Evidence map›Paper›PMID 20145049›Full record

ArticleBrain : a journal of neurology2010

Pharmacological prion protein silencing accelerates central nervous system autoimmune disease via T cell receptor signalling.

Wei Hu, Stefan Nessler, Bernhard Hemmer, Todd N Eagar, Lawrence P Kane, S Rutger Leliveld, Andreas Müller-Schiffmann, Anne R Gocke, Amy Lovett-Racke, Li-Hong Ben and 11 more

Open access · bronzeAbstract readComparative Study
In one paragraph

Article in Brain : a journal of neurology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
1.8field-weighted citation impact, top 16% 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

22 citing papers in PubMed, 46 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. The multiple functions of PrPJournal of molecular medicine (Berlin, Germany) · 2022
    Review
  8. Review
  9. Microglia in Prion Diseases: Angels or Demons?International journal of molecular sciences · 2020
    Review
  10. Review
  11. Physiological Functions of the Cellular Prion Protein.Frontiers in molecular biosciences · 2017
    Review
  12. Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Review
  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

21 authors at 7 institutions in 2 countries.

Wei HuDepartment of Neurology, University of Texas Southwestern Medical Center at Dallas, TX, USA.
Stefan Nessler
Bernhard Hemmer
Todd N Eagar
Lawrence P Kane
S Rutger Leliveld
Andreas Müller-Schiffmann
Anne R Gocke
Amy Lovett-Racke
Li-Hong Ben
Rehana Z Hussain
Andreas Breil
Jeffrey L Elliott
Krishna Puttaparthi
Petra D Cravens
Mahendra P Singh
Benjamin Petsch
Lothar Stitz
Michael K Racke
Carsten Korth
Olaf Stüve
The University of Texas Southwestern Medical Center · USHeinrich Heine University Düsseldorf · DEFriedrich-Loeffler-Institut · DEThe Ohio State University · USKlinikum rechts der Isar · DETechnical University of Munich · DEUniversity of Pittsburgh · US

Funding

Regulation of NF-kB by the Akt kinaseR01GM080398 · NIGMS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI KANE, LAWRENCE P. · 2007 to 2010
$1.3M
NIGMS NIH HHS R01 GM080398
6 · The paper itself

Abstract

The primary biological function of the endogenous cellular prion protein has remained unclear. We investigated its biological function in the generation of cellular immune responses using cellular prion protein gene-specific small interfering ribonucleic acid in vivo and in vitro. Our results were confirmed by blocking cellular prion protein with monovalent antibodies and by using cellular prion protein-deficient and -transgenic mice. In vivo prion protein gene-small interfering ribonucleic acid treatment effects were of limited duration, restricted to secondary lymphoid organs and resulted in a 70% reduction of cellular prion protein expression in leukocytes. Disruption of cellular prion protein signalling augmented antigen-specific activation and proliferation, and enhanced T cell receptor signalling, resulting in zeta-chain-associated protein-70 phosphorylation and nuclear factor of activated T cells/activator protein 1 transcriptional activity. In vivo prion protein gene-small interfering ribonucleic acid treatment promoted T cell differentiation towards pro-inflammatory phenotypes and increased survival of antigen-specific T cells. Cellular prion protein silencing with small interfering ribonucleic acid also resulted in the worsening of actively induced and adoptively transferred experimental autoimmune encephalomyelitis. Finally, treatment of myelin basic protein(1-11) T cell receptor transgenic mice with prion protein gene-small interfering ribonucleic acid resulted in spontaneous experimental autoimmune encephalomyelitis. Thus, central nervous system autoimmune disease was modulated at all stages of disease: the generation of the T cell effector response, the elicitation of T effector function and the perpetuation of cellular immune responses. Our findings indicate that cellular prion protein regulates T cell receptor-mediated T cell activation, differentiation and survival. Defects in autoimmunity are restricted to the immune system and not the central nervous system. Our data identify cellular prion protein as a regulator of cellular immunological homoeostasis and suggest cellular prion protein as a novel potential target for therapeutic immunomodulation.

Indexed as

AnimalsDemyelinating Autoimmune Diseases, CNSFemaleGene SilencingMiceMice, Inbred C57BLMice, TransgenicPrionsReceptors, Antigen, T-CellRNA, Small InterferingSignal TransductionPrionsReceptors, Antigen, T-CellRNA, Small Interfering

Identifiers

PMID20145049
PMCPMC2822628
OpenAlexW2061302081

What OpenQuestion holds

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LicenceCC BY-NC
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.