The Mechanical Properties of Spinal Cord Organoids Depend on Their Age and Composition

PURPOSE: Spinal cord organoids are valuable human in vitro models of development and disease. Many aspects of cell behavior and function in the spinal cord are regulated by mechanical signals, but the mechanical properties of human spinal cord organoids remain largely uncharacterized. METHODS: Here, we quantify the elastic and viscoelastic properties of human spinal cord organoids at four ages (days 51, 87, 132, and 179) using microindentation. RESULTS: = 0.49, p < 0.0001). Stress relaxation testing revealed pronounced viscoelasticity, with age-dependent increases most pronounced at short relaxation times and more modest at long relaxation times, suggesting that maturation selectively stiffens the short-time response while leaving long-time equilibrium stiffness largely unchanged. Immunohistological analysis revealed that neurofilament heavy chain (NFH) immunoreactivity increased with age and correlated significantly with effective Young's modulus, while glial fibrillary acidic protein (GFAP) immunoreactivity, despite increasing with age, did not correlate with stiffness, suggesting that neuron maturation contributes to age-dependent stiffening. CONCLUSION: These findings establish quantitative mechanical properties for human spinal cord organoids, provide age-specific material parameters for computational modeling and synthetic neural interface design, and inform the design of experiments related to assembloid interactions and durotaxis in the developing central nervous system.

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Publication Details

Journal
Annals of Biomedical Engineering
Published
2026-10-30
DOI
https://doi.org/10.1007/s10439-026-04434-w
Primary Topic
Cellular Mechanics and Interactions
Type
article
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article

The Mechanical Properties of Spinal Cord Organoids Depend on Their Age and Composition

Maria J. Quezada, John D. Finan, Yasaman Samei, Ingrid Cheung et al.
2 links
Annals of Biomedical Engineering
Cellular Mechanics and Interactions
article

The Mechanical Properties of Spinal Cord Organoids Depend on Their Age and Composition

Maria J. Quezada, John D. Finan, Yasaman Samei, Ingrid Cheung, Colin K. Franz
article en

Abstract

PURPOSE: Spinal cord organoids are valuable human in vitro models of development and disease. Many aspects of cell behavior and function in the spinal cord are regulated by mechanical signals, but the mechanical properties of human spinal cord organoids remain largely uncharacterized. METHODS: Here, we quantify the elastic and viscoelastic properties of human spinal cord organoids at four ages (days 51, 87, 132, and 179) using microindentation. RESULTS: = 0.49, p < 0.0001). Stress relaxation testing revealed pronounced viscoelasticity, with age-dependent increases most pronounced at short relaxation times and more modest at long relaxation times, suggesting that maturation selectively stiffens the short-time response while leaving long-time equilibrium stiffness largely unchanged. Immunohistological analysis revealed that neurofilament heavy chain (NFH) immunoreactivity increased with age and correlated significantly with effective Young's modulus, while glial fibrillary acidic protein (GFAP) immunoreactivity, despite increasing with age, did not correlate with stiffness, suggesting that neuron maturation contributes to age-dependent stiffening. CONCLUSION: These findings establish quantitative mechanical properties for human spinal cord organoids, provide age-specific material parameters for computational modeling and synthetic neural interface design, and inform the design of experiments related to assembloid interactions and durotaxis in the developing central nervous system.

Annals of Biomedical Engineering
Northwestern University (US), Shirley Ryan AbilityLab (US), University of Illinois Chicago (US), Northwestern Medicine (US)
Openalex Percentile: Top 16%
Cellular Mechanics and Interactions
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The Mechanical Properties of Spinal Cord Organoids Depend on Their Age and Composition — Maria J. Quezada, John D. Finan, et al. · Annals of Biomedical Engineering (2026) | TGRS Research Map | TGRS