Alzheimer’s could be ‘REVERSED’ as breakthrough paves the way for new treatment that offers hope to millions
SCIENTISTS investigating Alzheimer's disease have made a key breakthrough, identifying a key cellular process that drives most common cause of dementia.
American researchers say it marks a "promising" target for drug treatments aiming to slow, or even reverse, the disease's development.
A team from the Advanced Science Research Center at The City University of New York (CUNY ASRC) discovered the critical mechanism that links cellular stress in the brain to the progression of Alzheimer's.
The study, published in the journal Neuron, says the brain's primary immune cells - called microglia - play a key role in protecting the brain from the disease.
Microglia are often dubbed the brain's "first responders", but scientists say these same cells can play a double-edged role.
Some protect brain health, while others worsen neurodegeneration, spurring on Alzheimer's.
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Understanding the differences between these cells has been a research focus for Professor Pinar Ayata, the study's principal investigator.
Prof Ayata said: "We set out to answer what are the harmful microglia in Alzheimer's disease and how can we therapeutically target them.
"We pinpointed a novel neurodegenerative microglia phenotype in Alzheimer's disease characterised by a stress-related signalling pathway."
The research team discovered that activation of this stress pathway, known as the integrated stress response (ISR), causes microglia to produce and release toxic lipids.
These lipids damage neurons and oligodendrocyte progenitor cells - two cell types that are essential for brain function and are most impacted in Alzheimer's disease.
But scientists found that blocking the stress response or the formation of lipids reversed symptoms of Alzheimer's in preclinical models using mice.
Levels of these cells were twice as high in Alzheimer's patients as they were in the brains of healthy people.
Co-lead author Anna Flury - a member of Prof Ayata's lab and a Ph.D. student - said: "These findings reveal a critical link between cellular stress and the neurotoxic effects of microglia in Alzheimer's disease."
"Targeting this pathway may open up new avenues for treatment by either halting the toxic lipid production or preventing the activation of harmful microglial phenotypes."
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The research team say their study highlights the potential of developing drugs that target specific microglial populations or mechanisms triggered by stress.
Co-lead author Leen Aljayousi, a member of Prof Ayata's lab, added: "Such treatments could significantly slow or even reverse the progression of Alzheimer's disease, offering hope to millions of patients and their families."