Engineered 3D-printed artificial axons

DSpace/Manakin Repository

Engineered 3D-printed artificial axons

Citable link to this page


Title: Engineered 3D-printed artificial axons
Author: Espinosa-Hoyos, Daniela; Jagielska, Anna; Homan, Kimberly A.; Du, Huifeng; Busbee, Travis; Anderson, Daniel G.; Fang, Nicholas X.; Lewis, Jennifer A.; Van Vliet, Krystyn J.

Note: Order does not necessarily reflect citation order of authors.

Citation: Espinosa-Hoyos, Daniela, Anna Jagielska, Kimberly A. Homan, Huifeng Du, Travis Busbee, Daniel G. Anderson, Nicholas X. Fang, Jennifer A. Lewis, and Krystyn J. Van Vliet. 2018. “Engineered 3D-printed artificial axons.” Scientific Reports 8 (1): 478. doi:10.1038/s41598-017-18744-6.
Full Text & Related Files:
Abstract: Myelination is critical for transduction of neuronal signals, neuron survival and normal function of the nervous system. Myelin disorders account for many debilitating neurological diseases such as multiple sclerosis and leukodystrophies. The lack of experimental models and tools to observe and manipulate this process in vitro has constrained progress in understanding and promoting myelination, and ultimately developing effective remyelination therapies. To address this problem, we developed synthetic mimics of neuronal axons, representing key geometric, mechanical, and surface chemistry components of biological axons. These artificial axons exhibit low mechanical stiffness approaching that of a human axon, over unsupported spans that facilitate engagement and wrapping by glial cells, to enable study of myelination in environments reflecting mechanical cues that neurons present in vivo. Our 3D printing approach provides the capacity to vary independently the complex features of the artificial axons that can reflect specific states of development, disease, or injury. Here, we demonstrate that oligodendrocytes’ production and wrapping of myelin depend on artificial axon stiffness, diameter, and ligand coating. This biofidelic platform provides direct visualization and quantification of myelin formation and myelinating cells’ response to both physical cues and pharmacological agents.
Published Version: doi:10.1038/s41598-017-18744-6
Other Sources:
Terms of Use: This article is made available under the terms and conditions applicable to Other Posted Material, as set forth at
Citable link to this page:
Downloads of this work:

Show full Dublin Core record

This item appears in the following Collection(s)


Search DASH

Advanced Search