The future of cerebral organoids in drug discovery

Semin Cell Dev Biol. 2021 Mar:111:67-73. doi: 10.1016/j.semcdb.2020.05.024. Epub 2020 Jul 9.

Abstract

Until the discovery of human embryonic stem cells and human induced pluripotent stem cells, biotechnology companies were severely limited in the number of human tissues that they could model in large-scale in vitro studies. Until this point, companies have been limited to immortalized cancer lines or a small number of primary cell types that could be extracted and expanded. Nowadays, protocols continue to be developed in the stem cell field, enabling researchers to model an ever-growing library of cell types in controlled, large-scale screens. One differentiation method in particular- cerebral organoids- shows substantial potential in the field of neuroscience and developmental neurobiology. Cerebral organoid technology is still in an early phase of development, and there are several challenges that are currently being addressed by academic and industrial researchers alike. Here we briefly describe some of the early adopters of cerebral organoids, several of the challenges that they are likely facing, and various technologies that are currently being implemented to overcome them.

Keywords: Automation; Biopharma; CRISPR; Cerebral organoids; Drug discovery; Imaging; Machine learning; Microscopy; Single cell RNA-seq.

Publication types

  • Review

MeSH terms

  • CRISPR-Cas Systems
  • Cell Differentiation
  • Cerebral Cortex / drug effects
  • Cerebral Cortex / metabolism
  • Cerebral Cortex / pathology
  • Drug Discovery / methods*
  • Drugs, Investigational / chemistry
  • Drugs, Investigational / pharmacology*
  • Humans
  • Induced Pluripotent Stem Cells / cytology
  • Induced Pluripotent Stem Cells / drug effects
  • Induced Pluripotent Stem Cells / metabolism
  • Machine Learning
  • Models, Biological*
  • Mutation
  • Nerve Tissue Proteins / genetics
  • Nerve Tissue Proteins / metabolism
  • Neurodegenerative Diseases / drug therapy*
  • Neurodegenerative Diseases / genetics
  • Neurodegenerative Diseases / metabolism
  • Neurodegenerative Diseases / pathology
  • Neurons / cytology
  • Neurons / drug effects
  • Neurons / metabolism
  • Neuroprotective Agents / chemistry
  • Neuroprotective Agents / pharmacology*
  • Organoids / drug effects*
  • Organoids / metabolism
  • Organoids / pathology
  • Sequence Analysis, RNA / methods
  • Single-Cell Analysis / methods

Substances

  • Drugs, Investigational
  • Nerve Tissue Proteins
  • Neuroprotective Agents