4.4 Article

Increased maturation of iPSC-derived neurons in a hydrogel-based 3D culture

期刊

JOURNAL OF NEUROSCIENCE METHODS
卷 360, 期 -, 页码 -

出版社

ELSEVIER
DOI: 10.1016/j.jneumeth.2021.109254

关键词

3D cell culture; IPSCs; IPSC-derived neurons; Hydrogel; Neuronal maturation

资金

  1. Swiss Commission for Technology and Innovation/Innosuisse [25383.1 PFLS-LS]
  2. Ectica Technologies AG, Switzerland

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Cultivating iPSC-derived excitatory neurons in 3D precast hydrogel plates results in increased neuronal maturity compared to 2D cultures, offering a simple and efficient method for studying neurological diseases.
Background: Induced pluripotent stem cells (iPSCs) can be differentiated into virtually every desired cell type, offering significant potential for modeling human diseases in vitro. A disadvantage is that iPSC-derived cells represent an immature, which presents a major limitation for modeling age-related diseases such as Alzheimer's disease. Evidence suggests that culturing iPSC neurons in a 3D environment may increase neuronal maturity. However, current 3D cell culture systems are cumbersome and time-consuming. New method: We cultured iPSC-derived excitatory neurons in 3D precast hydrogel plates and compared their maturation to 2D monolayer cultures. Comparison with existing methods: In contrast to other hydrogel-based 3D culture techniques, which require full encapsulation of cells, our hydrogel allows the seeded iPSCs and iPSC neurons to simply infiltrate the gel. Results: IPSC-neurons grew to a depth of 500 mu m into the hydrogel. Cell viability was comparable to 2D cultures over the course of three weeks, with even better neuronal survival in 3D cultures at the one-week time point. Levels of neuronal and synaptic maturation markers, namely, neural cell adhesion molecule 1 (NCAM1) and alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) receptor subunit GluR2, were strongly increased in 3D cultures. Furthermore, we identified 4-repeat (4R) tau in 3D cultures, which was not detectable in 2D cultures. Conclusions: We describe a simple, hydrogel-based method for 3D iPSC culture that can serve as a fast and drugscreening-compatible platform to identify new mechanisms and therapeutic targets for brain diseases. We further provided evidence for the increased maturation of iPSC neurons in a 3D microenvironment.

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