Evidence map›Paper›PMID 26355151›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2015

Multi-Inhibitory Effects of A2A Adenosine Receptor Signaling on Neutrophil Adhesion Under Flow.

Tadayuki Yago, Hiroki Tsukamoto, Zhenghui Liu, Ying Wang, Linda F Thompson, Rodger P McEver

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
3.4field-weighted citation impact, top 9% 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

28 citing papers in PubMed, 42 citations in OpenAlex.

  1. Review
  2. Review
  3. APurinergic signalling · 2022
    Article
  4. Article
  5. Secondary Burn Progression Mitigated by an Adenosine 2A Receptor Agonist.Journal of burn care & research : official publication of the American Burn Association · 2022
    Article
  6. Anti-Inflammatory Metabolites in the Pathogenesis of Bacterial Infection.Frontiers in cellular and infection microbiology · 2022
    Review
  7. Review
  8. Adenosine and Inflammation: Here, There and Everywhere.International journal of molecular sciences · 2021
    Review
  9. Review
  10. Review
  11. Targeting Immunometabolism in Glioblastoma.Frontiers in oncology · 2021
    Review
  12. The adenosine pathway in immuno-oncology.Nature reviews. Clinical oncology · 2020
    Review
  13. Article
  14. Review
  15. Article
  16. Anti-Inflammatory Profile ofMediators of inflammation · 2020
    Article
  17. Adenosine and the Cardiovascular System.American journal of cardiovascular drugs : drugs, devices, and other interventions · 2019
    Review
  18. Article
  19. Article
  20. 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

6 authors at 3 institutions in 2 countries.

Tadayuki YagoCardiovascular Biology Program, Oklahoma Medical Research Foundation, Oklahoma City, OK 73104;
Hiroki TsukamotoImmunobiology and Cancer Program, Oklahoma Medical Research Foundation, Oklahoma City, OK 73104; Laboratory of Oncology, Pharmacy Practice and Sciences, Graduate School of Pharmaceutical Sciences, Tohoku University, Sendai 980-8578, Japan;
Zhenghui LiuCardiovascular Biology Program, Oklahoma Medical Research Foundation, Oklahoma City, OK 73104;
Ying WangCardiovascular Biology Program, Oklahoma Medical Research Foundation, Oklahoma City, OK 73104; Department of Biochemistry and Molecular Biology, University of Oklahoma Health Sciences Center, Oklahoma City, OK 73104; and.
Linda F ThompsonImmunobiology and Cancer Program, Oklahoma Medical Research Foundation, Oklahoma City, OK 73104; Department of Microbiology and Immunology, University of Oklahoma Health Sciences Center, Oklahoma City, OK 73104 linda-thompson@omrf.org rodger-mcever@omrf.org.
Rodger P McEverCardiovascular Biology Program, Oklahoma Medical Research Foundation, Oklahoma City, OK 73104; Department of Biochemistry and Molecular Biology, University of Oklahoma Health Sciences Center, Oklahoma City, OK 73104; and linda-thompson@omrf.org rodger-mcever@omrf.org.
Oklahoma Medical Research Foundation · USTohoku Medical and Pharmaceutical University · JPUniversity of Oklahoma Health Sciences Center · US

Funding

Signal-dependent neutrophil adhesion to vascular surfacesR01HL034363 · NHLBI · UNIVERSITY OF TEXAS HLTH SCI CTR SAN ANT · PI MCEVER, RODGER PAUL · 1985 to 2017
$3.9M
CYTOPLASMIC REGULATION OF P-SELECTIN/PSGL-1 INTERACTIONSR37HL034363 · NHLBI · UNIVERSITY OF OKLAHOMA HLTH SCIENCES CTR · PI MCEVER, RODGER PAUL · 1998 to 2007
$3.3M
The Regulation of Inflammatory Responses by CD73R01AI018220 · NIAID · SCRIPPS CLINIC AND RESEARCH FOUNDATION · PI THOMPSON, LINDA F · 1985 to 2012
$3.1M
NHLBI NIH HHS HL034363NHLBI NIH HHS R01 HL034363NHLBI NIH HHS R37 HL034363NIAID NIH HHS AI18220NIAID NIH HHS R01 AI018220
6 · The paper itself

Abstract

A2A adenosine receptor (A2AAR) signaling negatively regulates inflammatory responses in many disease models, but the detailed mechanisms remain unclear. We used the selective A2AAR agonist, ATL313, to examine how A2AAR signaling affects human and murine neutrophil adhesion under flow. Treating neutrophils with ATL313 inhibited selectin-induced, β2 integrin-dependent slow rolling and chemokine-induced, β2 integrin-dependent arrest on ICAM-1. ATL313 inhibited selectin-induced β2 integrin extension, which supports slow rolling, and chemokine-induced hybrid domain "swing-out," which supports arrest. Furthermore, ATL313 inhibited integrin outside-in signaling as revealed by reduced neutrophil superoxide production and spreading on immobilized anti-β2 integrin Ab. ATL313 suppressed selectin-triggered activation of Src family kinases (SFKs) and p38 MAPK, chemokine-triggered activation of Ras-related protein 1, and β2 integrin-triggered activation of SFKs and Vav cytoskeletal regulatory proteins. ATL313 activated protein kinase A and its substrate C-terminal Src kinase, an inhibitor of SFKs. Treating neutrophils with a protein kinase A inhibitor blocked the actions of ATL313. In vivo, ATL313-treated neutrophils rolled faster and arrested much less frequently in postcapillary venules of the murine cremaster muscle after TNF-α challenge. Furthermore, ATL313 markedly suppressed neutrophil migration into the peritoneum challenged with thioglycollate. ATL313 did not affect A2AAR-deficient neutrophils, confirming its specificity. Our findings provide new insights into the anti-inflammatory mechanisms of A2AAR signaling and the potential utility of A2AAR agonists in inflammatory diseases.

Indexed as

AnimalsCD18 AntigensCell AdhesionHumansLeukocyte RollingMiceMice, KnockoutNeutrophilsPiperidinesProto-Oncogene Proteins c-vavReceptor, Adenosine A2ASignal Transductionsrc-Family KinasesTumor Necrosis Factor-alphaATL 313CD18 AntigensPiperidinesProto-Oncogene Proteins c-vavReceptor, Adenosine A2Asrc-Family KinasesTumor Necrosis Factor-alpha

Identifiers

PMID26355151
PMCPMC4592819
OpenAlexW1848588865

What OpenQuestion holds

Textmetadata
LicenceTDM
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.