Axons in the Chick Embryo Follow Soft Pathways Through Developing Somite Segments
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Publication Date
2022-07-08Journal Title
Frontiers in Cell and Developmental Biology
ISSN
2296-634X
Publisher
Frontiers Media SA
Type
Article
This Version
VoR
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Show full item recordCitation
Schaeffer, J., Weber, I. P., Thompson, A. J., Keynes, R. J., & Franze, K. (2022). Axons in the Chick Embryo Follow Soft Pathways Through Developing Somite Segments. Frontiers in Cell and Developmental Biology https://doi.org/10.3389/fcell.2022.917589
Abstract
<jats:p>During patterning of the peripheral nervous system, motor axons grow sequentially out of the neural tube in a segmented fashion to ensure functional integration of the motor roots between the surrounding cartilage and bones of the developing vertebrae. This segmented outgrowth is regulated by the intrinsic properties of each segment (somite) adjacent to the neural tube, and in particular by chemical repulsive guidance cues expressed in the posterior half. Yet, knockout models for such repulsive cues still display initial segmentation of outgrowing motor axons, suggesting the existence of additional, yet unknown regulatory mechanisms of axon growth segmentation. As neuronal growth is not only regulated by chemical but also by mechanical signals, we here characterized the mechanical environment of outgrowing motor axons. Using atomic force microscopy-based indentation measurements on chick embryo somite strips, we identified stiffness gradients in each segment, which precedes motor axon growth. Axon growth was restricted to the anterior, softer tissue, which showed lower cell body densities than the repulsive stiffer posterior parts at later stages. As tissue stiffness is known to regulate axon growth during development, our results suggest that motor axons also respond to periodic stiffness gradients imposed by the intrinsic mechanical properties of somites.</jats:p>
Sponsorship
JS was supported by the International Spinal Research Trust
(Nathalie Rose Barr Studentship, ref. RG71958), the
Rosetrees Trust (ref. M317), and the Cambridge
Philosophical Society (studentship to JS), and
acknowledges funding from Fondation pour la Recherche
Médicale (FRM) (postdoctoral fellowship
SPF201909009106). IW was supported by an EMBO
Long-Term Fellowship (ALTF 1263-2015; European
Commission FP7, Marie Curie Actions, LTFCOFUND
2013, GA-2013-609409), AT by the Wellcome Trust (grant
099743/Z/12/Z to AT), the Cambridge Philosophical Society
and the Cambridge Trusts (studentships to AT), and KF was
supported by the European Research Council (Consolidator
Grant 772426), the Alexander von Humboldt Foundation
(Alexander von Humboldt Professorship), and the Eunice
Kennedy Shriver National Institute Of Child Health and
Human Development of the National Institutes of Health
under Award Number R21HD080585. The content is solely
the responsibility of the authors and does not necessarily
represent the official views of the National Institutes of
Health.
Funder references
National Institute of Child Health and Human Development (R21HD080585)
European Research Council (772426)
Wellcome Trust (099743/Z/12/Z)
Identifiers
External DOI: https://doi.org/10.3389/fcell.2022.917589
This record's URL: https://www.repository.cam.ac.uk/handle/1810/339716
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