Evidence map›Paper›PMID 36941399›Full record

ArticleNature immunology2023

Epithelial Nlrp10 inflammasome mediates protection against intestinal autoinflammation.

Danping Zheng, Gayatree Mohapatra, Lara Kern, Yiming He, Merav D Shmueli, Rafael Valdés-Mas, Aleksandra A Kolodziejczyk, Tomasz Próchnicki, Matilde B Vasconcelos, Lena Schorr and 20 more

Abstract read
PubMed Publisher
In one paragraph

Article in Nature immunology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
5.1field-weighted citation impact, top 4% 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

24 citing papers in PubMed, 34 citations in OpenAlex.

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  9. The gut microbiome connects nutrition and human health.Nature reviews. Gastroenterology & hepatology · 2025
    Review
  10. Review
  11. Review
  12. Pattern Recognition by NOD-Like Receptors.Advances in experimental medicine and biology · 2025
    Review
  13. IL-18 and IL-18BP: A Unique Dyad in Health and Disease.International journal of molecular sciences · 2024
    Review
  14. Article
  15. Article
  16. Review
  17. NLRP inflammasomes in health and disease.Molecular biomedicine · 2024
    Review
  18. Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

30 authors at 6 institutions in 5 countries.

Danping Zheng *Systems Immunology Department, Weizmann Institute of Science, Rehovot, Israel.
Gayatree Mohapatra *Systems Immunology Department, Weizmann Institute of Science, Rehovot, Israel.
Lara Kern *Systems Immunology Department, Weizmann Institute of Science, Rehovot, Israel.ORCID 0000-0001-8399-6293
Yiming HeSystems Immunology Department, Weizmann Institute of Science, Rehovot, Israel.
Merav D ShmueliSystems Immunology Department, Weizmann Institute of Science, Rehovot, Israel.ORCID 0000-0002-9196-7633
Rafael Valdés-MasSystems Immunology Department, Weizmann Institute of Science, Rehovot, Israel.
Aleksandra A KolodziejczykSystems Immunology Department, Weizmann Institute of Science, Rehovot, Israel.ORCID 0000-0002-2903-8884
Tomasz PróchnickiInstitute of Innate Immunity, Medical Faculty, University of Bonn, Bonn, Germany.
Matilde B VasconcelosInstitute of Innate Immunity, Medical Faculty, University of Bonn, Bonn, Germany.ORCID 0000-0003-1487-6495
Lena SchorrDivision of Cancer-Microbiome Research, German Cancer Research Center, Heidelberg, Germany.ORCID 0000-0002-3781-5663
Franziska HertelDivision of Cancer-Microbiome Research, German Cancer Research Center, Heidelberg, Germany.ORCID 0000-0003-1347-5753
Ye Seul LeeDivision of Cancer-Microbiome Research, German Cancer Research Center, Heidelberg, Germany.
Miguel Camacho RufinoSystems Immunology Department, Weizmann Institute of Science, Rehovot, Israel.
Emmanuelle CeddahaSystems Immunology Department, Weizmann Institute of Science, Rehovot, Israel.
Sandy ShimshySystems Immunology Department, Weizmann Institute of Science, Rehovot, Israel.
Ryan James HodgettsSystems Immunology Department, Weizmann Institute of Science, Rehovot, Israel.
Mally Dori-BachashSystems Immunology Department, Weizmann Institute of Science, Rehovot, Israel.
Christian KleimeyerSystems Immunology Department, Weizmann Institute of Science, Rehovot, Israel.
Kim GoldenbergSystems Immunology Department, Weizmann Institute of Science, Rehovot, Israel.
Melina HeinemannSystems Immunology Department, Weizmann Institute of Science, Rehovot, Israel.
Noa StettnerDepartment of Veterinary Resources, Weizmann Institute of Science, Rehovot, Israel.
Alon HarmelinDepartment of Veterinary Resources, Weizmann Institute of Science, Rehovot, Israel.
Hagit ShapiroSystems Immunology Department, Weizmann Institute of Science, Rehovot, Israel.
Jens PuschhofDivision of Cancer-Microbiome Research, German Cancer Research Center, Heidelberg, Germany.
Minhu ChenDepartment of Gastroenterology, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
Richard A FlavellDepartment of Immunobiology, Yale University School of Medicine, New Haven, CT, USA.ORCID 0000-0003-4461-0778
Eicke LatzInstitute of Innate Immunity, Medical Faculty, University of Bonn, Bonn, Germany.ORCID 0000-0003-1488-5666
Yifat MerblSystems Immunology Department, Weizmann Institute of Science, Rehovot, Israel.ORCID 0000-0002-3465-2221
Suhaib K AbdeenSystems Immunology Department, Weizmann Institute of Science, Rehovot, Israel. suhib.abdin@weizmann.ac.il.
Eran ElinavSystems Immunology Department, Weizmann Institute of Science, Rehovot, Israel. eran.elinav@weizmann.ac.il.ORCID 0000-0002-5775-2110
Weizmann Institute of Science · ILGerman Cancer Research Center · DESun Yat-sen University · CNUniversity of Bonn · DEHoward Hughes Medical Institute · USUniversity of Manchester · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Unlike other nucleotide oligomerization domain-like receptors, Nlrp10 lacks a canonical leucine-rich repeat domain, suggesting that it is incapable of signal sensing and inflammasome formation. Here we show that mouse Nlrp10 is expressed in distal colonic intestinal epithelial cells (IECs) and modulated by the intestinal microbiome. In vitro, Nlrp10 forms an Apoptosis-associated speck-like protein containing a caspase-recruitment domain (ASC)-dependent, m-3M3FBS-activated, polyinosinic:polycytidylic acid-modulated inflammasome driving interleukin-1β and interleukin-18 secretion. In vivo, Nlrp10 signaling is dispensable during steady state but becomes functional during autoinflammation in antagonizing mucosal damage. Importantly, whole-body or conditional IEC Nlrp10 depletion leads to reduced IEC caspase-1 activation, coupled with enhanced susceptibility to dextran sodium sulfate-induced colitis, mediated by altered inflammatory and healing programs. Collectively, understanding Nlrp10 inflammasome-dependent and independent activity, regulation and possible human relevance might facilitate the development of new innate immune anti-inflammatory interventions.

Indexed as

Apoptosis Regulatory ProteinsInflammasomesAdaptor Proteins, Signal TransducingAnimalsApoptosisCarrier ProteinsCaspase 1HumansInterleukin-1betaMiceNLR Family, Pyrin Domain-Containing 3 ProteinAdaptor Proteins, Signal TransducingApoptosis Regulatory ProteinsCarrier ProteinsCaspase 1InflammasomesInterleukin-1betaNLR Family, Pyrin Domain-Containing 3 ProteinNLRP10 protein, humanNLRP10 protein, mouse

Identifiers

PMID36941399
OpenAlexW4328048600

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.