Dynamic indentation reveals differential viscoelastic properties of white matter versus gray matter-derived astrocytes upon treatment with lipopolysaccharide

Nelda Antonovaite*, Thecla A. van Wageningen, Erik J. Paardekam, Anne Marie van Dam, Davide Iannuzzi

*Corresponding author for this work

Research output: Contribution to JournalArticleAcademicpeer-review

Abstract

Astrocytes in white matter (WM) and gray matter (GM) brain regions have been reported to have different morphology and function. Previous single cell biomechanical studies have not differentiated between WM- and GM-derived samples. In this study, we explored the local viscoelastic properties of isolated astrocytes and show that astrocytes from rat brain WM-enriched areas are ~1.8 times softer than astrocytes from GM-enriched areas. Upon treatment with pro-inflammatory lipopolysaccharide, GM-derived astrocytes become significantly softer in the nuclear and the cytoplasmic regions, where the F-actin network appears rearranged, whereas WM-derived astrocytes preserve their initial mechanical features and show no alteration in the F-actin cytoskeletal network. We hypothesize that the flexibility in biomechanical properties of GM-derived astrocytes may contribute to promote regeneration of the brain under neuroinflammatory conditions.

Original languageEnglish
Article number103783
JournalJournal of the Mechanical Behavior of Biomedical Materials
Volume109
DOIs
Publication statusPublished - Sept 2020

Funding

The research leading to these results has received funding from the European Research Council under the European Union's Seventh Framework Programme ( FP/2007–2013 )/ ERC grant agreement no. [ 615170 ] and The Dutch MS Research Foundation (grant 15-904MS to A-MvD). The authors further thank M. Marrese for fruitful discussions.

FundersFunder number
Dutch MS Research Foundation15-904MS
European Research Council615170
European Research Council
Seventh Framework ProgrammeFP/2007–2013
Seventh Framework Programme

    Keywords

    • Astrocytes
    • Biomechanics
    • Inflammatory response
    • Viscoelasticity

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