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Phenotyping of Human iPSC-derived Neurons

Patient-Driven Research

  • 1st Edition - September 9, 2022
  • Latest edition
  • Editor: Elizabeth D. Buttermore
  • Language: English

Phenotyping of Human iPSC-derived Neurons: Patient-Driven Research examines the steps in a preclinical pipeline that utilizes iPSC-derived neuronal technology to better understan… Read more

Description

Phenotyping of Human iPSC-derived Neurons: Patient-Driven Research examines the steps in a preclinical pipeline that utilizes iPSC-derived neuronal technology to better understand neurological disorders and identify novel therapeutics, also providing considerations and best practices. By presenting example projects that identify phenotypes and mechanisms relevant to autism spectrum disorder and epilepsy, this book allows readers to understand what considerations are important to assess at the start of project design. Sections address reproducibility issues and advances in technology at each stage of the pipeline and provide suggestions for improvement. From patient sample collection and proper controls to neuronal differentiation, phenotyping, screening, and considerations for moving to the clinic, these detailed descriptions of each stage of the pipeline will help everyone, regardless of stage in the pipeline.

In recent years, drug discovery in the neurosciences has struggled to identify novel therapeutics for patients with varying indications, including epilepsy, chronic pain, and psychosis. Current treatment options for such patients are decades old and offer little relief with many side effects. One explanation for this lull in novel therapeutics is a lack of novel target identification for neurological disorders (and target identification requires exemplar preclinical data). To improve on the preclinical work that often relies on rodent modeling, the field has begun utilizing patient-derived induced pluripotent stem cells (iPSCs) to differentiate neurons in vitro for preclinical characterization of neurological disease and target identification.

Key features

  • Discusses techniques and new technology for iPSC culturing and neuronal differentiation to establish best practices in the lab
  • Outlines considerations for phenotypic assay development
  • Provides information about the successes, failures, and implications of phenotyping and screening with iPSC-derived neurons
  • Describes how human iPSC-derived neurons are being used for preclinical discovery research as well as the development of therapeutics utilizing hiPSC-derived neurons

Readership

Academic and industry researchers in translational neuroscience and regenerative medicine

Table of contents

Section I: Best practices and considerations when designing a new project

1. iPSC culture: best practices from sample procurement to reprogramming and differentiation

2. Phenotypic assay development with iPSC-derived neurons: technical

3. Derivation of cortical interneurons from human pluripotent stem cells to model neurodevelopmental disorders

4. Development of transcription factor-based strategies for neuronal differentiation from pluripotent stem cells

5. Differentiation of Purkinje cells from pluripotent stem cells for disease phenotyping in vitro

6. Brain organoids: models of cell type diversity, connectivity, and disease phenotypes

Section II: The use of iPSC-derived neurons to study neurological disorders

7. Human models as new tools for drug development and precision medicine

8. Use of cerebral organoids to model environmental and gene x environment interactions in the developing fetus and neurodegenerative disorders

9. iPSC-derived models of autism: Tools for patient phenotyping and assay-based drug discovery

10. Probing the electrophysiological properties of patient-derived neurons across neurodevelopmental disorders

11. Advantages and limitations of hiPSC-derived neurons for the study of neurodegeneration

Section III: New technology, industry perspective, and transitioning to the clinic

12. Developing clinically translatable screens using iPSC-derived neural cells

13. Gene editing hPSCs for modeling neurological disorders

14. Cell therapy and biomanufacturing using hiPSC-derived neurons

15. Ethical considerations for the use of stem cell-derived therapies

Product details

  • Edition: 1
  • Latest edition
  • Published: September 15, 2022
  • Language: English

About the editor

EB

Elizabeth D. Buttermore

Dr. Elizabeth Buttermore is currently the Director of Translational In Vitro Models in the Rosamund Stone Zander Translational Neuroscience Center at Boston Children’s Hospital (BCH) where she leads the Human Neuron Core and Neurological Repository Core. Elizabeth has 10 years of experience in phenotypic assay development using high content imaging and multielectrode array approaches. One of her goals at BCH is to help standardize the way the field obtains and interprets phenotypic data and to help researchers across academia and industry move their research forward. She completed her postdoctoral work in Clifford Woolf’s lab at BCH where she developed protocols for differentiating nociceptive neurons from human fibroblasts and iPSCs and used them to develop models for neuropathy and neuropathic pain. Prior to coming to BCH, Elizabeth completed her PhD in Neurobiology in 2012 at the University of North Carolina, in the lab of Manzoor Bhat, where she studied the organization and maintenance of molecular domains in myelinated axons.
Affiliations and expertise
Assistant Director for the Human Neuron Core at Boston Children’s Hospital (BCH), Phenotyping Services, USA

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