Evidence map›Paper›PMID 33124769›Full record

ArticleEMBO reports2020

Irgm2 and Gate-16 cooperatively dampen Gram-negative bacteria-induced caspase-11 response.

Elif Eren, Rémi Planès, Salimata Bagayoko, Pierre-Jean Bordignon, Karima Chaoui, Audrey Hessel, Karin Santoni, Miriam Pinilla, Brice Lagrange, Odile Burlet-Schiltz and 4 more

Open access · bronzeAbstract read
In one paragraph

Article in EMBO reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
3.8field-weighted citation impact, top 5% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

43 citing papers in PubMed, 60 citations in OpenAlex.

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  13. The Interplay Between Autophagy and Regulated Necrosis.Antioxidants & redox signaling · 2023
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

14 authors at 4 institutions in 3 countries.

Elif Eren *Institute of Pharmacology and Structural Biology (IPBS), CNRS, UMR5089, University of Toulouse, Toulouse, France.ORCID 0000-0002-0328-5609
Rémi Planès *Institute of Pharmacology and Structural Biology (IPBS), CNRS, UMR5089, University of Toulouse, Toulouse, France.
Salimata BagayokoInstitute of Pharmacology and Structural Biology (IPBS), CNRS, UMR5089, University of Toulouse, Toulouse, France.ORCID 0000-0002-0956-4641
Pierre-Jean BordignonInstitute of Pharmacology and Structural Biology (IPBS), CNRS, UMR5089, University of Toulouse, Toulouse, France.
Karima ChaouiInstitute of Pharmacology and Structural Biology (IPBS), CNRS, UMR5089, University of Toulouse, Toulouse, France.
Audrey HesselInstitute of Pharmacology and Structural Biology (IPBS), CNRS, UMR5089, University of Toulouse, Toulouse, France.
Karin SantoniInstitute of Pharmacology and Structural Biology (IPBS), CNRS, UMR5089, University of Toulouse, Toulouse, France.
Miriam PinillaInstitute of Pharmacology and Structural Biology (IPBS), CNRS, UMR5089, University of Toulouse, Toulouse, France.
Brice LagrangeCIRI, Centre International de Recherche en Infectiologie, Inserm, U1111, CNRS, UMR5308, École Normale Supérieure de Lyon, Université Claude Bernard Lyon 1, Univ Lyon, Lyon, France.
Odile Burlet-SchiltzInstitute of Pharmacology and Structural Biology (IPBS), CNRS, UMR5089, University of Toulouse, Toulouse, France.
Jonathan C HowardFundação Calouste Gulbenkian, Instituto Gulbenkian de Ciência, Oeiras, Portugal.
Thomas HenryCIRI, Centre International de Recherche en Infectiologie, Inserm, U1111, CNRS, UMR5308, École Normale Supérieure de Lyon, Université Claude Bernard Lyon 1, Univ Lyon, Lyon, France.ORCID 0000-0002-0687-8565
Masahiro YamamotoDepartment of Immunoparasitology, Research Institute for Microbial Diseases, Osaka University, Osaka, Japan.
Etienne MeunierInstitute of Pharmacology and Structural Biology (IPBS), CNRS, UMR5089, University of Toulouse, Toulouse, France.ORCID 0000-0002-3651-4877
Centre National de la Recherche Scientifique · FRUniversité Claude Bernard Lyon 1 · FRCalouste Gulbenkian Foundation · PTThe University of Osaka · JP

Funding

IMMUNE NETWORK MODELS OF AUTO-IMMUNE DISEASESF05TW004809 · FIC · SANTA FE INSTITUTE · PI NEUMANN, AVIDAN U · 1992 to 1993
–
ATIP-AvenirEC | H2020 | H2020 Priority Excellent Science | H2020 European Research Council (ERC) INFLAME 804249European Society of Clinical Microbiology and Infectious Diseases (ESCMID)Fondation pour la Recherche Médicale (FRM) AJE20151034460Grant-in-Aid for Scientific Research 18H02642Grant-in-Aid for Scientific Research 18KK0226Grant-in-Aid for Scientific Research on Innovative Areas 19H04809Japanese Initiative for Progress of Research on Infectious Diseases for Global Epidemic JP19fm0208018MEXT | JST | Strategic International Collaborative Research Program (SICORP) 19jm0210067hMinistry of Education, Culture, Sports, Science and Technology of Japan 19H00970Research ProGram on Emerging and Re-emerging Infectious Diseases JP19fk0108047
6 · The paper itself

Abstract

Inflammatory caspase-11 (rodent) and caspases-4/5 (humans) detect the Gram-negative bacterial component LPS within the host cell cytosol, promoting activation of the non-canonical inflammasome. Although non-canonical inflammasome-induced pyroptosis and IL-1-related cytokine release are crucial to mount an efficient immune response against various bacteria, their unrestrained activation drives sepsis. This suggests that cellular components tightly control the threshold level of the non-canonical inflammasome in order to ensure efficient but non-deleterious inflammatory responses. Here, we show that the IFN-inducible protein Irgm2 and the ATG8 family member Gate-16 cooperatively counteract Gram-negative bacteria-induced non-canonical inflammasome activation, both in cultured macrophages and in vivo. Specifically, the Irgm2/Gate-16 axis dampens caspase-11 targeting to intracellular bacteria, which lowers caspase-11-mediated pyroptosis and cytokine release. Deficiency in Irgm2 or Gate16 induces both guanylate binding protein (GBP)-dependent and GBP-independent routes for caspase-11 targeting to intracellular bacteria. Our findings identify molecular effectors that fine-tune bacteria-activated non-canonical inflammasome responses and shed light on the understanding of the immune pathways they control.

Indexed as

CaspasesLipopolysaccharidesAutophagy-Related Protein 8 FamilyCaspases, InitiatorGram-Negative BacteriaInflammasomesMacrophagesAutophagy-Related Protein 8 FamilyCaspasesCaspases, InitiatorGABARAPL2 protein, humanInflammasomesLipopolysaccharidesCaspase-11Gate-16infections/InterferonsIrgm2non-canonical inflammasome

Identifiers

PMID33124769
PMCPMC7645206
OpenAlexW3097072608

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.