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Establishing preclinical models of Alzheimer’s that reflect in-life clinical symptoms of each individual is a critically important goal, yet so far it has not been fully realised. A new collaborative study from the University of Oxford has demonstrated that clinical vulnerability to an abnormally abundant protein in Alzheimer’s brain is in fact reflected in individual patient induced pluripotent stem cell-derived cortical neurons.

Synapses representing points of communication between neurons, grown in the laboratory from stem cells
Synapses, shown as green and pink dots, represent points of communication between neurons, grown in the laboratory from stem cells

Patient-specific stem cells are key to understanding Alzheimer’s. Researchers can turn stem cells into brain cells, which are not easily accessible from living patients, in the laboratory. One of the major challenges in studying these brain cells has been to model pathological changes characteristic of Alzheimer’s brains in the majority of patients who do not harbour genetic mutations that cause disease.

To tackle this issue, a collaborative study involving researchers from the University of Oxford and the clinical team from the Deep and Frequent Phenotyping cohort of early Alzheimer’s utilised blood samples donated by fourteen Alzheimer’s patients from multiple centres around the UK. The researchers converted the blood cells into stem cells before generating brain cells specific to each individual donor. Researchers then challenged these brain cells with toxic amyloid-beta - a key pathological protein in Alzheimer’s - to cause synapse loss. A loss of synapses – the junctions where brain cell communication takes place - is the strongest correlate for cognitive decline in Alzheimer's.

The team found that the extent of synapse loss varies among individual patient brain cell lines, and crucially, correlates with their clinical symptoms, such as cognitive decline or brain activity, given their varying levels of amyloid-beta burden in the brain.

Read the full story on the Department of Physiology, Anatomy and Genetics website

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