Modelling autistic neurons with induced pluripotent stem cells

Annie Kathuria, Carlo Sala, Chiara Verpelli, Jack Price*

*Corresponding author for this work

Research output: Chapter in Book/Report/Conference proceedingChapterpeer-review

5 Citations (Scopus)

Abstract

Autism spectrum disorder (ASD) is a neurodevelopmental condition that affects more than 1% of children per current estimates. It has been characterised by the following two core behavioural phenotypes: (1) deficits in social interaction and communication and (2) repetitive behaviours, restricted interests and activities. Due to the complex nature of ASD, there are currently no effective treatments. The reason behind this is the clinical and genetic heterogeneity between affected individuals on the one hand and the lack of understanding of the underpinning pathophysiological mechanisms on the other hand. Induced pluripotent stem cells (iPSCs) are reprogrammed stem cells from adult cells. These have the capacity to self-renew and differentiate into any type of cells in the body. Therefore, human iPSCs provide a unique opportunity to study the human cellular and molecular phenotypes associated with ASD. Here, we systematically review various ASD variants and co-morbid diseases modelled using human iPSCs.

Original languageEnglish
Title of host publicationAdvances in Anatomy Embryology and Cell Biology
PublisherSpringer Verlag
Pages49-64
Number of pages16
Volume224
DOIs
Publication statusPublished - 2017

Publication series

NameAdvances in Anatomy Embryology and Cell Biology
Volume224
ISSN (Print)03015556

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