Evidence map›Paper›PMID 23830819›Full record

ArticleCytokine2013

Ligand-independent interaction of the type I interferon receptor complex is necessary to observe its biological activity.

Christopher D Krause, Gina Digioia, Lara S Izotova, Junxia Xie, Youngsun Kim, Barbara J Schwartz, Olga V Mirochnitchenko, Sidney Pestka

Abstract read
In one paragraph

Article in Cytokine, 2013. 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
1.1field-weighted citation impact, top 22% 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, 12 citations in OpenAlex.

  1. Analyzing signaling activity and function in hematopoietic cells.The Journal of experimental medicine · 2021
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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 1 institution in 1 country.

Christopher D KrauseDepartment of Biochemistry and Molecular Biology, Robert Wood Johnson Medical School, The University of Medicine and Dentistry of New Jersey, 675 Hoes Lane West, Piscataway, NJ 08855, USA. Electronic address: christopher.d.krause@gmail.com.
Gina Digioia
Lara S Izotova
Junxia Xie
Youngsun Kim
Barbara J Schwartz
Olga V Mirochnitchenko
Sidney Pestka
Johnson University · US

Funding

Translational Regulation by the TNF Alpha AU-rich ElementP01AI057596 · NIAID · UNIV OF MED/DENT NJ-R W JOHNSON MED SCH · PI PESTKA, SIDNEY · 2004 to 2009
$8.8M
INTERFERON ALPHA/BETA RECEPTORSR01AI036450 · NIAID · UNIV OF MED/DENT NJ-R W JOHNSON MED SCH · PI PESTKA, SIDNEY · 1995 to 2004
$1.5M
Receptor-Signaling Protein Interactions in Real TimeR01AI059465 · NIAID · UNIV OF MED/DENT NJ-R W JOHNSON MED SCH · PI PESTKA, SIDNEY · 2004 to 2007
$1.4M
INTERLEUKIN 10 RECEPTOR COMPLEXR01AI043369 · NIAID · UNIV OF MED/DENT NJ-R W JOHNSON MED SCH · PI PESTKA, SIDNEY · 1999 to 2003
$593k
NIAID NIH HHS 3P01 AI057596-05S1NIAID NIH HHS AI057596NIAID NIH HHS P01 AI057596NIAID NIH HHS R01 AI036450NIAID NIH HHS R01 AI043369NIAID NIH HHS R01-AI043369NIAID NIH HHS R01 AI059465NIAID NIH HHS R01-AI059465NIAID NIH HHS R01-AI36450
6 · The paper itself

Abstract

Ectopic coexpression of the two chains of the Type I and Type III interferon (IFN) receptor complexes (IFN-αR1 and IFN-αR2c, or IFN-λR1 and IL-10R2) yielded sensitivity to IFN-alpha or IFN-lambda in only some cells. We found that IFN-αR1 and IFN-αR2c exhibit FRET only when expressed at equivalent and low levels. Expanded clonal cell lines expressing both IFN-αR1 and IFN-αR2c were sensitive to IFN-alpha only when IFN-αR1 and IFN-αR2c exhibited FRET in the absence of human IFN-alpha. Coexpression of RACK-1 or Jak1 enhanced the affinity of the interaction between IFN-αR1 and IFN-αR2c. Both IFN-αR1 and IFN-αR2c exhibited FRET with Jak1 and Tyk2. Together with data showing that disruption of the preassociation between the IFN-gamma receptor chains inhibited its biological activity, we propose that biologically active IFN receptors require ligand-independent juxtaposition of IFN receptor chains assisted by their associated cytosolic proteins.

Indexed as

Cell LineFluorescence Resonance Energy TransferGTP-Binding ProteinsHumansInterferon-alphaInterferon-gammaInterferon gamma ReceptorJanus Kinase 1Multiprotein ComplexesNeoplasm ProteinsProtein BindingReceptor, Interferon alpha-betaReceptors, Cell SurfaceReceptors for Activated C KinaseReceptors, InterferonTYK2 KinaseGTP-Binding ProteinsIFNAR1 protein, humanIFNAR2 protein, humanInterferon-alphaInterferon-gammaInterferon gamma ReceptorJAK1 protein, humanJanus Kinase 1Multiprotein ComplexesNeoplasm ProteinsRACK1 protein, humanReceptor, Interferon alpha-betaReceptors, Cell SurfaceReceptors for Activated C KinaseReceptors, InterferonTYK2 KinaseTYK2 protein, humanCiFPConfocal fluorescence spectroscopyECFPEGFPenhanced citrine fluorescent proteinenhanced cyan fluorescent proteinenhanced green fluorescent proteinenhanced yellow fluorescent proteinEYFPfluorescence resonance energy transferFRETIFNIFN-αIFN-γIFN-λinterferoninterferon-alphainterferon-gammainterferon-lambdaInterferon receptorOFPorange fluorescent proteinRACK-1receptor for activated protein kinase-1Receptor reconstitutionStFPstrawberry fluorescent protein

Identifiers

PMID23830819
PMCPMC3770802
OpenAlexW2049562836

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.