Evidence map›Paper›PMID 34663953›Full record

ArticleNature materials2022

Microtubules tune mechanosensitive cell responses.

Shailaja Seetharaman, Benoit Vianay, Vanessa Roca, Aaron J Farrugia, Chiara De Pascalis, Batiste Boëda, Florent Dingli, Damarys Loew, Stéphane Vassilopoulos, Alexander Bershadsky and 2 more

Abstract read
PubMed Publisher
In one paragraph

Article in Nature materials, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 120 papers.

0numbers the graph read from it
0cells of the map it votes in
120citing papers in PubMed
12.2field-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

120 citing papers in PubMed, 191 citations in OpenAlex.

  1. Article
  2. Mechanical forces stimulate Golgi export.The Journal of cell biology · 2026
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60 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors at 5 institutions in 2 countries.

Shailaja SeetharamanCell Polarity, Migration and Cancer Unit, Institut Pasteur, UMR3691 CNRS, Equipe Labellisée Ligue Contre le Cancer, Paris, France.
Benoit VianayParis University, INSERM, CEA, Hôpital Saint Louis, Institut Universitaire d'Hematologie, Paris, France.
Vanessa RocaCell Polarity, Migration and Cancer Unit, Institut Pasteur, UMR3691 CNRS, Equipe Labellisée Ligue Contre le Cancer, Paris, France.
Aaron J FarrugiaMechanobiology Institute, National University of Singapore, Singapore, Singapore.
Chiara De PascalisCell Polarity, Migration and Cancer Unit, Institut Pasteur, UMR3691 CNRS, Equipe Labellisée Ligue Contre le Cancer, Paris, France.
Batiste BoëdaCell Polarity, Migration and Cancer Unit, Institut Pasteur, UMR3691 CNRS, Equipe Labellisée Ligue Contre le Cancer, Paris, France.
Florent DingliPSL Research University, Centre de Recherche, Laboratoire de Spectrométrie de Masse Protéomique, Institut Curie, Paris, France.ORCID http://orcid.org/0000-0002-7715-2446
Damarys LoewPSL Research University, Centre de Recherche, Laboratoire de Spectrométrie de Masse Protéomique, Institut Curie, Paris, France.ORCID http://orcid.org/0000-0002-9111-8842
Stéphane VassilopoulosSorbonne Université, INSERM UMRS 974, Institute of Myology, Paris, France.ORCID http://orcid.org/0000-0003-0172-330X
Alexander BershadskyMechanobiology Institute, National University of Singapore, Singapore, Singapore.ORCID http://orcid.org/0000-0002-9571-7375
Manuel ThéryParis University, INSERM, CEA, Hôpital Saint Louis, Institut Universitaire d'Hematologie, Paris, France.ORCID http://orcid.org/0000-0002-9968-1779
Sandrine Etienne-MannevilleCell Polarity, Migration and Cancer Unit, Institut Pasteur, UMR3691 CNRS, Equipe Labellisée Ligue Contre le Cancer, Paris, France. setienne@pasteur.fr.ORCID http://orcid.org/0000-0001-6651-3675
Centre National de la Recherche Scientifique · FRInserm · FRNational University of Singapore · SGUniversité Paris Sciences et Lettres · FRDélégation Paris 5 · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mechanotransduction is a process by which cells sense the mechanical properties of their surrounding environment and adapt accordingly to perform cellular functions such as adhesion, migration and differentiation. Integrin-mediated focal adhesions are major sites of mechanotransduction and their connection with the actomyosin network is crucial for mechanosensing as well as for the generation and transmission of forces onto the substrate. Despite having emerged as major regulators of cell adhesion and migration, the contribution of microtubules to mechanotransduction still remains elusive. Here, we show that talin- and actomyosin-dependent mechanosensing of substrate rigidity controls microtubule acetylation (a tubulin post-translational modification) by promoting the recruitment of α-tubulin acetyltransferase 1 (αTAT1) to focal adhesions. Microtubule acetylation tunes the mechanosensitivity of focal adhesions and Yes-associated protein (YAP) translocation. Microtubule acetylation, in turn, promotes the release of the guanine nucleotide exchange factor GEF-H1 from microtubules to activate RhoA, actomyosin contractility and traction forces. Our results reveal a fundamental crosstalk between microtubules and actin in mechanotransduction that contributes to mechanosensitive cell adhesion and migration.

Indexed as

Mechanotransduction, CellularMicrotubulesActin CytoskeletonCell AdhesionFocal AdhesionsTubulinTubulin

Identifiers

PMID34663953
OpenAlexW3205850006

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.