Summary: Researchers have pioneered a method to enhance the generation of dopaminergic neurons, crucial for Parkinson’s disease treatment, by targeting specific receptors within the Wnt signaling pathway. Using synthetic antibodies, the team successfully directed stem cell differentiation in the midbrain to produce these key neurons, which are instrumental in brain health and depleted in Parkinson’s patients.
This new approach could lead to more effective treatments for the disease, bypassing previous methods that caused unintended effects. Promising early results in rodent models show potential for restoring motor function, setting the stage for further preclinical tests.
Key Facts:
- Innovative Targeting Method: The researchers developed synthetic antibodies to selectively activate the FZD5 receptor in the Wnt signaling pathway, improving the precision of stem cell differentiation into dopaminergic neurons.
- Promising Preclinical Results: The neurons generated through this new method closely resemble natural dopaminergic neurons and have shown potential in alleviating symptoms of Parkinson’s in rodent models.
- Potential for Clinical Application: This study opens new avenues for developing Parkinson’s treatments that are more efficient and have fewer side effects, advancing closer to clinical trials.
Source: University of Toronto
Researchers at the University of Toronto have found a way to better control the preclinical generation of key neurons depleted in Parkinson’s disease, pointing toward a new approach for a disease with no cure and few effective treatments.
The researchers used an antibody to selectively activate a receptor in a molecular signaling pathway to develop dopaminergic neurons. These neurons produce dopamine, a neurotransmitter critical to brain health.
Researchers around the world have been working to coax stem cells to differentiate into dopaminergic neurons, to replace those lost in patients living with Parkinson’s disease. But efforts have been hindered in part by an inability to target specific receptors and areas of the brain.
“We used synthetic antibodies that we had previously developed to target the Wnt signaling pathway,” said Stephane Angers, principal investigator on the study and director of the Donnelly Centre for Cellular and Molecular Biology.
“We can selectively activate this pathway to direct stem cells in the midbrain to develop into neurons by targeting specific receptors in the pathway,” said Angers, who is also a professor in the Leslie Dan Faculty of Pharmacy and the Temerty Faculty of Medicine, and holds the Charles H. Best Chair of Medical Research at U of T. “This activation method has not been explored before.”
The study was recently published in the journal Development.
Parkinson’s disease is the second-most common neurological disorder after Alzheimer’s, affecting over 100,000 Canadians. It particularly impacts older men, progressively impairing movement and causing pain as well as sleep and mental health issues.
Most previous research efforts to activate the Wnt signaling pathway have relied on a GSK3 enzyme inhibitor. This method involves multiple signaling pathways for stem cell proliferation and differentiation, which can lead to unintended effects on the newly produced neurons and activation of off-target cells.
“We developed an efficient method for stimulating stem cell differentiation to produce neural cells in the midbrain,” said Andy Yang, first author on the study and a PhD student at the Donnelly Centre.
“Moreover, cells activated via the FZD5 receptor closely resemble dopaminergic neurons of natural origin.”
Another promising finding of the study was that implanting the artificially-produced neurons in a rodent model with Parkinson’s disease led to improvement of the rodent’s locomotive impairment.
“Our next step would be to continue using rodent or other suitable models to compare the outcomes of activating the FZD5 receptor and inhibiting GSK3,” said Yang. “These experiments will confirm which method is more effective in improving symptoms of Parkinson’s disease ahead of clinical trials.”
Funding: This research was supported by the University of Toronto Medicine by Design program, which receives funding from the Canada First Research Excellence Fund, and the Canadian Institutes of Health Research.
About this neurogenesis and Parkinson’s disease research news
Author: Anika Hazra
Source: University of Toronto
Contact: Anika Hazra – University of Toronto
Image: The image is credited to Neuroscience News
Original Research: Open access.
“Exploiting spatiotemporal regulation of FZD5 during neural patterning for efficient ventral midbrain specification” by Stephane Angers et al. Development
Abstract
Exploiting spatiotemporal regulation of FZD5 during neural patterning for efficient ventral midbrain specification
The Wnt/β-catenin signaling governs anterior-posterior neural patterning during development. Current human pluripotent stem cell (hPSC) differentiation protocols use a GSK3 inhibitor to activate Wnt signaling to promote posterior neural fate specification.
However, GSK3 is a pleiotropic kinase involved in multiple signaling pathways and, as GSK3 inhibition occurs downstream in the signaling cascade, it bypasses potential opportunities for achieving specificity or regulation at the receptor level.
Additionally, the specific roles of individual FZD receptors in anterior-posterior patterning are poorly understood.
Here, we have characterized the cell surface expression of FZD receptors in neural progenitor cells with different regional identity.
Our data reveal unique upregulation of FZD5 expression in anterior neural progenitors, and this expression is downregulated as cells adopt a posterior fate.
This spatial regulation of FZD expression constitutes a previously unreported regulatory mechanism that adjusts the levels of β-catenin signaling along the anterior-posterior axis and possibly contributes to midbrain-hindbrain boundary formation.
Stimulation of Wnt/β-catenin signaling in hPSCs, using a tetravalent antibody that selectively triggers FZD5 and LRP6 clustering, leads to midbrain progenitor differentiation and gives rise to functional dopaminergic neurons in vitro and in vivo.
