Evidence map›Paper›PMID 41503212›Full record

ArticleiScience2026

LAMP2A regulates endosomal protein composition and membrane identity in exosome biogenesis.

Joao Vasco Ferreira, Luís Carvalho Ferraz, Ana da Rosa Soares, Mostafa Ejtehadifar, Ana Sofia Carvalho, Michael James Hall, Judit Morello, Hans Christian Beck, Jose Silva Ramalho, Rune Matthiesen and 1 more

Abstract read
In one paragraph

Article in iScience, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. 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

11 authors.

Joao Vasco FerreiraiNOVA4Health, NOVA Medical School|Faculdade de Ciências Médicas, NMS|FCM, Universidade NOVA de Lisboa, Lisbon, Portugal.
Luís Carvalho FerraziNOVA4Health, NOVA Medical School|Faculdade de Ciências Médicas, NMS|FCM, Universidade NOVA de Lisboa, Lisbon, Portugal.
Ana da Rosa SoaresGIMM, Gulbenkian Institute for Molecular Medicine, Edifício Egas Moniz, Avenida Professor Egas Moniz, Lisbon, Portugal.
Mostafa EjtehadifariNOVA4Health, NOVA Medical School|Faculdade de Ciências Médicas, NMS|FCM, Universidade NOVA de Lisboa, Lisbon, Portugal.
Ana Sofia CarvalhoiNOVA4Health, NOVA Medical School|Faculdade de Ciências Médicas, NMS|FCM, Universidade NOVA de Lisboa, Lisbon, Portugal.
Michael James HallGIMM, Gulbenkian Institute for Molecular Medicine, Edifício Egas Moniz, Avenida Professor Egas Moniz, Lisbon, Portugal.
Judit MorelloiNOVA4Health, NOVA Medical School|Faculdade de Ciências Médicas, NMS|FCM, Universidade NOVA de Lisboa, Lisbon, Portugal.
Hans Christian BeckCentre for Clinical Proteomics, Department of Clinical Biochemistry and Pharmacology, Odense University, Hospital, Odense, Denmark.
Jose Silva RamalhoiNOVA4Health, NOVA Medical School|Faculdade de Ciências Médicas, NMS|FCM, Universidade NOVA de Lisboa, Lisbon, Portugal.
Rune MatthieseniNOVA4Health, NOVA Medical School|Faculdade de Ciências Médicas, NMS|FCM, Universidade NOVA de Lisboa, Lisbon, Portugal.
Paulo PereiraiNOVA4Health, NOVA Medical School|Faculdade de Ciências Médicas, NMS|FCM, Universidade NOVA de Lisboa, Lisbon, Portugal.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The endolysosomal system maintains cellular homeostasis through protein degradation and the release of exosomes that mediate intercellular communication. LAMP2A, a transmembrane protein, has been implicated in selective cargo loading into exosomes, or eLLoC. Here, we investigated how LAMP2A influences endosomal protein composition and function using mass spectrometry of endosomal and exosomal fractions from human retinal pigment epithelial cells. Loss of LAMP2A changed Rab GTPase distribution, reduced cortical actin association, and shifted phosphoinositide dynamics, leading to enhanced endosomal acidification and maturation. These changes extended beyond the loss of proteins containing ExoSignals, the canonical targeting motifs, suggesting that LAMP2A contributes broadly to endosomal identity. Experimental validation confirmed that LAMP2A deficiency reprograms endosomal fate toward degradation while influencing exosome composition. These findings highlight a role for LAMP2A in coordinating membrane identity, endosomal maturation, and intercellular communication through exosomes, providing insights into mechanisms that couple endosomal remodeling with cellular signaling and clearance pathways.

Indexed as

Cell biologyMolecular biology

Identifiers

PMID41503212
PMCPMC12768870

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.