Evidence map›Paper›PMID 29099266›Full record

ArticleCell adhesion & migration2018

Calpain2 mediates Rab5-driven focal adhesion disassembly and cell migration.

Pablo A Mendoza, Patricio Silva, Jorge Díaz, Cecilia Arriagada, Jimena Canales, Oscar Cerda, Vicente A Torres

Open access · goldAbstract read
In one paragraph

Article in Cell adhesion & migration, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.8field-weighted citation impact, top 31% 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

10 citing papers in PubMed, 14 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Wnt/β-Catenin Signaling in Oral Carcinogenesis.International journal of molecular sciences · 2020
    Review
  9. Article
  10. Article
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

7 authors at 5 institutions in 1 country.

Pablo A Mendozaa Institute for Research in Dental Sciences, Faculty of Dentistry, Universidad de Chile , Santiago , Chile.
Patricio Silvaa Institute for Research in Dental Sciences, Faculty of Dentistry, Universidad de Chile , Santiago , Chile.
Jorge Díaza Institute for Research in Dental Sciences, Faculty of Dentistry, Universidad de Chile , Santiago , Chile.
Cecilia Arriagadaa Institute for Research in Dental Sciences, Faculty of Dentistry, Universidad de Chile , Santiago , Chile.
Jimena Canalese Programa de Biología Celular y Molecular , Instituto de Ciencias Biomédicas (ICBM), Facultad de Medicina, Universidad de Chile , Santiago , Chile.
Oscar Cerdae Programa de Biología Celular y Molecular , Instituto de Ciencias Biomédicas (ICBM), Facultad de Medicina, Universidad de Chile , Santiago , Chile.ORCID 0000-0003-2873-5722
Vicente A Torresa Institute for Research in Dental Sciences, Faculty of Dentistry, Universidad de Chile , Santiago , Chile.
Advanced Center for Chronic Diseases · CLUniversity of Chile · CLAustral University of Chile · CLMillennium Nucleus of Ion Channel Associated Diseases · CLUniversidad Central de Chile · CL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The early endosome protein Rab5 was recently shown to promote cell migration by enhancing focal adhesion disassembly through mechanisms that remain elusive. Focal adhesion disassembly is associated to proteolysis of talin, in a process that requires calpain2. Since calpain2 has been found at vesicles and endosomal compartments, we hypothesized that Rab5 stimulates calpain2 activity, leading to enhanced focal adhesion disassembly in migrating cells. We observed that calpain2 co-localizes with EEA1-positive early endosomes and co-immunoprecipitates with EEA1 and Rab5 in A549 lung carcinoma cells undergoing spreading, whereas Rab5 knock-down decreased the accumulation of calpain2 at early endosomal-enriched fractions. In addition, Rab5 silencing decreased calpain2 activity, as shown by cleavage of the fluorogenic substrate tBOC-LM-CMAC and the endogenous substrate talin. Accordingly, Rab5 promoted focal adhesion disassembly in a calpain2-dependent manner, as expression of GFP-Rab5 accelerated focal adhesion disassembly in nocodazole-synchronized cells, whereas pharmacological inhibition of calpain2 with N-acetyl-Leu-Leu-Met prevented both focal adhesion disassembly and cell migration induced by Rab5. In summary, these data uncover Rab5 as a novel regulator of calpain2 activity and focal adhesion proteolysis leading to cell migration.

Indexed as

CalpainCell AdhesionCell MovementEndosomesFocal AdhesionsHumansrab5 GTP-Binding ProteinsTalinCalpainCAPN2 protein, humanRAB5C protein, humanrab5 GTP-Binding ProteinsTalincalpain2early endosomefocal adhesionproteolysisRab5

Identifiers

PMID29099266
PMCPMC6149462
OpenAlexW2766296655

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.