Evidence map›Paper›PMID 40702732›Full record

ArticleBiophysical journal2026

Crumbs2 acts as a dynamic cellular sensor triggering stable podocyte cell-matrix anchorage.

Rohan Bhatia, Annika Möller-Kerutt, Sven Gerlach, Yannick Herfs, Rebecca Rixen, Hermann Pavenstädt, Bernd Hoffmann, Rudolf Merkel, Ulrich Kubitscheck, Thomas Weide and 1 more

Abstract read
In one paragraph

Article in Biophysical journal, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Rohan BhatiaClausius Institute of Physical and Theoretical Chemistry, University of Bonn, Bonn, Germany.
Annika Möller-KeruttUniversity Hospital of Muenster (UKM), Internal Medicine (MedD), Muenster, Germany.
Sven GerlachForschungszentrum Jülich GmbH, Institute of Biological Information Processing (IBI-2), Mechanobiology, Jülich, Germany.
Yannick HerfsForschungszentrum Jülich GmbH, Institute of Biological Information Processing (IBI-2), Mechanobiology, Jülich, Germany.
Rebecca RixenUniversity Hospital of Muenster (UKM), Internal Medicine (MedD), Muenster, Germany.
Hermann PavenstädtUniversity Hospital of Muenster (UKM), Internal Medicine (MedD), Muenster, Germany.
Bernd HoffmannForschungszentrum Jülich GmbH, Institute of Biological Information Processing (IBI-2), Mechanobiology, Jülich, Germany.
Rudolf MerkelForschungszentrum Jülich GmbH, Institute of Biological Information Processing (IBI-2), Mechanobiology, Jülich, Germany.
Ulrich KubitscheckClausius Institute of Physical and Theoretical Chemistry, University of Bonn, Bonn, Germany.
Thomas WeideUniversity Hospital of Muenster (UKM), Internal Medicine (MedD), Muenster, Germany.
Jan Peter SiebrasseClausius Institute of Physical and Theoretical Chemistry, University of Bonn, Bonn, Germany. Electronic address: jpsiebrasse@uni-bonn.de.

Funding

ChimeraX -- Next Generation Visualization and Analysis Software for Multiscale ModelingR01GM129325 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI FERRIN, THOMAS E · 2018 to 2025
$5.2M
NIGMS NIH HHS R01 GM129325
6 · The paper itself

Abstract

Mammalian Crumbs proteins 2 (CRB2) and CRB3 are expressed in the kidney, with CRB2 mainly found within podocytes. Here, we focused on the function of CRB2 in podocytes. We investigated the CRB2/CRB3A membrane dynamics at the podocyte-podocyte contact interface in a cell culture model. Traction force microscopy was employed to clarify whether the homophilic CRB2 interactions occur in cis or trans. Live-cell imaging revealed the effects of CRB2 and CRB3A expression on cell migration from the single-cell level to large cellular networks at long space and timescales. We found that CRB2 interacts in trans, but surprisingly does not form stable interconnections. Instead, CRB2 acts as a dynamic sensor for the cellular environment and triggers a massive reorganization of focal adhesions and the actin cytoskeleton upon contact of CRB2-positive cells resulting in a strongly increased cell-matrix anchoring. Cytoskeleton reorganization can also be triggered by CRB3A; however, the increased cell-matrix anchorage is CRB2 specific.

Indexed as

Extracellular MatrixMembrane ProteinsPodocytesAnimalsCell AdhesionCell MovementFocal AdhesionsMiceMembrane Proteins

Identifiers

PMID40702732
PMCPMC13507169

What OpenQuestion holds

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Registered trials

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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.