Evidence map›Paper›PMID 37997199›Full record

ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2024

Mechanical Intercellular Communication via Matrix-Borne Cell Force Transmission During Vascular Network Formation.

Christopher D Davidson, Firaol S Midekssa, Samuel J DePalma, Jordan L Kamen, William Y Wang, Danica Kristen P Jayco, Megan E Wieger, Brendon M Baker

Open access · goldAbstract read
In one paragraph

Article in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
4.2field-weighted citation impact, top 5% 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

11 citing papers in PubMed, 20 citations in OpenAlex.

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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

8 authors at 1 institution in 1 country.

Christopher D DavidsonDepartment of Biomedical Engineering, University of Michigan, Ann Arbor, MI, 48109, USA.
Firaol S MidekssaDepartment of Biomedical Engineering, University of Michigan, Ann Arbor, MI, 48109, USA.ORCID 0009-0007-2260-1690
Samuel J DePalmaDepartment of Biomedical Engineering, University of Michigan, Ann Arbor, MI, 48109, USA.ORCID 0000-0001-6708-5019
Jordan L KamenDepartment of Biomedical Engineering, University of Michigan, Ann Arbor, MI, 48109, USA.
William Y WangDepartment of Biomedical Engineering, University of Michigan, Ann Arbor, MI, 48109, USA.
Danica Kristen P JaycoDepartment of Biomedical Engineering, University of Michigan, Ann Arbor, MI, 48109, USA.
Megan E WiegerDepartment of Biomedical Engineering, University of Michigan, Ann Arbor, MI, 48109, USA.
Brendon M BakerDepartment of Biomedical Engineering, University of Michigan, Ann Arbor, MI, 48109, USA.ORCID 0000-0002-2785-1070
University of Michigan · US

Funding

Angiogenic hydrogel composites for microvascular integration of organoid graftsR01EB030474 · NIBIB · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI BAKER, BRENDON M · 2021 to 2024
$1.4M
POSTDOCTORAL TRAINING PROGRAM IN CARIES RESEARCHT32DE007026 · NIDCR · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI CHILDERS, NOEL K · 1985 to 2004
$424k
Fiber-reinforced hydrogels to guide the formation and integration of engineered microvasculatureF31HL152501 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI DAVIDSON, CHRISTOPHER DURBIN · 2020 to 2021
$53k
NHLBI NIH HHS F31 HL152501NIBIB NIH HHS R01 EB030474NIDCR NIH HHS T32 DE007026NIH HHS EB030474
6 · The paper itself

Abstract

Intercellular communication is critical to the formation and homeostatic function of all tissues. Previous work has shown that cells can communicate mechanically via the transmission of cell-generated forces through their surrounding extracellular matrix, but this process is not well understood. Here, mechanically defined, synthetic electrospun fibrous matrices are utilized in conjunction with a microfabrication-based cell patterning approach to examine mechanical intercellular communication (MIC) between endothelial cells (ECs) during their assembly into interconnected multicellular networks. It is found that cell force-mediated matrix displacements in deformable fibrous matrices underly directional extension and migration of neighboring ECs toward each other prior to the formation of stable cell-cell connections enriched with vascular endothelial cadherin (VE-cadherin). A critical role is also identified for calcium signaling mediated by focal adhesion kinase and mechanosensitive ion channels in MIC that extends to multicellular assembly of 3D vessel-like networks when ECs are embedded within fibrin hydrogels. These results illustrate a role for cell-generated forces and ECM mechanical properties in multicellular assembly of capillary-like EC networks and motivates the design of biomaterials that promote MIC for vascular tissue engineering.

Indexed as

Cell CommunicationEndothelial CellsBiocompatible MaterialsExtracellular MatrixTissue EngineeringBiocompatible Materialscalcium signalingelectrospinningendothelial cellsextracellular matrixfibrous matricesfocal adhesion kinasefocal adhesionsforce transmissionmechanical communicationmechanosensitive ion channelsPiezo1TRPV4vasculogenic assembly

Identifiers

PMID37997199
PMCPMC10797481
OpenAlexW4388982298

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.