Evidence map›Paper›PMID 34548395›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2021

The ATP-hydrolyzing ectoenzyme E-NTPD8 attenuates colitis through modulation of P2X4 receptor-dependent metabolism in myeloid cells.

Haruka Tani, Bo Li, Takashi Kusu, Ryu Okumura, Junichi Nishimura, Daisuke Okuzaki, Daisuke Motooka, Shoya Arakawa, Asuka Mori, Terukazu Yoshihara and 10 more

Open access · hybridAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed, 28 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Review
  5. Article
  6. Article
  7. Targeting P2X Receptors-Current Progress in Sepsis.International journal of inflammation · 2025
    Review
  8. Article
  9. Review
  10. Ion channel regulation of gut immunity.The Journal of general physiology · 2023
    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

20 authors at 4 institutions in 1 country.

Haruka TaniDepartment of Microbiology and Immunology, Graduate School of Medicine, Osaka University, Osaka 565-0871, Japan.
Bo LiDepartment of Microbiology and Immunology, Graduate School of Medicine, Osaka University, Osaka 565-0871, Japan.
Takashi KusuDepartment of Microbiology and Immunology, Graduate School of Medicine, Osaka University, Osaka 565-0871, Japan.
Ryu OkumuraDepartment of Microbiology and Immunology, Graduate School of Medicine, Osaka University, Osaka 565-0871, Japan.ORCID 0000-0001-9569-4591
Junichi NishimuraDepartment of Microbiology and Immunology, Graduate School of Medicine, Osaka University, Osaka 565-0871, Japan.
Daisuke OkuzakiThe World Premier International Research Center Initiative (WPI) Immunology Frontier Research Center, Osaka University, Osaka 565-0871, Japan.ORCID 0000-0002-4552-783X
Daisuke MotookaIntegrated Frontier Research for Medical Science Division, Institute for Open and Transdisciplinary Research Initiatives, Osaka University, Osaka 565-0871, Japan.
Shoya ArakawaDepartment of Biotechnology, Graduate School of Engineering, Osaka University, Osaka 565-0871, Japan.
Asuka MoriDepartment of Biotechnology, Graduate School of Engineering, Osaka University, Osaka 565-0871, Japan.
Terukazu YoshiharaDepartment of Gastroenterological Surgery, Graduate School of Medicine, Osaka University, Osaka 565-0871, Japan.
Takayuki OginoDepartment of Gastroenterological Surgery, Graduate School of Medicine, Osaka University, Osaka 565-0871, Japan.
Shih-Han TsaiDepartment of Microbiology and Immunology, Graduate School of Medicine, Osaka University, Osaka 565-0871, Japan.
Yoki FurutaDepartment of Microbiology and Immunology, Graduate School of Medicine, Osaka University, Osaka 565-0871, Japan.
Masato MunetaDepartment of Microbiology and Immunology, Graduate School of Medicine, Osaka University, Osaka 565-0871, Japan.
Shota NakamuraIntegrated Frontier Research for Medical Science Division, Institute for Open and Transdisciplinary Research Initiatives, Osaka University, Osaka 565-0871, Japan.
Eiichiro FukusakiDepartment of Biotechnology, Graduate School of Engineering, Osaka University, Osaka 565-0871, Japan.
Kimiko YamamotoLaboratory of System Physiology, Department of Biomedical Engineering, Graduate School of Medicine, University of Tokyo, Tokyo 113-0033, Japan.ORCID 0000-0002-0700-4149
Hideo YagitaDepartment of Immunology, Juntendo University School of Medicine, Tokyo 113-8421, Japan.
Hisako KayamaDepartment of Microbiology and Immunology, Graduate School of Medicine, Osaka University, Osaka 565-0871, Japan; kayama@ongene.med.osaka-u.ac.jp ktakeda@ongene.med.osaka-u.ac.jp.ORCID 0000-0001-5676-8228
Kiyoshi TakedaDepartment of Microbiology and Immunology, Graduate School of Medicine, Osaka University, Osaka 565-0871, Japan; kayama@ongene.med.osaka-u.ac.jp ktakeda@ongene.med.osaka-u.ac.jp.
The University of Osaka · JPOsaka International University · JPJuntendo University · JPThe University of Tokyo · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Extracellular adenosine triphosphate (ATP) released by mucosal immune cells and by microbiota in the intestinal lumen elicits diverse immune responses that mediate the intestinal homeostasis via P2 purinergic receptors, while overactivation of ATP signaling leads to mucosal immune system disruption, which leads to pathogenesis of intestinal inflammation. In the small intestine, hydrolysis of luminal ATP by ectonucleoside triphosphate diphosphohydrolase (E-NTPD)7 in epithelial cells is essential for control of the number of T helper 17 (Th17) cells. However, the molecular mechanism by which microbiota-derived ATP in the colon is regulated remains poorly understood. Here, we show that E-NTPD8 is highly expressed in large-intestinal epithelial cells and hydrolyzes microbiota-derived luminal ATP. Compared with wild-type mice,

Indexed as

GlycolysisAdenosine TriphosphatasesAdenosine TriphosphateAnimalsCells, CulturedColitisFemaleMiceMice, Inbred C57BLMice, KnockoutMyeloid CellsReceptors, Purinergic P2X4Signal TransductionTh17 CellsAdenosine TriphosphatasesAdenosine Triphosphatenucleoside triphosphate diphosphohydrolase 8, mouseReceptors, Purinergic P2X4adenosine triphosphatecolitisE-NTPD8immunometabolismP2X4R

Identifiers

PMID34548395
PMCPMC8488689
OpenAlexW3200573297

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.