Evidence map›Paper›PMID 38180443›Full record

ArticleThe Journal of experimental medicine2024

Notch2 with retinoic acid license IL-23 expression by intestinal EpCAM+ DCIR2+ cDC2s in mice.

Daiya Ohara, Yusuke Takeuchi, Hitomi Watanabe, Yoonha Lee, Hiroki Mukoyama, Toshiaki Ohteki, Gen Kondoh, Keiji Hirota

Open access · hybridAbstract read
In one paragraph

Article in The Journal of experimental medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
2.4field-weighted citation impact, top 12% 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

6 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Review
  6. IL-23 to see: Gut DCs shine bright in inductive sites.The Journal of experimental medicine · 2024
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 2 institutions in 1 country.

Daiya OharaLaboratory of Integrative Biological Science, Institute for Life and Medical Sciences, Kyoto University , Kyoto, Japan.ORCID 0009-0004-7946-6352
Yusuke TakeuchiLaboratory of Integrative Biological Science, Institute for Life and Medical Sciences, Kyoto University , Kyoto, Japan.ORCID 0000-0003-2491-9524
Hitomi WatanabeLaboratory of Integrative Biological Science, Institute for Life and Medical Sciences, Kyoto University , Kyoto, Japan.ORCID 0000-0001-6448-9966
Yoonha LeeLaboratory of Integrative Biological Science, Institute for Life and Medical Sciences, Kyoto University , Kyoto, Japan.ORCID 0009-0009-8098-9966
Hiroki MukoyamaLaboratory of Integrative Biological Science, Institute for Life and Medical Sciences, Kyoto University , Kyoto, Japan.ORCID 0000-0001-6871-5182
Toshiaki OhtekiDepartment of Biodefense Research, Medical Research Institute, Tokyo Medical and Dental University, Tokyo, Japan.ORCID 0000-0002-8088-5165
Gen KondohLaboratory of Integrative Biological Science, Institute for Life and Medical Sciences, Kyoto University , Kyoto, Japan.ORCID 0000-0002-2564-0149
Keiji HirotaLaboratory of Integrative Biological Science, Institute for Life and Medical Sciences, Kyoto University , Kyoto, Japan.ORCID 0000-0002-4737-0661
Kyoto University · JPTokyo Medical and Dental University · JP

Funding

Japan Society for the Promotion of Science 22J20213Naito FoundationShimizu Foundation for Immunology and Neuroscience
6 · The paper itself

Abstract

Despite the importance of IL-23 in mucosal host defense and disease pathogenesis, the mechanisms regulating the development of IL-23-producing mononuclear phagocytes remain poorly understood. Here, we employed an Il23aVenus reporter strain to investigate the developmental identity and functional regulation of IL-23-producing cells. We showed that flagellin stimulation or Citrobacter rodentium infection led to robust induction of IL-23-producing EpCAM+ DCIR2+ CD103- cDC2s, termed cDCIL23, which was confined to gut-associated lymphoid tissues, including the mesenteric lymph nodes, cryptopatches, and isolated lymphoid follicles. Furthermore, we demonstrated that Notch2 signaling was crucial for the development of EpCAM+ DCIR2+ cDC2s, and the combination of Notch2 signaling with retinoic acid signaling controlled their terminal differentiation into cDCIL23, supporting a two-step model for the development of gut cDCIL23. Our findings provide fundamental insights into the developmental pathways and cellular dynamics of IL-23-producing cDC2s at steady state and during pathogen infection.

Indexed as

Dendritic CellsEnterobacteriaceae InfectionsInterleukin-23AnimalsEpithelial Cell Adhesion MoleculeFlagellinMiceTretinoinEpithelial Cell Adhesion MoleculeFlagellinInterleukin-23Tretinoin

Identifiers

PMID38180443
PMCPMC10770806
OpenAlexW4390631551

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.