Evidence map›Paper›PMID 9321385›Full record

ArticleThe EMBO journal1997

Astrocyte-specific expression of hamster prion protein (PrP) renders PrP knockout mice susceptible to hamster scrapie.

A J Raeber, R E Race, S Brandner, S A Priola, A Sailer, R A Bessen, L Mucke, J Manson, A Aguzzi, M B Oldstone and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in The EMBO journal, 1997. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 76 papers.

0numbers the graph read from it
0cells of the map it votes in
76citing papers in PubMed
3.9field-weighted citation impact, top 5% 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

76 citing papers in PubMed, 210 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Article
  5. Review
  6. Review
  7. Mechanisms of prion-induced toxicity.Cell and tissue research · 2023
    Review
  8. Article
  9. Article
  10. Astrocyte in prion disease: a double-edged sword.Neural regeneration research · 2022
    Review
  11. Review
  12. Review
  13. Neuroinflammation in Prion Disease.International journal of molecular sciences · 2021
    Review
  14. Article
  15. Review
  16. Review
  17. Article
  18. Article
  19. Complement 3Acta neuropathologica communications · 2019
    Article
  20. Article

16 more citing papers are in PubMed but not listed here.

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

12 authors at 1 institution in 1 country.

A J RaeberInstitut für Molekularbiologie, Abteilung I, University of Zürich, H-onggerberg, 8093 Z-urich, Switzerland.
R E Race
S Brandner
S A Priola
A Sailer
R A Bessen
L Mucke
J Manson
A Aguzzi
M B Oldstone
C Weissmann
B Chesebro
University of Zurich · CH

Funding

VIROLOGY AND IMMUNOLOGY OF AGINGP01AG004342 · NIA · SCRIPPS RESEARCH INSTITUTE, THE · PI OLDSTONE, MICHAEL B · 1985 to 2008
$12.9M
NIA NIH HHS AG04342
6 · The paper itself

Abstract

Transmissible spongiform encephalopathies are characterized by spongiosis, astrocytosis and accumulation of PrPSc, an isoform of the normal host protein PrPC. The exact cell types responsible for agent propagation and pathogenesis are still uncertain. To determine the possible role of astrocytes, we generated mice devoid of murine PrP but expressing hamster PrP transgenes driven by the astrocyte-specific GFAP promoter. After inoculation with hamster scrapie, these mice accumulated infectivity and PrPSc to high levels, developed severe disease after 227 +/- 5 days and died 7 +/- 4 days later. Therefore, astrocytes could play an important role in scrapie pathogenesis, possibly by an indirect toxic effect on neurons. Interestingly, mice expressing the same transgenes but also endogenous murine PrP genes propagated infectivity without developing disease.

Indexed as

AnimalsAstrocytesBiological AssayBrainCricetinaeDisease SusceptibilityGlial Fibrillary Acidic ProteinMiceMice, KnockoutPrionsPrPSc ProteinsRecombinant Fusion ProteinsRNA, MessengerRodent DiseasesScrapieGlial Fibrillary Acidic ProteinPrionsPrPSc ProteinsRecombinant Fusion ProteinsRNA, Messenger

Identifiers

PMID9321385
PMCPMC1326289
OpenAlexW2125522501

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.