Evidence map›Paper›PMID 26441534›Full record

ArticleFrontiers in cellular neuroscience2015

Microglia mechanics: immune activation alters traction forces and durotaxis.

Lars Bollmann, David E Koser, Rajesh Shahapure, Hélène O B Gautier, Gerhard A Holzapfel, Giuliano Scarcelli, Malte C Gather, Elke Ulbricht, Kristian Franze

Abstract read
In one paragraph

Article in Frontiers in cellular neuroscience, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 75 papers.

0numbers the graph read from it
0cells of the map it votes in
75citing 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

75 citing papers in PubMed.

  1. Review
  2. Article
  3. Microengineered Gradient Hydrogels for Mechanobiology.Advanced healthcare materials · 2026
    Review
  4. Review
  5. Review
  6. Review
  7. Article
  8. Review
  9. Article
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  12. Article
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  14. Article
  15. International journal of molecular sciences · 2025
    Article
  16. Article
  17. Article
  18. Review
  19. Review
  20. Review

15 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

9 authors.

Lars BollmannDepartment of Physiology, Development and Neuroscience, University of Cambridge Cambridge, UK ; Faculty of Computer Science and Biomedical Engineering, Institute of Biomechanics, Graz University of Technology Graz, Austria.
David E KoserDepartment of Physiology, Development and Neuroscience, University of Cambridge Cambridge, UK ; Department of Physics, Institute for Theoretical Physics, University of Cologne Cologne, Germany.
Rajesh ShahapureDepartment of Physiology, Development and Neuroscience, University of Cambridge Cambridge, UK.
Hélène O B GautierDepartment of Physiology, Development and Neuroscience, University of Cambridge Cambridge, UK.
Gerhard A HolzapfelFaculty of Computer Science and Biomedical Engineering, Institute of Biomechanics, Graz University of Technology Graz, Austria.
Giuliano ScarcelliFischell Department of Bioengineering, University of Maryland College Park, MD, USA.
Malte C GatherScottish Universities Physics Alliance (SUPA), School of Physics and Astronomy, University of St Andrews St Andrews, UK.
Elke UlbrichtDepartment of Physiology, Development and Neuroscience, University of Cambridge Cambridge, UK.
Kristian FranzeDepartment of Physiology, Development and Neuroscience, University of Cambridge Cambridge, UK.

Funding

Medical Research Council G1100312Wellcome Trust
6 · The paper itself

Abstract

Microglial cells are key players in the primary immune response of the central nervous system. They are highly active and motile cells that chemically and mechanically interact with their environment. While the impact of chemical signaling on microglia function has been studied in much detail, the current understanding of mechanical signaling is very limited. When cultured on compliant substrates, primary microglial cells adapted their spread area, morphology, and actin cytoskeleton to the stiffness of their environment. Traction force microscopy revealed that forces exerted by microglia increase with substrate stiffness until reaching a plateau at a shear modulus of ~5 kPa. When cultured on substrates incorporating stiffness gradients, microglia preferentially migrated toward stiffer regions, a process termed durotaxis. Lipopolysaccharide-induced immune-activation of microglia led to changes in traction forces, increased migration velocities and an amplification of durotaxis. We finally developed a mathematical model connecting traction forces with the durotactic behavior of migrating microglial cells. Our results demonstrate that microglia are susceptible to mechanical signals, which could be important during central nervous system development and pathologies. Stiffness gradients in tissue surrounding neural implants such as electrodes, for example, could mechanically attract microglial cells, thus facilitating foreign body reactions detrimental to electrode functioning.

Indexed as

biased random walkCNSforeign body reactiongliosisLPSmechanotaxismigrationrandom walk

Identifiers

PMID26441534
PMCPMC4585148

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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.