Evidence map›Paper›PMID 22291008›Full record

ArticleThe Journal of biological chemistry2012

Cloning and characterization of CD300d, a novel member of the human CD300 family of immune receptors.

Emma Comas-Casellas, Águeda Martínez-Barriocanal, Francesc Miró, Aroa Ejarque-Ortiz, Simo Schwartz, Margarita Martín, Joan Sayós

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
0.9field-weighted citation impact, top 27% 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

16 citing papers in PubMed, 20 citations in OpenAlex.

  1. Article
  2. Review
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  4. Article
  5. A novel myeloid cell in murine spleen defined through gene profiling.Journal of cellular and molecular medicine · 2019
    Article
  6. Article
  7. Article
  8. Review
  9. Functional receptor molecules CD300lf and CD300ld within the CD300 family enable murine noroviruses to infect cells.Proceedings of the National Academy of Sciences of the United States of America · 2016
    Article
  10. Article
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  13. Review
  14. Article
  15. Novel identified receptors on mast cells.Frontiers in immunology · 2012
    Article
  16. 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

7 authors at 7 institutions in 1 country.

Emma Comas-CasellasImmunobiology Group, CIBBIM-Nanomedicine Program, Hospital Universitari Vall d'Hebrón, Institut de Recerca, Universitat Autònoma de Barcelona, Barcelona 08035, Spain; Networking Research Center on Bioengineering, Biomaterials, and Nanomedicine, Instituto de Salud Carlos III, Barcelona 08035, Spain.
Águeda Martínez-BarriocanalImmunobiology Group, CIBBIM-Nanomedicine Program, Hospital Universitari Vall d'Hebrón, Institut de Recerca, Universitat Autònoma de Barcelona, Barcelona 08035, Spain; Networking Research Center on Bioengineering, Biomaterials, and Nanomedicine, Instituto de Salud Carlos III, Barcelona 08035, Spain,. Electronic address: agueda.martinez@vhir.org.
Francesc MiróGene Translation Laboratory, Institute for Research in Biomedicine, Barcelona Science Park, Barcelona 08028, Spain, and.
Aroa Ejarque-OrtizImmunobiology Group, CIBBIM-Nanomedicine Program, Hospital Universitari Vall d'Hebrón, Institut de Recerca, Universitat Autònoma de Barcelona, Barcelona 08035, Spain; Networking Research Center on Bioengineering, Biomaterials, and Nanomedicine, Instituto de Salud Carlos III, Barcelona 08035, Spain.
Simo SchwartzNetworking Research Center on Bioengineering, Biomaterials, and Nanomedicine, Instituto de Salud Carlos III, Barcelona 08035, Spain,; Drug Delivery and Targeting Group, CIBBIM-Nanomedicine Program, Hospital Universitari Vall d'Hebrón, Institut de Recerca, Universitat Autònoma de Barcelona, Barcelona 08035, Spain.
Margarita MartínBiochemistry Unit, Faculty of Medicine, Institut d'Investigacions Biomèdiques August Pi i Sunyer, University of Barcelona, Barcelona 08036, Spain.
Joan SayósImmunobiology Group, CIBBIM-Nanomedicine Program, Hospital Universitari Vall d'Hebrón, Institut de Recerca, Universitat Autònoma de Barcelona, Barcelona 08035, Spain; Networking Research Center on Bioengineering, Biomaterials, and Nanomedicine, Instituto de Salud Carlos III, Barcelona 08035, Spain,. Electronic address: joan.sayos@vhir.org.
Biomedical Research Networking Center in Bioengineering, Biomaterials and Nanomedicine · ESCIBBIM-Nanomedicine · ESInstitute for Research in Biomedicine · ESInstituto de Salud Carlos III · ESUniversitat Autònoma de Barcelona · ESUniversitat de Barcelona · ESVall d'Hebron Institut de Recerca · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Herein we present the cloning and molecular characterization of CD300d, a member of the human CD300 family of immune receptors. CD300d cDNA was cloned from RNA obtained from human peripheral blood mononuclear cells, and RT-PCR revealed the gene to be expressed in cells of myeloid lineage. The cloned cDNA encoded for a type I protein with a single extracellular Ig V-type domain and a predicted molecular mass of 21.5 kDa. The short cytoplasmic tail is lacking in any known signaling motif, but there is a negatively charged residue (glutamic acid) within the transmembrane domain. CD300d forms complexes with the CD300 family members, with the exception of CD300c. Contrary to other activating members of the CD300 family of receptors, surface expression of CD300d in COS-7-transfected cells required the presence of an immunoreceptor tyrosine-based activating motif-bearing adaptor (FcεRγ). Accordingly, we found that CD300d was able to recruit FcεRγ. Unexpectedly, we could not detect CD300d on the surface of cells expressing FcεRγ, suggesting the existence of unknown mechanisms regulating the trafficking of this molecule. The presence of other CD300 molecules also did not modify the intracellular expression of CD300d. In fact, the presence of CD300d decreased the levels of surface expression of CD300f but not CD300c. Our data suggest that the function of CD300d would be related to the regulation of the expression of other CD300 molecules and the composition of CD300 complexes on the cell surface.

Indexed as

Amino Acid MotifsAmino Acid SequenceAnimalsChlorocebus aethiopsCloning, MolecularCOS CellsDNA, ComplementaryGene Expression RegulationHeLa CellsHumansLeukocytes, MononuclearMolecular Sequence DataMultiprotein ComplexesProtein Structure, TertiaryProtein TransportReceptors, IgECD300LD protein, humanDNA, ComplementaryFcepsilonRI gamma-chain, humanMultiprotein ComplexesReceptors, IgEReceptors, Immunologic

Identifiers

PMID22291008
PMCPMC3322970
OpenAlexW2134100566

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.