Evidence map›Paper›PMID 23543276›Full record

ArticleCellular and molecular life sciences : CMLS2013

The unconventional secretion of stress-inducible protein 1 by a heterogeneous population of extracellular vesicles.

Glaucia N M Hajj, Camila P Arantes, Marcos Vinicios Salles Dias, Martín Roffé, Bruno Costa-Silva, Marilene H Lopes, Isabel Porto-Carreiro, Tatiana Rabachini, Flávia R Lima, Flávio H Beraldo and 4 more

Erratum issuedOpen access · bronzeAbstract read
In one paragraph

Article in Cellular and molecular life sciences : CMLS, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
2.7field-weighted citation impact, top 10% 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

41 citing papers in PubMed, 63 citations in OpenAlex.

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  19. Astrocyte-derived extracellular vesicles: Neuroreparative properties and role in the pathogenesis of neurodegenerative disorders.Journal of controlled release : official journal of the Controlled Release Society · 2020
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4 · The record

Corrections and comments

  • Erratum issued
    Prado, Marco M A [corrected to Prado, Marco A M]
5 · Who and what money

Authors and funding

14 authors at 5 institutions in 2 countries.

Glaucia N M HajjInternational Research Center, A.C. Camargo Hospital, Rua Taguá 540, São Paulo, 01508-010, Brazil.
Camila P Arantes
Marcos Vinicios Salles Dias
Martín Roffé
Bruno Costa-Silva
Marilene H Lopes
Isabel Porto-Carreiro
Tatiana Rabachini
Flávia R Lima
Flávio H Beraldo
Marco A M Prado
Marco M A Prado
Rafael Linden
Vilma R Martins
AC Camargo Hospital · BRUniversidade Federal do Rio de Janeiro · BRUniversidade de São Paulo · BRWestern University · CAInstituto Paulo Gontijo · BR

Funding

Canadian Institutes of Health Research
6 · The paper itself

Abstract

The co-chaperone stress-inducible protein 1 (STI1) is released by astrocytes, and has important neurotrophic properties upon binding to prion protein (PrP(C)). However, STI1 lacks a signal peptide and pharmacological approaches pointed that it does not follow a classical secretion mechanism. Ultracentrifugation, size exclusion chromatography, electron microscopy, vesicle labeling, and particle tracking analysis were used to identify three major types of extracellular vesicles (EVs) released from astrocytes with sizes ranging from 20-50, 100-200, and 300-400 nm. These EVs carry STI1 and present many exosomal markers, even though only a subpopulation had the typical exosomal morphology. The only protein, from those evaluated here, present exclusively in vesicles that have exosomal morphology was PrP(C). STI1 partially co-localized with Rab5 and Rab7 in endosomal compartments, and a dominant-negative for vacuolar protein sorting 4A (VPS4A), required for formation of multivesicular bodies (MVBs), impaired EV and STI1 release. Flow cytometry and PK digestion demonstrated that STI1 localized to the outer leaflet of EVs, and its association with EVs greatly increased STI1 activity upon PrP(C)-dependent neuronal signaling. These results indicate that astrocytes secrete a diverse population of EVs derived from MVBs that contain STI1 and suggest that the interaction between EVs and neuronal surface components enhances STI1-PrP(C) signaling.

Indexed as

AnimalsAstrocytesCarrier ProteinsCells, CulturedEnzyme-Linked Immunosorbent AssayFlow CytometryHeat-Shock ProteinsHippocampusImmunoblottingMicePrPC ProteinsSecretory VesiclesCarrier ProteinsHeat-Shock ProteinsPrPC ProteinsTP53INP1 protein, human

Identifiers

PMID23543276
PMCPMC11113396
OpenAlexW1993678757

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.