mouse CASP11 (or human Casp4) in vitro, suggesting the participation of additional molecules for LPG-mediated CASP11 activation. Our data identify a parasite molecule involved in CASP11 activation, thereby establishing the mechanisms underlying inflammasome activation in response to Leishmania species. (AU)

FAPESP's process: 13/08216-2 - CRID - Center for Research in Inflammatory Diseases
Grantee:Fernando de Queiroz Cunha
Support Opportunities: Research Grants - Research, Innovation and Dissemination Centers - RIDC
FAPESP's process: 14/04684-4 - The inflammasome in the host response against intracellular pathogens and the microbial mechanisms for its evasion
Grantee:Dario Simões Zamboni
Support Opportunities: Research Projects - Thematic Grants