microglia mechanics: immune activation alters traction forces and durotaxis

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ID: 207367
2015
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Ranked #142 of 395 articles by views in macromolecular bioscience

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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 towards 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.
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ebollmann2015frontiersmicroglia Use this key to autocite in the manuscript while using SciMatic Manuscript Manager or Thesis Manager
Authors ;Lars eBollmann;Lars eBollmann;David Elias Koser;David Elias Koser;Rajesh eShahapure;Hélène O. B. Gautier;Gerhard A. Holzapfel;Giuliano eScarcelli;Malte C. Gather;Elke eUlbricht;Kristian eFranze
Journal macromolecular bioscience
Year 2015
DOI
10.3389/fncel.2015.00363
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