Evidence map›Paper›PMID 10545503›Full record

ArticleThe Journal of cell biology1999

Molecular characterization of dendritic cell-derived exosomes. Selective accumulation of the heat shock protein hsc73.

C Théry, A Regnault, J Garin, J Wolfers, L Zitvogel, P Ricciardi-Castagnoli, G Raposo, S Amigorena

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of cell biology, 1999. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 508 papers.

0numbers the graph read from it
0cells of the map it votes in
508citing papers in PubMed
9.4field-weighted citation impact, top 1% 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

508 citing papers in PubMed, 1,052 citations in OpenAlex.

  1. Review
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  6. Engineering Magnetic Beads for Affinity Enrichment of Exosomes.Computational and structural biotechnology journal · 2026
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448 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

8 authors at 5 institutions in 2 countries.

C ThéryInstitut National de la Santé et de la Recherche Médicale, U520, Institut Curie, 75005 Paris, France.
A Regnault
J Garin
J Wolfers
L Zitvogel
P Ricciardi-Castagnoli
G Raposo
S Amigorena
Inserm · FRInstitut Gustave Roussy · FRBiologie cellulaire et Cancer · FRCommissariat à l'Énergie Atomique et aux Énergies Alternatives · FRUniversity of Milan · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Exosomes are membrane vesicles secreted by hematopoietic cells upon fusion of late multivesicular endosomes with the plasma membrane. Dendritic cell (DC)-derived exosomes induce potent antitumor immune responses in mice, resulting in the regression of established tumors (Zitvogel, L., A. Regnault, A. Lozier, J. Wolfers, C. Flament, D. Tenza, P. Ricciardi-Castagnoli, G. Raposo, and S. Amigorena. 1998. Nat. Med. 4:594-600). To unravel the molecular basis of exosome-induced immune stimulation, we now analyze the regulation of their production during DC maturation and characterize extensively their protein composition by peptide mass mapping. Exosomes contain several cytosolic proteins (including annexin II, heat shock cognate protein hsc73, and heteromeric G protein Gi2alpha), as well as different integral or peripherally associated membrane proteins (major histocompatibility complex class II, Mac-1 integrin, CD9, milk fat globule-EGF-factor VIII [MFG-E8]). MFG-E8, the major exosomal component, binds integrins expressed by DCs and macrophages, suggesting that it may be involved in exosome targeting to these professional antigen-presenting cells. Another exosome component is hsc73, a cytosolic heat shock protein (hsp) also present in DC endocytic compartments. hsc73 was shown to induce antitumor immune responses in vivo, and therefore could be involved in the exosome's potent antitumor effects. Finally, exosome production is downregulated upon DC maturation, indicating that in vivo, exosomes are produced by immature DCs in peripheral tissues. Thus, DC-derived exosomes accumulate a defined subset of cellular proteins reflecting their endosomal biogenesis and accounting for their biological function.

Indexed as

Antigens, SurfaceExocytosisHSP70 Heat-Shock ProteinsMilk ProteinsAnimalsAnnexin A2Antineoplastic AgentsCell DifferentiationCell LineCytosolDendritic CellsEndosomesHeat-Shock ProteinsHistocompatibility Antigens Class IIHSC70 Heat-Shock ProteinsIntegrinsAnnexin A2Antigens, SurfaceAntineoplastic AgentsHeat-Shock ProteinsHistocompatibility Antigens Class IIHSC70 Heat-Shock ProteinsHSP70 Heat-Shock ProteinsHspa8 protein, mouseIntegrinsMembrane GlycoproteinsMembrane ProteinsMfge8 protein, mouseMilk Proteins

Identifiers

PMID10545503
PMCPMC2151184
OpenAlexW2122635106

What OpenQuestion holds

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LicenceCC BY-NC-SA
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.