Evidence map›Paper›PMID 26980715›Full record

ArticleNature communications2016

Cellular forces and matrix assembly coordinate fibrous tissue repair.

Mahmut Selman Sakar, Jeroen Eyckmans, Roel Pieters, Daniel Eberli, Bradley J Nelson, Christopher S Chen

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 73 papers.

0numbers the graph read from it
0cells of the map it votes in
73citing papers in PubMed
8.1field-weighted citation impact, top 2% 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

73 citing papers in PubMed, 123 citations in OpenAlex.

  1. Article
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  8. Suspended Tissue Engineering with Assemblable Microfluidics (STEAM).bioRxiv : the preprint server for biology · 2025
    Article
  9. Review
  10. Suspended Tissue Open Microfluidic Patterning (STOMP).Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Article
  11. Suspended Tissue Open Microfluidic Patterning (STOMP).bioRxiv : the preprint server for biology · 2025
    Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. Review
  18. Article
  19. Article
  20. Article

13 more citing papers are in PubMed but not listed here.

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

6 authors at 4 institutions in 2 countries.

Mahmut Selman SakarInstitute of Robotics and Intelligent Systems, Eidgenössische Technische Hochschule Zürich, 8092 Zurich, Switzerland.
Jeroen EyckmansDepartment of Biomedical Engineering, Boston University, 36 Cummington Mall, Boston, Massachusetts 02215, USA.
Roel PietersInstitute of Robotics and Intelligent Systems, Eidgenössische Technische Hochschule Zürich, 8092 Zurich, Switzerland.
Daniel EberliLaboratory for Urologic Tissue Engineering and Stem Cell Therapy, Department of Urology, University Hospital, Zurich 8091, Switzerland.
Bradley J NelsonInstitute of Robotics and Intelligent Systems, Eidgenössische Technische Hochschule Zürich, 8092 Zurich, Switzerland.
Christopher S ChenDepartment of Biomedical Engineering, Boston University, 36 Cummington Mall, Boston, Massachusetts 02215, USA.
ETH Zurich · CHBoston University · USHarvard University · USUniversity Hospital of Zurich · CH

Funding

REGULATION OF ANGIOGENESIS BY MICROENVIRONMENTAL CUESR01EB000262 · NIBIB · UNIVERSITY OF PENNSYLVANIA · PI CHEN, CHRISTOPHER S · 2002 to 2023
$6.2M
Stiffness, cadherins, and integrins in mechanochemical signalingR01HL115553 · NHLBI · UNIVERSITY OF PENNSYLVANIA · PI ASSOIAN, RICHARD, CHEN, CHRISTOPHER S · 2013 to 2016
$2.1M
NHLBI NIH HHS HL115553NHLBI NIH HHS R01 HL115553NIBIB NIH HHS EB00262NIBIB NIH HHS R01 EB000262
6 · The paper itself

Abstract

Planar in vitro models have been invaluable tools to identify the mechanical basis of wound closure. Although these models may recapitulate closure dynamics of epithelial cell sheets, they fail to capture how a wounded fibrous tissue rebuilds its 3D architecture. Here we develop a 3D biomimetic model for soft tissue repair and demonstrate that fibroblasts ensconced in a collagen matrix rapidly close microsurgically induced defects within 24 h. Traction force microscopy and time-lapse imaging reveal that closure of gaps begins with contractility-mediated whole-tissue deformations. Subsequently, tangentially migrating fibroblasts along the wound edge tow and assemble a progressively thickening fibronectin template inside the gap that provide the substrate for cells to complete closure. Unlike previously reported mechanisms based on lamellipodial protrusions and purse-string contraction, our data reveal a mode of stromal closure in which coordination of tissue-scale deformations, matrix assembly and cell migration act together to restore 3D tissue architecture.

Indexed as

AnimalsCadherinsCell Culture TechniquesCell MovementCollagen Type IFibroblastsFibronectinsGene Knockdown TechniquesImmunohistochemistryMiceMicroscopy, Atomic ForceMicrosurgeryModels, TheoreticalNIH 3T3 CellsSoft Tissue InjuriesTime-Lapse ImagingCadherinsCdh2 protein, mouseCollagen Type IFibronectins

Identifiers

PMID26980715
PMCPMC4799373
OpenAlexW2297776087

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.