Evidence map›Paper›PMID 26686862›Full record

ArticleCellular and molecular life sciences : CMLS2016

TspanC8 tetraspanins differentially regulate the cleavage of ADAM10 substrates, Notch activation and ADAM10 membrane compartmentalization.

Stéphanie Jouannet, Julien Saint-Pol, Laurent Fernandez, Viet Nguyen, Stéphanie Charrin, Claude Boucheix, Christel Brou, Pierre-Emmanuel Milhiet, Eric Rubinstein

Open access · hybridAbstract read
In one paragraph

Article in Cellular and molecular life sciences : CMLS, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 77 papers.

0numbers the graph read from it
0cells of the map it votes in
77citing papers in PubMed
7.5field-weighted citation impact, top 2% 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

77 citing papers in PubMed, 135 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Lipid-Facilitated Opening of the ADAM10 Sheddase Revealed by Enhanced Sampling Simulations.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article
  5. Connexin 26 Functions as a Direct Transcriptional Regulator During the Cochlea Development.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article
  6. Article
  7. Tetraspanin TSP-12 and SUP-17/ADAM10 exhibit cell type-specific codependence for trafficking through the Golgi.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. A Valuable Target for Therapy: The Metalloproteinase ADAM10.Current protein & peptide science · 2025
    Review
  13. ADAM10 Expression by Ameloblasts Is Essential for Proper Enamel Formation.International journal of molecular sciences · 2024
    Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article

17 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

9 authors at 4 institutions in 1 country.

Stéphanie JouannetInserm, U935, 94807, Villejuif, France.
Julien Saint-PolInserm, U935, 94807, Villejuif, France.
Laurent FernandezInserm, U1054, 34090, Montpellier, France.
Viet NguyenUniversité Paris-Sud, Institut André Lwoff, 94807, Villejuif, France.
Stéphanie CharrinInserm, U935, 94807, Villejuif, France.
Claude BoucheixInserm, U935, 94807, Villejuif, France.
Christel BrouInstitut Pasteur, Laboratoire "Signalisation et Pathogenèse", 75015, Paris, France.
Pierre-Emmanuel MilhietInserm, U1054, 34090, Montpellier, France.
Eric RubinsteinInserm, U935, 94807, Villejuif, France. eric.rubinstein@inserm.fr.
Université Paris-Sud · FRCentre National de la Recherche Scientifique · FRInserm · FRInstitut Pasteur · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The metalloprotease ADAM10 mediates the shedding of the ectodomain of various cell membrane proteins, including APP, the precursor of the amyloid peptide Aβ, and Notch receptors following ligand binding. ADAM10 associates with the members of an evolutionary conserved subgroup of tetraspanins, referred to as TspanC8, which regulate its exit from the endoplasmic reticulum. Here we show that 4 of these TspanC8 (Tspan5, Tspan14, Tspan15 and Tspan33) which positively regulate ADAM10 surface expression levels differentially impact ADAM10-dependent Notch activation and the cleavage of several ADAM10 substrates, including APP, N-cadherin and CD44. Sucrose gradient fractionation, single molecule tracking and quantitative mass-spectrometry analysis of the repertoire of molecules co-immunoprecipitated with Tspan5, Tspan15 and ADAM10 show that these two tetraspanins differentially regulate ADAM10 membrane compartmentalization. These data represent a unique example where several tetraspanins differentially regulate the function of a common partner protein through a distinct membrane compartmentalization.

Indexed as

ADAM10 ProteinADAM ProteinsAmyloid beta-Protein PrecursorAmyloid Precursor Protein SecretasesCadherinsCell Line, TumorChromatography, High Pressure LiquidHumansHyaluronan ReceptorsImmunoprecipitationMembrane ProteinsMicroscopy, ConfocalReceptor, Notch1RNA InterferenceRNA, Small InterferingSubstrate SpecificityADAM10 ProteinADAM10 protein, humanADAM ProteinsAmyloid beta-Protein PrecursorAmyloid Precursor Protein SecretasesCadherinsHyaluronan ReceptorsMembrane ProteinsNOTCH1 protein, humanReceptor, Notch1RNA, Small InterferingTetraspaninsTSPAN14 protein, humanTSPAN15 protein, humanTSPAN33 protein, humanTSPAN5 protein, humanADAM10Ectodomain sheddingMembrane compartmentalizationMicrodomainNotchTetraspanin

Identifiers

PMID26686862
PMCPMC4819958
OpenAlexW2260460109

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.