Evidence map›Paper›PMID 33884657›Full record

ArticleJournal of leukocyte biology2022

CD200R1L is a functional evolutionary conserved activating receptor in human neutrophils.

M Inês Pascoal Ramos, Can Keşmir, Jorn E Stok, Ruben Geerdink, Nikolaos Satravelas, Geertje H A Westerlaken, Linde Meyaard, Michiel van der Vlist

Open access · hybridAbstract read
In one paragraph

Article in Journal of leukocyte biology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.6field-weighted citation impact, top 33% 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

5 citing papers in PubMed, 8 citations in OpenAlex.

  1. Trial
  2. Article
  3. Review
  4. Article
  5. 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 3 institutions in 1 country.

M Inês Pascoal RamosCenter for Translational Immunology, Dept. Immunology, University Medical Center Utrecht, Utrecht University, Oncode Institute, Utrecht, The Netherlands.
Can KeşmirTheoretical Biology and Bioinformatics, Department of Biology, Utrecht University, Utrecht, The Netherlands.
Jorn E StokCenter for Translational Immunology, Dept. Immunology, University Medical Center Utrecht, Utrecht University, Oncode Institute, Utrecht, The Netherlands.
Ruben GeerdinkCenter for Translational Immunology, Dept. Immunology, University Medical Center Utrecht, Utrecht University, Oncode Institute, Utrecht, The Netherlands.
Nikolaos SatravelasTheoretical Biology and Bioinformatics, Department of Biology, Utrecht University, Utrecht, The Netherlands.
Geertje H A WesterlakenCenter for Translational Immunology, Dept. Immunology, University Medical Center Utrecht, Utrecht University, Oncode Institute, Utrecht, The Netherlands.
Linde MeyaardCenter for Translational Immunology, Dept. Immunology, University Medical Center Utrecht, Utrecht University, Oncode Institute, Utrecht, The Netherlands.
Michiel van der VlistCenter for Translational Immunology, Dept. Immunology, University Medical Center Utrecht, Utrecht University, Oncode Institute, Utrecht, The Netherlands.
Utrecht University · NLUniversity Medical Center Utrecht · NLOncode Institute · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Inhibitory and activating immune receptors play a key role in modulating the amplitude and duration of immune responses during infection and in maintaining immune balance in homeostatic conditions. The CD200 Receptor (CD200R) gene family in humans encodes one inhibitory receptor, CD200R1, and one putative activating member, CD200R1 Like (CD200R1L). It is demonstrated that CD200R1L is endogenously expressed by human neutrophils and activates cellular functions such as reactive oxygen species (ROS) production via Syk, PI3Kβ, PI3Kδ, and Rac GTPase signaling. Phylogenetic analysis shows that CD200R1L is present in many species among vertebrates, ranging from birds to primates, suggesting that evolutionary conservation of this receptor is critical for protection against co-evolving pathogens. The duplication event that generated CD200R1L from CD200R occurred several times throughout evolution, supporting convergent evolution of CD200R1L. In our phylogenetic trees, CD200R1L has longer branch lengths than CD200R1 in most species, suggesting that CD200R1L is evolving faster than CD200R1. It is proposed that CD200R1L represents a hitherto uncharacterized activating receptor on human neutrophils.

Indexed as

Evolution, MolecularAntibodies, MonoclonalHumansInterleukin-8NeutrophilsOrexin ReceptorsPhosphatidylinositol 3-KinasesPhylogenyrac GTP-Binding ProteinsReactive Oxygen SpeciesSyk KinaseAntibodies, MonoclonalCD200R1 protein, humanCXCL8 protein, humanInterleukin-8Orexin ReceptorsPhosphatidylinositol 3-Kinasesrac GTP-Binding ProteinsReactive Oxygen SpeciesSyk KinaseSYK protein, humanNETosisphylogenyreactive oxygen species

Identifiers

PMID33884657
PMCPMC9291319
OpenAlexW3153587538

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.