Modeling axonal regeneration by changing cytoskeletal dynamics in stem cell-derived motor nerve organoids
Authors:
Open Access
- 8 February 2022
- journal article
- research article
- Published by Springer Nature in Scientific Reports
- Vol. 12 (1) , 1-13
Abstract
Oxidative stress triggers axon degeneration and cell death, leading to the development of neurodegenerative diseases. Spinal motor nerves project very long axons, increasing the burden on axonal transport and metabolism. As such, spinal motor nerves are expected to be susceptible to oxidative stress, but model systems for visualizing and investigating acutely degenerating motor axons are limited. In this study, we establish motor nerve organoids from human pluripotent stem cells (hPSCs) with properties similar to those of neuromesodermal progenitors (NMPs), a population of progenitor cells that comprise the caudal spinal cord. Three-dimensional differentiation of organoids efficiently gave rise to mature motor neurons within 18 days. Adherent organoids showed robust axon fascicles and active growth cones under normal conditions. In addition, more homogenous and efficient generation of motor neurons were achieved when organoids were dissociated into individual cells. Hydrogen peroxide-induced oxidative stress resulted in a broad range of signs of axon degeneration including the disappearance of growth cones and neurites, axon retraction, axon fragmentation and bleb formation, and apoptotic cell death, whose severity can be reliably quantifiable in our culture system. Remarkably, cytoskeletal drugs modulating actin or microtubule turnover differentially facilitated axon dynamics and increased axon regenerative potential. Taken together, our motor nerve organoid model could be potentially useful for drug screens evaluating the rearrangement of cytoskeletons in regenerating motor axons.Keywords
Funding Information
- National Research Foundation of Korea (NRF-2017M3C7A1047654, NRF-2018R1A5A1024261, NRF-2020R1A2C1006758)
- Korea Health Industry Development Institute (KHIDI HI14C3484)
- Korea Centers for Disease Control and Prevention (2020-ER6902-00)
- the GIST Research Institute (in 2021)
This publication has 41 references indexed in Scilit:
- Fasudil, a rho kinase inhibitor, limits motor neuron loss in experimental models of amyotrophic lateral sclerosisBritish Journal of Pharmacology, 2013
- Oxidative stress inhibits axonal transport: implications for neurodegenerative diseasesMolecular Neurodegeneration, 2012
- Treatment with trichostatin A initiated after disease onset delays disease progression and increases survival in a mouse model of amyotrophic lateral sclerosisExperimental Neurology, 2011
- HDAC6 is a target for protection and regeneration following injury in the nervous systemProceedings of the National Academy of Sciences, 2009
- The deacetylase HDAC6 is a novel critical component of stress granules involved in the stress responseGenes & Development, 2007
- Inhibition of Rho kinase (ROCK) increases neurite outgrowth on chondroitin sulphate proteoglycanin vitroand axonal regeneration in the adult optic nervein vivoJournal of Neurochemistry, 2007
- Trichostatin A increases SMN expression and survival in a mouse model of spinal muscular atrophyJournal of Clinical Investigation, 2007
- Conserved microtubule–actin interactions in cell movement and morphogenesisNature Cell Biology, 2003
- Epidemiology of mutations in superoxide dismutase in amyotrophic lateal sclerosisAnnals of Neurology, 1997
- Ultrastructural evidence for axon retraction during the spontaneous elimination of polyneuronal innervation of the rat soleus muscleJournal of Neurocytology, 1981