Evidence map›Paper›PMID 10792029›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2000

Epithelial and endothelial expression of the green fluorescent protein reporter gene under the control of bovine prion protein (PrP) gene regulatory sequences in transgenic mice.

C Lemaire-Vieille, T Schulze, V Podevin-Dimster, J Follet, Y Bailly, F Blanquet-Grossard, J P Decavel, E Heinen, J Y Cesbron

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2000. 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
3.8field-weighted citation impact, top 6% 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, 73 citations in OpenAlex.

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  14. Overexpression of PrPC by adenovirus-mediated gene targeting reduces ischemic injury in a stroke rat model.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2005
    Article
  15. Prion gene sequence variation within diverse groups of U.S. sheep, beef cattle, and deer.Mammalian genome : official journal of the International Mammalian Genome Society · 2003
    Article
  16. Article
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  18. Disease-associated prion protein in vessel walls.The American journal of pathology · 2002
    Article
  19. Review
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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

9 authors at 1 institution in 1 country.

C Lemaire-VieilleLaboratoire de Physiopathologie des Encéphalopathies Spongiformes Transmissibles, Institut National de la Santé et de la Recherche Médicale U167, Institut de Biologie de Lille, 1 Rue du Professeur Calmette, B.P. 447, France. catherine.lemaire@ibl.fr
T Schulze
V Podevin-Dimster
J Follet
Y Bailly
F Blanquet-Grossard
J P Decavel
E Heinen
J Y Cesbron
Institut Pasteur de Lille · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The expression of the cellular form of the prion protein (PrP(c)) gene is required for prion replication and neuroinvasion in transmissible spongiform encephalopathies. The identification of the cell types expressing PrP(c) is necessary to understanding how the agent replicates and spreads from peripheral sites to the central nervous system. To determine the nature of the cell types expressing PrP(c), a green fluorescent protein reporter gene was expressed in transgenic mice under the control of 6.9 kb of the bovine PrP gene regulatory sequences. It was shown that the bovine PrP gene is expressed as two populations of mRNA differing by alternative splicing of one 115-bp 5' untranslated exon in 17 different bovine tissues. The analysis of transgenic mice showed reporter gene expression in some cells that have been identified as expressing PrP, such as cerebellar Purkinje cells, lymphocytes, and keratinocytes. In addition, expression of green fluorescent protein was observed in the plexus of the enteric nervous system and in a restricted subset of cells not yet clearly identified as expressing PrP: the epithelial cells of the thymic medullary and the endothelial cells of both the mucosal capillaries of the intestine and the renal capillaries. These data provide valuable information on the distribution of PrP(c) at the cellular level and argue for roles of the epithelial and endothelial cells in the spread of infection from the periphery to the brain. Moreover, the transgenic mice described in this paper provide a model that will allow for the study of the transcriptional activity of the PrP gene promoter in response to scrapie infection.

Indexed as

Regulatory Sequences, Nucleic AcidAnimalsCattleCerebellar CortexCerebellumGenes, ReporterGreen Fluorescent ProteinsImmunohistochemistryKeratinocytesLuminescent ProteinsLymphocytesMiceMice, TransgenicMolecular Sequence DataPolymerase Chain ReactionPrionsGreen Fluorescent ProteinsLuminescent ProteinsPrionsPrPC Proteins

Identifiers

PMID10792029
PMCPMC25844
OpenAlexW1981995797

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.