Literature DB >> 35776347

Modeling Axonal Degeneration Using Motor Nerve Organoids.

Siu Yu A Chow1,2, Yui Nakanishi1,2, Shohei Kaneda1,3, Yoshiho Ikeuchi4,5,6.   

Abstract

Degeneration of axons is characteristic of many devastating diseases including amyotrophic lateral sclerosis (ALS). However, lack of an in vitro neuronal culture system that mimics damages on nerves and axonal tracts hampered development of effective treatments. Here, we describe a method to model degeneration of motor neuron axons using motor nerve organoids that are formed with human induced pluripotent stem cells. In this protocol, motor neuron axon degeneration can be rapidly induced with chemical damages. Neuroprotective effects of compounds can be examined using the degenerated axons. This motor neuron axon bundle degeneration model should facilitate future screening for drugs against diseases affecting axon fascicles.
© 2022. The Author(s), under exclusive license to Springer Science+Business Media, LLC, part of Springer Nature.

Entities:  

Keywords:  Axonal degeneration; Induced pluripotent stem (iPS) cell; Microfluidic device; Motor neuron; Neurodegenerative disease; Organ-on-a-chip; Organoid

Mesh:

Year:  2022        PMID: 35776347     DOI: 10.1007/978-1-0716-2409-8_6

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN: 1064-3745


  2 in total

Review 1.  Modeling ALS with motor neurons derived from human induced pluripotent stem cells.

Authors:  Samuel Sances; Lucie I Bruijn; Siddharthan Chandran; Kevin Eggan; Ritchie Ho; Joseph R Klim; Matt R Livesey; Emily Lowry; Jeffrey D Macklis; David Rushton; Cameron Sadegh; Dhruv Sareen; Hynek Wichterle; Su-Chun Zhang; Clive N Svendsen
Journal:  Nat Neurosci       Date:  2016-04       Impact factor: 24.884

Review 2.  Oxidative stress and mitochondrial damage: importance in non-SOD1 ALS.

Authors:  Maria Teresa Carrì; Cristiana Valle; Francesca Bozzo; Mauro Cozzolino
Journal:  Front Cell Neurosci       Date:  2015-02-17       Impact factor: 5.505

  2 in total

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