Evidence map›Paper›PMID 26047659›Full record

ArticleCellular and molecular life sciences : CMLS2015

Efficient inhibition of infectious prions multiplication and release by targeting the exosomal pathway.

Didier Vilette, Karine Laulagnier, Alvina Huor, Sandrine Alais, Sabrina Simoes, Romao Maryse, Monique Provansal, Sylvain Lehmann, Olivier Andreoletti, Laurent Schaeffer and 2 more

Open access · greenAbstract read
In one paragraph

Article in Cellular and molecular life sciences : CMLS, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
2.9field-weighted citation impact, top 9% 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

31 citing papers in PubMed, 55 citations in OpenAlex.

  1. Review
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  11. Diminished Neuronal ESCRT-0 Function Exacerbates AMPA Receptor Derangement and Accelerates Prion-Induced Neurodegeneration.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2023
    Article
  12. Article
  13. Therapeutically harnessing extracellular vesicles.Nature reviews. Drug discovery · 2022
    Review
  14. Review
  15. Article
  16. Review
  17. Function of exosomes in neurological disorders and brain tumors.Extracellular vesicles and circulating nucleic acids · 2021
    Article
  18. A New Take on Prion Protein Dynamics in Cellular Trafficking.International journal of molecular sciences · 2020
    Review
  19. Article
  20. Review
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 4 institutions in 1 country.

Didier ViletteUMR INRA/ENVT 1225, Interactions Hôte Agent Pathogène, Toulouse, France. d.vilette@envt.fr.
Karine LaulagnierCNRS, UMR5239, Laboratoire de Biologie Moléculaire de la Cellule (LBMC), ENS Lyon, 46 allée d'Italie, 69364, Lyon 7, France.
Alvina HuorUMR INRA/ENVT 1225, Interactions Hôte Agent Pathogène, Toulouse, France.
Sandrine AlaisCentre International de Recherche en Infectiologie (CIRI), INSERM U1111, CNRS UMR5308, UCBL, ENS Lyon, Lyon, France.
Sabrina SimoesInstitut Curie, CNRS-UMR144-Structure and Membrane Compartments, 26 rue d'Ulm, 75248, Paris Cedex 05, France.
Romao MaryseInstitut Curie, CNRS-UMR144-Structure and Membrane Compartments, 26 rue d'Ulm, 75248, Paris Cedex 05, France.
Monique ProvansalInstitut de Médecine Régénératrice et de Biothérapie (I.M.R.B.), Physiopathologie, diagnostic et thérapie cellulaire des affections neurodégénératives, INSERM Université Montpellier 1 U1040 CHU de Montpellier, Université Montpellier 1, Montpellier, France.
Sylvain LehmannInstitut de Médecine Régénératrice et de Biothérapie (I.M.R.B.), Physiopathologie, diagnostic et thérapie cellulaire des affections neurodégénératives, INSERM Université Montpellier 1 U1040 CHU de Montpellier, Université Montpellier 1, Montpellier, France.
Olivier AndreolettiUMR INRA/ENVT 1225, Interactions Hôte Agent Pathogène, Toulouse, France.
Laurent SchaefferCNRS, UMR5239, Laboratoire de Biologie Moléculaire de la Cellule (LBMC), ENS Lyon, 46 allée d'Italie, 69364, Lyon 7, France.
Graça RaposoInstitut Curie, CNRS-UMR144-Structure and Membrane Compartments, 26 rue d'Ulm, 75248, Paris Cedex 05, France.
Pascal LeblancCNRS, UMR5239, Laboratoire de Biologie Moléculaire de la Cellule (LBMC), ENS Lyon, 46 allée d'Italie, 69364, Lyon 7, France. Pascal.Leblanc@ens-lyon.fr.
Université Claude Bernard Lyon 1 · FRCentre National de la Recherche Scientifique · FRÉcole Nationale Vétérinaire de Toulouse · FRInserm · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Exosomes are secreted membrane vesicles of endosomal origin present in biological fluids. Exosomes may serve as shuttles for amyloidogenic proteins, notably infectious prions, and may participate in their spreading in vivo. To explore the significance of the exosome pathway on prion infectivity and release, we investigated the role of the endosomal sorting complex required for transport (ESCRT) machinery and the need for ceramide, both involved in exosome biogenesis. Silencing of HRS-ESCRT-0 subunit drastically impairs the formation of cellular infectious prion due to an altered trafficking of cholesterol. Depletion of Tsg101-ESCRT-I subunit or impairment of the production of ceramide significantly strongly decreases infectious prion release. Together, our data reveal that ESCRT-dependent and -independent pathways can concomitantly regulate the exosomal secretion of infectious prion, showing that both pathways operate for the exosomal trafficking of a particular cargo. These data open up a new avenue to regulate prion release and propagation.

Indexed as

Aniline CompoundsAnimalsBenzylidene CompoundsCell LineCell Line, TumorCeramidesDNA-Binding ProteinsEndosomal Sorting Complexes Required for TransportExosomesHumansImmunoblottingMice, TransgenicMicroscopy, ConfocalMicroscopy, ElectronPrionsProtein TransportAniline CompoundsBenzylidene CompoundsCeramidesDNA-Binding ProteinsEndosomal Sorting Complexes Required for TransportGW 4869PrionsTranscription FactorsTsg101 ProteinCeramideCholesterolESCRTExosomesPrionsPrPresPrPSc

Identifiers

PMID26047659
PMCPMC11113226
OpenAlexW586285597

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.