News Release

Aged neurons generated directly from skin more accurately model Parkinson’s disease

Peer-Reviewed Publication

International Society for Stem Cell Research

Induced dopaminergic neurons

image: Induced dopaminergic neurons directly reprogrammed from the skin cells of a patient with idiopathic Parkinson’s Disease view more 

Credit: Janelle Drouin-Ouellet, University of Montreal, Canada

The possibility to make virtually all cell types of the human body from induced pluripotent stem cells (iPSCs), which are embryonic-like cells generated from a patient’s skin in a process called reprogramming, has opened new avenues for disease modelling in the lab. However, one shortcoming of this technique is that the donor age-specific cellular features are erased during reprogramming, so that cells made from iPSCs typically resemble cells in the human embryo or fetus rather than cells in the adult or aged human individual. However, neurodegenerative diseases like Parkinson’s disease (PD) mainly affect older individuals and are therefore difficult to model with PSCs-derived neurons, which lack many defining features of aged neurons.

According to a recent report from Janelle Drouin-Ouellet (University of Montreal, Canada), Malin Parmar (University of Lund, Sweden) and colleagues in the journal Stem Cell Reports, one way of preserving the aged characteristics of neurons is to make them directly from the patient’s skin, without an iPSC intermediate. The researchers succeeded in turning skin cells from PD patients into so-called dopaminergic (DA) neurons, which are the type of neurons progressively lost in PD, by introducing a specific combination of neural-inducing genes into the skin cells. In contrast to the PD cells generated from iPS cells, this process of generating DA neurons directly from the skin cells preserved the aged genetic, epigenetic, and metabolic characteristics of the donor age. When compared to aged DA neurons from healthy skin donors, neurons from PD patients featured PD-specific cellular defects, which now could be modelled for the first time from sporadic PD patients which lack a known genetic mutation. With this new tool, the researchers hope to model PD-related neuronal defects from a much larger cohort of PD patients with the aim to identify identity causes of the disease as well as potential future therapies.

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