Abstract
Until now, models of psychiatric diseases have typically been animal models. Whether they were to be used to further understand the pathophysiology of the disorder, or as drug discovery tools, animal models have been the choice of preference in mimicking psychiatric disorders in an experimental setting. While there have been cellular models, they have generally been lacking in validity. This situation is changing with the advent of patient-specific induced pluripotent stem cells (iPSCs). In this article, we give a methodological evaluation of the current state of the iPS technology with reference to our own work in generating patient-specific iPSCs for the study of autistic spectrum disorder (ASD). In addition, we will give a broader perspective on the validity of this technology and to what extent it can be expected to complement animal models of ASD in the coming years.
Original language | English |
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Pages (from-to) | 1079-1088 |
Number of pages | 10 |
Journal | Psychopharmacology |
Volume | 231 |
Issue number | 6 |
DOIs | |
Publication status | Published - Mar 2014 |
Keywords
- Induced pluripotent stem cells
- Autism
- SHANK3
- POSTSYNAPTIC DENSITY PROTEINS
- SINGLE POLYCISTRONIC VECTOR
- HUMAN IPS CELLS
- HUMAN KERATINOCYTES
- DELETION SYNDROME
- PURKINJE-CELLS
- SOMATIC-CELLS
- GENERATION
- DIFFERENTIATION
- EXPRESSION