Researchers illuminate a new focal area for Parkinson’s disease therapy after demonstrating the beneficial effects of systemic clearing of senescent astrocytes.
Scientists at the Buck Institute for Research on Aging have shown that systemic clearing of senescent astrocytes prevents Parkinson’s neuropathology and associated symptoms in a mouse model of sporadic disease – the type implicated in 95 per cent of human cases.
Researchers in the Andersen lab at the Buck Institute provide a new potential therapeutic avenue for the incurable, progressive neurological disorder that affects seven to 10 million people worldwide, robbing them of the ability to control movement.
Senescent cells, which stop dividing in response to stress, secrete deleterious factors that cause tissue damage and lead to chronic inflammation. In this study, senescence was triggered by exposure to the pesticide paraquat, a neurotoxin formally linked to the development of Parkinson’s disease in farmworkers in 2011.
“While senescence has been implicated in Parkinson’s and
other neurodegenerative disease, we believe this is the first time that
clearing the inflammatory cells prevented symptoms from developing in a live
mammal,” said Julie K. Andersen, PhD, Buck professor
and senior author of the study. “We hope that the fact that we were able to do
this in a sporadic, rather than genetic, model of Parkinson’s, highlights its
relevance as a potential new way to tackle the most prevalent form of the
disease.”
This research is unusual given that it focuses on
senescence in astrocytes, so-called “helper” cells that perform a variety of
tasks, from axon guidance and synaptic support to control of the blood brain
barrier and blood flow. Despite astrocytes being the most numerous cell type
within the central nervous system, Andersen says they have been underappreciated
“stepchildren” in most basic neuroscience research.
She says the vast majority of Parkinson’s
research has focused on toxicity that directly affects specific neurons
implicated in the disease, “but no one has come up with an effective treatment
based on that approach.”
This research suggests
that senescent astrocytes may contribute to the development of the disease and
we’re excited to explore this avenue.”
The
research, led by adjunct faculty Shankar Chinta, PhD and postdoctoral fellow Georgia
Woods, PhD, showed that postmortem tissue from patients with
Parkinson’s displays increased astrocytic senescence, and that cultured human
astrocytes exposed to paraquat become senescent as well.
The
mice used in this research were six months old, the human equivalent of about
34 years of age. Andersen’s lab hopes to study the impact of astrocytic
senescence in mice at varying stages of lifespan to see if Parkinson’s can be
reversed as well as prevented. “Chronic inflammation fuelled by senescence
drives many age-related diseases and it’s quite possible that Parkinson’s is
among them,” says Andersen, who adds that astrocytic
inflammation may play a role in other neurodegenerative diseases such as
Alzheimer’s. “This model gives us a way to expand how we look at and
potentially treat a range of maladies,” she says.
https://www.drugtargetreview.com/news/29098/clearing-senescent-astrocytes-parkinsons/
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