Evidence map›Paper›PMID 31208994›Full record

ReviewThe Journal of cell biology2019

Clathrin-containing adhesion complexes.

John G Lock, Francesco Baschieri, Matthew C Jones, Jonathan D Humphries, Guillaume Montagnac, Staffan Strömblad, Martin J Humphries

Abstract readReview
In one paragraph

Review in The Journal of cell biology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing 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

35 citing papers in PubMed.

  1. Article
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  7. The role and regulation of integrins in cell migration and invasion.Nature reviews. Molecular cell biology · 2025
    Review
  8. Article
  9. Article
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  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Curved adhesions mediate cell attachment to soft matrix fibres in 3D.bioRxiv : the preprint server for biology · 2023
    Article
  20. 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

7 authors.

John G LockDepartment of Pathology, School of Medical Sciences, University of New South Wales, Sydney, Australia.ORCID 0000-0002-3880-4106
Francesco BaschieriInstitut National de la Santé et de la Recherche Médicale U1170, Gustave Roussy Institute, Université Paris-Saclay, Villejuif, France.ORCID 0000-0003-0218-5320
Matthew C JonesWellcome Centre for Cell-Matrix Research, Faculty of Biology, Medicine and Health, University of Manchester, Manchester, UK.ORCID 0000-0003-4723-3277
Jonathan D HumphriesWellcome Centre for Cell-Matrix Research, Faculty of Biology, Medicine and Health, University of Manchester, Manchester, UK.ORCID 0000-0002-8953-7079
Guillaume MontagnacInstitut National de la Santé et de la Recherche Médicale U1170, Gustave Roussy Institute, Université Paris-Saclay, Villejuif, France.
Staffan StrömbladDepartment of Biosciences and Nutrition, Karolinska Institutet, Huddinge, Sweden.ORCID 0000-0002-1236-6339
Martin J HumphriesWellcome Centre for Cell-Matrix Research, Faculty of Biology, Medicine and Health, University of Manchester, Manchester, UK martin.humphries@manchester.ac.uk.ORCID 0000-0002-4331-6967

Funding

Cancer Research UK 21671Cancer Research UK C13329/A21671
6 · The paper itself

Abstract

An understanding of the mechanisms whereby cell adhesion complexes (ACs) relay signals bidirectionally across the plasma membrane is necessary to interpret the role of adhesion in regulating migration, differentiation, and growth. A range of AC types has been defined, but to date all have similar compositions and are dependent on a connection to the actin cytoskeleton. Recently, a new class of AC has been reported that normally lacks association with both the cytoskeleton and integrin-associated adhesome components, but is rich in components of the clathrin-mediated endocytosis machinery. The characterization of this new type of adhesion structure, which is emphasized by mitotic cells and cells in long-term culture, identifies a hitherto underappreciated link between the adhesion machinery and clathrin structures at the plasma membrane. While this discovery has implications for how ACs are assembled and disassembled, it raises many other issues. Consequently, to increase awareness within the field, and stimulate research, we explore a number of the most significant questions below.

Indexed as

Actin CytoskeletonAnimalsCell AdhesionCell DifferentiationCell MembraneCell MovementCell ProliferationClathrinHumansMacromolecular SubstancesMitosisClathrinMacromolecular Substances

Identifiers

PMID31208994
PMCPMC6605790

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.