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Alzheimer’s Disease May Spread by ‘Jumping’ from One Brain Region to Another

Posted Feb 02 2012 3:00pm
If tau pathology starts in the entorhinal cortex and emanates from there, the most effective approach may be to treat Alzheimer’s the way we treat cancer—through early detection and treatment, before it has a chance to spread.

By Bob DeMarco
Alzheimer's Reading Room

The issue here is straight forward. Does abnormal tau move from neuron to neuron across synapses?

The research interests me because what we are talking about is the possibility of stopping abnormal tau before it spreads throughout the brain. Stopping the disease before it gets to the hippocampus and then into other regions of the brain.

Does this mean that beta amyloid gets Alzheimer's going, and tau spreads it throughout the brain?

For me this is exciting. Stop it, like we are now able to stop the spread of cancer. Stop it early before its too late.

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Study Shows Alzheimer’s Disease May Spread by ‘Jumping’ from One Brain Region to Another

Findings open new opportunities for studying Alzheimer’s and testing potential therapies
For decades, researchers have debated whether Alzheimer’s disease starts independently in vulnerable brain regions at different times, or if it begins in one region and then spreads to neuroanatomically connected areas.

A new study by Columbia University Medical Center (CUMC) researchers strongly supports the latter, demonstrating that abnormal tau protein, a key feature of the neurofibrillary tangles seen in the brains of those with Alzheimer’s, propagates along linked brain circuits, “jumping” from neuron to neuron.

The findings, published today in the online journal PloS One , open new opportunities for gaining a greater understanding of Alzheimer’s disease and other neurological diseases and for developing therapies to halt its progression, according to senior author Karen E. Duff, PhD, professor of pathology (in psychiatry and in the Taub Institute for Research on Alzheimer’s Disease and the Aging Brain) at CUMC and at the New York State Psychiatric Institute.

Alzheimer’s disease, the most common form of dementia, is characterized by the accumulation of plaques (composed of amyloid-beta protein) and fibrous tangles (composed of abnormal tau) in brain cells called neurons. Postmortem studies of human brains and neuroimaging studies have suggested that the disease, especially the neurofibrillary tangle pathology, begins in the entorhinal cortex, which plays a key role in memory. Then as Alzheimer’s progresses, the disease appears in anatomically linked higher brain regions.

“Earlier research, including functional MRI studies in humans, have also supported this pattern of spread,” said study coauthor Scott A. Small, MD, professor of neurology in the Sergievsky Center and in the Taub Institute for Research on Alzheimer’s Disease and the Aging Brain at CUMC. “But these various findings do not definitively show that Alzheimer’s spreads directly from one brain region to another.”

To look further into this issue, the CUMC researchers developed a novel transgenic mouse in which the gene for abnormal human tau is expressed predominantly in the entorhinal cortex. The brains of the mice were analyzed at different time points over 22 months to map the spread of abnormal tau protein.

The researchers found that as the mice aged, the abnormal human tau spread along a linked anatomical pathway, from the entorhinal cortex to the hippocampus to the neocortex. “This pattern very much follows the staging that we see at the earliest stages of human Alzheimer’s disease,” said Dr. Duff.

The researchers also found evidence suggesting that the abnormal tau protein was moving from neuron to neuron across synapses, the junctions that these cells use to communicate with each other.

The findings of the study have important implications for therapy.

“If, as our data suggest, tau pathology starts in the entorhinal cortex and emanates from there, the most effective approach may be to treat Alzheimer’s the way we treat cancer—through early detection and treatment, before it has a chance to spread,” said Dr. Small. “The best way to cure Alzheimer’s may be to identify and treat it when it is just beginning, to halt progression. It is during this early stage that the disease will be most amenable to treatment. That is the exciting clinical promise down the road.”

Treatments could conceivably target tau during it extracellular phase, as it moves from cell to cell, added Dr. Duff. “If we can find the mechanism by which tau spreads from one cell to another, we could potentially stop it from jumping across the synapses — perhaps using some type of immunotherapy. This would prevent the disease from spreading to other regions of the brain, which is associated with more severe dementia.”

The paper is titled, “Trans-synaptic Spread of Tau Pathology in vivo.” Additional contributors are Li Liu (CUMC), the first author, Valerie Drouet (CUMC), Jessica W. Wu (CUMC), Menno P. Witter (Norwegian University of Science and Technology), and Catherine Clelland (CUMC).

This research was supported by the National Institute of Neurological Disorders and Stroke, grant number R01NS074874 to KD, and by the National Institute on Aging, grant number AG025161 to SAS.

The authors declare no financial or other conflicts of interest.

The Taub Institute for Research on Alzheimer’s Disease and the Aging Brain at Columbia University Medical Center is a multidisciplinary group that has forged links between researchers and clinicians to uncover the causes of Alzheimer’s, Parkinson’s and other age-related brain diseases and discover ways to prevent and cure these diseases. It has partnered with the Gertrude H. Sergievsky Center at Columbia University Medical Center which was established by an endowment in 1977 to focus on diseases of the nervous system.

Source

Also see this interesting article in the New York Times, Path Is Found for the Spread of Alzheimer’s




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Original content Bob DeMarco, the Alzheimer's Reading Room


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