| Literature DB >> 32534166 |
Sarah Louise Nickels1, Jennifer Modamio2, Bárbara Mendes-Pinheiro3, Anna Sophia Monzel2, Fay Betsou4, Jens Christian Schwamborn5.
Abstract
The study of human midbrain development and midbrain related diseases, like Parkinson's disease (PD), is limited by deficiencies in the currently available and validated laboratory models. Three dimensional midbrain organoids represent an innovative strategy to recapitulate some aspects of the complexity and physiology of the human midbrain. Nevertheless, also these novel organoid models exhibit some inherent weaknesses, including the presence of a necrotic core and batch-to-batch variability. Here we describe an optimized approach for the standardized generation of midbrain organoids that addresses these limitations, while maintaining key features of midbrain development like dopaminergic neuron and astrocyte differentiation. Moreover, we have established a novel time-efficient, fit for purpose analysis pipeline and provided proof of concept for its usage by investigating toxin induced PD.Entities:
Keywords: Brain organoid; Midbrain; Parkinson’s disease; Standardization; in vitro disease modeling
Mesh:
Year: 2020 PMID: 32534166 DOI: 10.1016/j.scr.2020.101870
Source DB: PubMed Journal: Stem Cell Res ISSN: 1873-5061 Impact factor: 2.020