Cited by 141Pluripotent Stem Cells ResearchNeurogenesis and neuroplasticity mechanisms3D Printing in Biomedical Research

Rapid Induction of Cerebral Organoids From Human Induced Pluripotent Stem Cells Using a Chemically Defined Hydrogel and Defined Cell Culture Medium

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Lindborg, Beth A., Brekke, John H., Vegoe, Amanda L., Ulrich, Connor B., Haider, Kerri T., Subramaniam, Sandhya, Venhuizen, Scott L., Eide, Cindy R. +10 more·2016·Stem Cells Translational Medicine

Abstract

Tissue organoids are a promising technology that may accelerate development of the societal and NIH mandate for precision medicine. Here we describe a robust and simple method for generating cerebral organoids (cOrgs) from human pluripotent stem cells by using a chemically defined hydrogel material and chemically defined culture medium. By using no additional neural induction components, cOrgs appeared on the hydrogel surface within 10–14 days, and under static culture conditions, they attained sizes up to 3 mm in greatest dimension by day 28. Histologically, the organoids showed neural rosette and neural tube-like structures and evidence of early corticogenesis. Immunostaining and quantitative reverse-transcription polymerase chain reaction demonstrated protein and gene expression representative of forebrain, midbrain, and hindbrain development. Physiologic studies showed responses to glutamate and depolarization in many cells, consistent with neural behavior. The method of cerebral organoid generation described here facilitates access to this technology, enables scalable applications, and provides a potential pathway to translational applications where defined components are desirable. Significance: Tissue organoids are a promising technology with many potential applications, such as pharmaceutical screens and development of in vitro disease models, particularly for human polygenic conditions where animal models are insufficient. This work describes a robust and simple method for generating cerebral organoids from human induced pluripotent stem cells by using a chemically defined hydrogel material and chemically defined culture medium. This method, by virtue of its simplicity and use of defined materials, greatly facilitates access to cerebral organoid technology, enables scalable applications, and provides a potential pathway to translational applications where defined components are desirable.

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  • Protocols using medium free of neural induction signalling molecules promote generation of diverse brain regions and cell populations.

    “Some protocols build on the principles of spontaneous neural induction by using medium that is free of neural induction signalling molecules2,27. This promotes the generation of diverse brain regions and cell populations2,28,29.”
  • Hyaluronic acid and mixtures of hyaluronic acid and chitosan have been extensively used in the growth and construction of neural organoids.

    “Similarly, hyaluronic acid and mixtures of hyaluronic acid and chitosan have been extensively used in the growth and construction of neural organoids111–116.”

    From Towards organoid culture without Matrigel (2021) · cites this paper as [113]

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References 37 · Cited by 141

Research works printed but not linked: 4

  1. Berger J, Gärtner J. X-linked adrenoleuko- dystrophy: Clinical, biochemical and pathoge- netic aspects. Biochim Biophys Acta 2006;1763: 1721-1732.
  2. Orchard PJ, Lund T, Miller W et al. Chito- triosidase as a biomarker of cerebral adrenoleu- kodystrophy. J Neuroinflammation 2011;8:144.
  3. Lindborg B, Brekke JH, Scott CM et al. A novel chitosan-hyaluronan based hydro- colloid supports in vitro culture and differ- entiation of human mesenchymal stem/ stromal cells (MSC). Tissue Eng A 2015;21: 1952-1962.
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Authors
Lindborg, B. A., Brekke, J. H., Vegoe, A. L., Ulrich, C. B., Haider, K. T., Subramaniam, S., Venhuizen, S. L., Eide, C. R., Orchard, P. J., Chen, W., Wang, Q., Pelaez, F., Scott, C. M., Kokkoli, E., Keirstead, S. A., Dutton, J. R., Tolar, J., & O'Brien, T. D.
Affiliations
  • University of Minnesota (US)
  • Bioactive Regenerative Therapeutics, Inc., Two Harbors, Minnesota, USA
  • Stem Cell Institute, University of Minnesota, Minneapolis, Minnesota, USA
Venue
Stem Cells Translational Medicine
Published
2016-05-13
Volume
5
Issue
7
Pages
970-979
ISSN
  • 2157-6564 (ISSN-L)
  • 2157-6580
OpenAlex
W2369036439
Cited by
141
References
37
Citations by year
2026: 2 · 2025: 17 · 2024: 8 · 2023: 16 · 2022: 21 · 2021: 21 · 2020: 15 · 2019: 14 · 2018: 15 · 2017: 11 · 2016: 1
FWCI
7.10
Type
journal article
Language
en
Open access
Locations
  • Stem Cells Translational Medicine (publishedVersion)
  • PubMed Central (publishedVersion)
  • PubMed (publishedVersion)
Funders
  • University of Minnesota
  • National Institutes of Health (UL1TR002494)
  • National Cancer Institute (P30CA077598)
  • National Center for Advancing Translational Sciences
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Pluripotent Stem Cells Research
  • Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
  • Physical Sciences › Engineering › Biomedical Engineering › 3D Printing in Biomedical Research
Keywords
brain organoids, induced pluripotent stem cells, chemically defined medium, neural induction, cortical development, neural rosettes, neural tube, glutamate response, in vitro disease model, precision medicine
MeSH terms
Biomechanical Phenomena, Brain, Cell Differentiation, Cells, Cultured, Culture Media, Humans, Neurons, Organoids, Gene Expression, Hydrogel, Polyethylene Glycol Dimethacrylate, Tissue Culture Techniques, Induced Pluripotent Stem Cells

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