Evidence map›Paper›PMID 27194484›Full record

ArticleJournal of the Royal Society, Interface2016

Gradual conversion of cellular stress patterns into pre-stressed matrix architecture during in vitro tissue growth.

Cécile M Bidan, Philip Kollmannsberger, Vanessa Gering, Sebastian Ehrig, Pascal Joly, Ansgar Petersen, Viola Vogel, Peter Fratzl, John W C Dunlop

Abstract read
In one paragraph

Article in Journal of the Royal Society, Interface, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing 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

18 citing papers in PubMed.

  1. Article
  2. Mechanical Cell Interactions on Curved Interfaces.Bulletin of mathematical biology · 2025
    Article
  3. Article
  4. Acidic Osteoid Templates the Plywood Structure of Bone Tissue.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2024
    Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
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  14. Article
  15. Confocal laser scanning microscopy-a powerful tool in bone research.Wiener medizinische Wochenschrift (1946) · 2018
    Article
  16. Article
  17. Article
  18. Article
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

9 authors.

Cécile M BidanDepartment of Biomaterials, Max Planck Institute of Colloids and Interfaces, 14424 Potsdam, Germany Berlin-Brandenburg Center and School for Regenerative Therapies, Julius Wolff Institute, Charité-Universitätsmedizin, Berlin, Germany University Grenoble Alpes, LIPhy, 38000 Grenoble, France CNRS, LIPhy, 38000 Grenoble, France cecilebidan@hotmail.com.
Philip KollmannsbergerDepartment of Biomaterials, Max Planck Institute of Colloids and Interfaces, 14424 Potsdam, Germany Laboratory of Applied Mechanobiology, Department of Health Sciences and Technology (D-HEST), ETH Zürich, Switzerland.
Vanessa GeringDepartment of Biomaterials, Max Planck Institute of Colloids and Interfaces, 14424 Potsdam, Germany.
Sebastian EhrigDepartment of Biomaterials, Max Planck Institute of Colloids and Interfaces, 14424 Potsdam, Germany.
Pascal JolyBerlin-Brandenburg Center and School for Regenerative Therapies, Julius Wolff Institute, Charité-Universitätsmedizin, Berlin, Germany Wyss Institute for Biologically Inspired Engineering, Harvard University, Boston, MA, USA.
Ansgar PetersenBerlin-Brandenburg Center and School for Regenerative Therapies, Julius Wolff Institute, Charité-Universitätsmedizin, Berlin, Germany.
Viola VogelLaboratory of Applied Mechanobiology, Department of Health Sciences and Technology (D-HEST), ETH Zürich, Switzerland.
Peter FratzlDepartment of Biomaterials, Max Planck Institute of Colloids and Interfaces, 14424 Potsdam, Germany.
John W C DunlopDepartment of Biomaterials, Max Planck Institute of Colloids and Interfaces, 14424 Potsdam, Germany john.dunlop@mpikg.mpg.de.ORCID 0000-0003-2741-6383

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The complex arrangement of the extracellular matrix (ECM) produced by cells during tissue growth, healing and remodelling is fundamental to tissue function. In connective tissues, it is still unclear how both cells and the ECM become and remain organized over length scales much larger than the distance between neighbouring cells. While cytoskeletal forces are essential for assembly and organization of the early ECM, how these processes lead to a highly organized ECM in tissues such as osteoid is not clear. To clarify the role of cellular tension for the development of these ordered fibril architectures, we used an in vitro model system, where pre-osteoblastic cells produced ECM-rich tissue inside channels with millimetre-sized triangular cross sections in ceramic scaffolds. Our results suggest a mechanical handshake between actively contracting cells and ECM fibrils: the build-up of a long-range organization of cells and the ECM enables a gradual conversion of cell-generated tension to pre-straining the ECM fibrils, which reduces the work cells have to generate to keep mature tissue under tension.

Indexed as

Stress, PhysiologicalAnimalsCell LineCeramicsCytoskeletonExtracellular MatrixMiceOsteoblastsTissue Scaffoldsextracellular matrix organizationtissue growthtissue mechanics

Identifiers

PMID27194484
PMCPMC4892267

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.