| Literature DB >> 28094018 |
Nigel Kee1, Nikolaos Volakakis2, Agnete Kirkeby3, Lina Dahl2, Helena Storvall2, Sara Nolbrant3, Laura Lahti2, Åsa K Björklund4, Linda Gillberg2, Eliza Joodmardi2, Rickard Sandberg5, Malin Parmar3, Thomas Perlmann6.
Abstract
Stem cell engineering and grafting of mesencephalic dopamine (mesDA) neurons is a promising strategy for brain repair in Parkinson's disease (PD). Refinement of differentiation protocols to optimize this approach will require deeper understanding of mesDA neuron development. Here, we studied this process using transcriptome-wide single-cell RNA sequencing of mouse neural progenitors expressing the mesDA neuron determinant Lmx1a. This approach resolved the differentiation of mesDA and neighboring neuronal lineages and revealed a remarkably close relationship between developing mesDA and subthalamic nucleus (STN) neurons, while also highlighting a distinct transcription factor set that can distinguish between them. While previous hESC mesDA differentiation protocols have relied on markers that are shared between the two lineages, we found that application of these highlighted markers can help to refine current stem cell engineering protocols, increasing the proportion of appropriately patterned mesDA progenitors. Our results, therefore, have important implications for cell replacement therapy in PD.Entities:
Keywords: Parkinson’s disease; development; dopamine; embryogenesis; graph clustering; hypothalamus; neurogenesis; single cell RNA-seq; stem cell; subthalamic nucleus
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Year: 2016 PMID: 28094018 DOI: 10.1016/j.stem.2016.10.003
Source DB: PubMed Journal: Cell Stem Cell ISSN: 1875-9777 Impact factor: 24.633