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Journal Article

Microglia are essential for tissue contraction in wound closure after brain injury in zebrafish larvae

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Wehner,  Daniel
Wehner Research Group, Guck Division, Max Planck Institute for the Science of Light, Max Planck Society;
Wehner Research Group, Guck Division, Max-Planck-Zentrum für Physik und Medizin, Max Planck Institute for the Science of Light, Max Planck Society;
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Life Sci Alliance 2024 El-Daher.pdf
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Citation

El-Daher, F., Enos, S. J., Drake, L. K., Wehner, D., Westphal, M., Porter, N. J., et al. (2024). Microglia are essential for tissue contraction in wound closure after brain injury in zebrafish larvae. Life science alliance, 8(1): e202403052. doi:10.26508/lsa.202403052.


Cite as: https://hdl.handle.net/21.11116/0000-000F-F3C2-3
Abstract
Wound closure after brain injury is crucial for tissue restoration but remains poorly understood at the tissue level. We investigated this process using in vivo observations of larval zebrafish brain injury. Our findings show that wound closure occurs within the first 24 h through global tissue contraction, as evidenced by live-imaging and drug inhibition studies. Microglia accumulate at the wound site before closure, and computational models suggest that their physical traction could drive this process. Depleting microglia genetically or pharmacologically impairs tissue repair. At the cellular level, live imaging reveals centripetal deformation of astrocytic processes contacted by migrating microglia. Laser severing of these contacts causes rapid retraction of microglial processes and slower retraction of astrocytic processes, indicating tension. Disrupting the lcp1 gene, which encodes the F-actin–stabilising protein L-plastin, in microglia results in failed wound closure. These findings support a mechanical role of microglia in wound contraction and suggest that targeting microglial mechanics could offer new strategies for treating traumatic brain injury.