Evidence map›Paper›PMID 27602730›Full record

ArticleBiophysical journal2016

Fibrin Networks Support Recurring Mechanical Loads by Adapting their Structure across Multiple Scales.

Nicholas A Kurniawan, Bart E Vos, Andreas Biebricher, Gijs J L Wuite, Erwin J G Peterman, Gijsje H Koenderink

Abstract read
In one paragraph

Article in Biophysical journal, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing 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

20 citing papers in PubMed.

  1. Fibrin as a Versatile Fibrous Biopolymer.Sub-cellular biochemistry · 2026
    Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Structural control of fibrin bioactivity by mechanical deformation.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  9. Review
  10. The mechanics of fibrillar collagen extracellular matrix.Cell reports. Physical science · 2021
    Article
  11. Article
  12. Engineered Biomaterial Platforms to Study Fibrosis.Advanced healthcare materials · 2020
    Review
  13. Mechanochemical Adhesion and Plasticity in Multifiber Hydrogel Networks.Advanced materials (Deerfield Beach, Fla.) · 2020
    Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Review
  19. Buffers Strongly Modulate Fibrin Self-Assembly into Fibrous Networks.Langmuir : the ACS journal of surfaces and colloids · 2017
    Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors.

Nicholas A KurniawanDepartment of Systems Biophysics, FOM Institute AMOLF, Amsterdam, The Netherlands; Department of Biomedical Engineering, Eindhoven University of Technology, Eindhoven, The Netherlands; Institute for Complex Molecular Systems, Eindhoven University of Technology, Eindhoven, The Netherlands.
Bart E VosDepartment of Systems Biophysics, FOM Institute AMOLF, Amsterdam, The Netherlands.
Andreas BiebricherDepartment of Physics and Astronomy, Vrije Universiteit Amsterdam, Amsterdam, The Netherlands.
Gijs J L WuiteDepartment of Physics and Astronomy, Vrije Universiteit Amsterdam, Amsterdam, The Netherlands.
Erwin J G PetermanDepartment of Physics and Astronomy, Vrije Universiteit Amsterdam, Amsterdam, The Netherlands.
Gijsje H KoenderinkDepartment of Systems Biophysics, FOM Institute AMOLF, Amsterdam, The Netherlands. Electronic address: g.koenderink@amolf.nl.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Tissues and cells sustain recurring mechanical loads that span a wide range of loading amplitudes and timescales as a consequence of exposure to blood flow, muscle activity, and external impact. Both tissues and cells derive their mechanical strength from fibrous protein scaffolds, which typically have a complex hierarchical structure. In this study, we focus on a prototypical hierarchical biomaterial, fibrin, which is one of the most resilient naturally occurring biopolymers and forms the structural scaffold of blood clots. We show how fibrous networks composed of fibrin utilize irreversible changes in their hierarchical structure at different scales to maintain reversible stress stiffening up to large strains. To trace the origin of this paradoxical resilience, we systematically tuned the microstructural parameters of fibrin and used a combination of optical tweezers and fluorescence microscopy to measure the interactions of single fibrin fibers for the first time, to our knowledge. We demonstrate that fibrin networks adapt to moderate strains by remodeling at the network scale through the spontaneous formation of new bonds between fibers, whereas they adapt to high strains by plastic remodeling of the fibers themselves. This multiscale adaptation mechanism endows fibrin gels with the remarkable ability to sustain recurring loads due to shear flows and wound stretching. Our findings therefore reveal a microscopic mechanism by which tissues and cells can balance elastic nonlinearity and plasticity, and thus can provide microstructural insights into cell-driven remodeling of tissues.

Indexed as

ElasticityFibrinHumansMicroscopy, FluorescenceOptical TweezersRheologyStress, MechanicalFibrin

Identifiers

PMID27602730
PMCPMC5018126

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.