Animal model opens way to test Alzheimer’s disease therapies — ScienceDaily

The model was developed by Professor John Morrison’s laboratory at the CNPRC, in collaboration with Professor Jeffrey Kordower of Rush University Medical Center and Paramita Chakrabarty, assistant professor at the University of Florida.

Alzheimer’s disease is thought to be caused by misfolding of the tau and amyloid proteins. Misfolded proteins spread through the brain, leading to inflammation and cell death. Tau protein is commonly found in neurons of the brain and central nervous system, but not elsewhere.

Researchers think that decades may elapse between the silent beginnings of the disease and the first signs of cognitive decline. Understanding what happens over these years could be key to preventing or reversing symptoms of Alzheimer’s disease. But it is difficult to study therapeutic strategies without a powerful animal model that resembles the human condition as closely as possible, Morrison said. Much research has focused on transgenic mice that express a human version of amyloid or tau proteins, but these studies have proven difficult to translate into new treatments.

New translational models needed

Humans and monkeys have two forms of the tau protein in their brains, but rodents only have one, said Danielle Beckman, postdoctoral researcher at the CNPRC and first author on the paper.

“We think the macaque is a better model, because it expresses the same versions of tau in the brain as humans do,” she said.

Mice also lack certain areas of neocortex such as prefrontal cortex, a region of the human brain that is highly vulnerable to Alzheimer’s disease. Prefrontal cortex is present in rhesus macaques and critically important for cognitive functions in both humans and monkeys. There is a critical need for new and better animal models for Alzheimer’s disease that can stand between mouse models and human clinical trials, Beckman said.

Chakrabarty and colleagues created versions of the human tau gene with mutations that would cause misfolding, wrapped in a virus particle. These vectors were injected into rhesus macaques, in a brain region called the entorhinal cortex, which is highly vulnerable in Alzheimer’s disease.

Within three months, they could see that misfolded tau proteins had spread to other parts of the animal’s brains. They found misfolding both of the introduced human mutant tau protein and of the monkey’s own tau proteins.

“The pattern of spreading demonstrated unequivocally that tau-based pathology followed the precise connections of the entorhinal cortex and that the seeding of pathological tau could pass from one region to the next through synaptic connections,” Morrison said. “This capacity to spread through brain circuits results in the damage to cortical areas responsible for higher level cognition quite distant from the entorhinal cortex,” he said.

The same team has previously established spreading of misfolded amyloid proteins in macaques, representing the very early stages of Alzheimer’s disease, by injecting short pieces of faulty amyloid. The new tau protein model likely represents a middle stage of the disease, Beckman said.

“We think that this represents a more degenerative phase, but before widespread cell death occurs,” she said.

The researchers next plan to test if behavioral changes comparable to human Alzheimer’s disease develop in the rhesus macaque model. If so, it could be used to test therapies that prevent misfolding or inflammation.

“We have been working to develop these models for the last four years,” Morrison said. “I don’t think you could do this without a large collaborative team and the extensive resources of a National Primate Research Center.”

Additional co-authors on the paper are: at the California National Primate Research Center, Sean Ott, Amanda Dao, Eric Zhou and Kristine Donis-Cox; William Janssen, Icahn School of Medicine, New York; Scott Muller, Rush University School of Medicine, Chicago. Morrison also has an appointment at the Department of Neurology, UC Davis School of Medicine.

The work was supported by the NIH through a collaboration between the Office of Research Infrastructure Programs and National Institute of Aging, and by the Alzheimer’s Association.