A gene mutation linked to Alzheimer’s disease alters a signaling pathway in certain immune cells of individuals with the disease, according to a new study by scientists at Weill Cornell Medicine.
The team also found that blocking the pathway with a drug that’s currently being tested in cancer clinical trials protects against many features of the condition in a preclinical model. The results could lead to new strategies to block the development of Alzheimer’s disease or slow its progression.
The study, published Dec. 1 in Science Translational Medicine, focused on microglia, immune cells of the central nervous system that are the first to respond when something goes wrong in the brain. Studies have identified many genetic variants linked to Alzheimer’s disease that are highly expressed in microglia, providing compelling evidence that alterations within these cells may play a role in the disease’s onset and progression.
“Microglia are guardians of the brain under healthy conditions, but can turn detrimental in disease conditions. Our goal is to identify how they become toxic and contribute to Alzheimer’s disease pathogenesis and whether we can identify immune modulators to reverse the toxicity without diminishing their normal protective function,” said senior author , director of the and the Burton P. and Judith B. Resnick Distinguished Professor in Neurodegenerative Diseases in the at Weill Cornell Medicine.
Alzheimer’s disease is the most prevalent neurodegenerative disease in aging, affecting approximately 46 million people worldwide. Theories point to a number of potential causes, including age-related changes in the brain, along with genetic, environmental, and lifestyle factors. These lead to the accumulation of toxic proteins in the brain – and according to recent evidence, immune system changes – that result in loss of neurons and their connections.
To examine how the brain’s immune cells may contribute to Alzheimer’s disease, Gan and her colleagues first established the molecule fingerprint of individual microglia in the brains of patients with Alzheimer’s disease who carry a mutation in the TREM2 gene that markedly elevates individual’s risk for developing Alzheimer’s disease. TREM2 is a receptor mainly expressed by microglia in the brain, and among other functions, it signals through an enzyme named AKT to modulate inflammation and metabolism.
The team then established a mouse model by combining two strains; one that carries the Alzheimer’s-linked mutation in the TREM2 gene and another that exhibits Tau aggregates, one of the major pathological hallmarks in Alzheimer brains. Both patients and mice with the mutation demonstrated memory-related deficits, and their microglia expressed high levels of inflammatory molecules and exhibited an overactive AKT signaling pathway. In the mice, inhibiting AKT with a drug called MK-2206 reversed the inflammatory properties of microglia and protected against synaptic toxicity – a type of damage to the brain’s neurons that is a hallmark of Alzheimer’s disease.
Importantly, because AKT signaling also contributes to the pathogenesis of many types of cancer, MK-2206 is currently being evaluated in multiple cancer clinical trials. Therefore, the safety of the drug is already under investigation.
“We identified a small molecule compound that has been tested in patients with cancer, readily enters the brain, potently modulates the brain’s immune responses, and protects against synaptic loss in animal models of Alzheimer’s disease,” Gan said. “Our findings support further study of this compound as a potential therapy for Alzheimer’s disease.”
Li Gan is a co-founder with equity and consultant for Aeton Therapeutics, Inc.
Tracey Hampton is a freelance writer for Weill Cornell Medicine.
