Evidence map›Paper›PMID 22016182›Full record

ArticleDevelopmental dynamics : an official publication of the American Association of Anatomists2011

A focal adhesion protein-based mechanochemical checkpoint regulates cleft progression during branching morphogenesis.

William P Daley, Joshua M Kohn, Melinda Larsen

Abstract read
In one paragraph

Article in Developmental dynamics : an official publication of the American Association of Anatomists, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
2.3field-weighted citation impact, top 13% 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

38 citing papers in PubMed, 49 citations in OpenAlex.

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  5. Review
  6. Harnessing mechanobiology for kidney organoid research.Frontiers in cell and developmental biology · 2023
    Review
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  13. Designing stem cell niches for differentiation and self-renewal.Journal of the Royal Society, Interface · 2018
    Review
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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

3 authors at 1 institution in 1 country.

William P DaleyGraduate program in Molecular, Cellular, Developmental, and Neural Biology, University at Albany, State University of New York, Albany, New York, USA.
Joshua M Kohn
Melinda Larsen
University at Albany, State University of New York · US

Funding

Modeling Dynamics of Salivery Gland Branching MorphogenesisR01DE019244 · NIDCR · STATE UNIVERSITY OF NEW YORK AT ALBANY · PI LARSEN, MELINDA, YENER, BULENT · 2008 to 2012
$1.5M
A high-resolution in situ proteomics atlas of salivary gland developmentRC1DE020402 · NIDCR · STATE UNIVERSITY OF NEW YORK AT ALBANY · PI LARSEN, MELINDA · 2009 to 2010
$602k
Engineering Functioning Salivary Glands Using Micropatterned ScaffoldsR21DE019197 · NIDCR · STATE UNIVERSITY OF NEW YORK AT ALBANY · PI LARSEN, MELINDA · 2008 to 2010
$478k
NIDCR NIH HHS DE020402NIDCR NIH HHS R01 DE019244NIDCR NIH HHS R21 DE019197NIDCR NIH HHS R21DE019197NIDCR NIH HHS RC1 DE020402
6 · The paper itself

Abstract

Cleft formation is the initial step of branching morphogenesis in many organs. We previously demonstrated that ROCK 1 regulates a nonmuscle myosin II-dependent mechanochemical checkpoint to transition initiated clefts to progressing clefts in developing submandibular salivary glands. Here, we report that ROCK-mediated integrin activation and subsequent formation of focal adhesion complexes comprise this mechanochemical checkpoint. Inhibition of ROCK1 and nonmuscle myosin II activity decreased integrin β1 activation in the cleft region and interfered with localization and activation of focal adhesion complex proteins, such as focal adhesion kinase (FAK). Inhibition of FAK activity also prevented cleft progression, by disrupting recruitment of the focal adhesion proteins talin and vinculin and subsequent fibronectin assembly in the cleft region while decreasing ERK1/2 activation. These results demonstrate that inside-out integrin signaling leading to a localized recruitment of active FAK-containing focal adhesion protein complexes generates a mechanochemical checkpoint that facilitates progression of branching morphogenesis.

Indexed as

AnimalsCells, CulturedFemaleFibronectinsFocal Adhesion Protein-Tyrosine KinasesFocal AdhesionsImmunoblottingImmunohistochemistryIntegrin beta1MiceMicroscopy, ConfocalMitogen-Activated Protein Kinase 1Mitogen-Activated Protein Kinase 3Myosin Type IIOrgan Culture TechniquesPregnancyFibronectinsFocal Adhesion Protein-Tyrosine KinasesIntegrin beta1Mitogen-Activated Protein Kinase 1Mitogen-Activated Protein Kinase 3Myosin Type IIrho-Associated KinasesRock1 protein, mouseTalinVinculin

Identifiers

PMID22016182
PMCPMC3647453
OpenAlexW2003702099

What OpenQuestion holds

Textmetadata
LicenceTDM
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.