麻豆AV

By Chris Chipello

麻豆AV researchers have discovered a cellular mechanism that may contribute to the breakdown of communication between neurons in Alzheimer鈥檚 disease.

Their study, published in Nature Communications, homes in on the role of RNA molecules involved in synaptic transmission 鈥�- the process through which neurons communicate with each other. In the brain tissue of Alzheimer鈥檚 patients, the RNAs that encode synaptic proteins are degraded more rapidly than in healthy brain cells, the researchers found. They also discovered that a protein that helps stabilize these RNAs was less abundant in the neurons of Alzheimer鈥檚 patients.

Taken together, these findings indicate that inadequate levels of the protein, known as RBFOX1, may be a factor in the faulty connections that are a hallmark of Alzheimer鈥檚 disease, says Hamed S. Najafabadi, senior author of the paper and an assistant professor in 麻豆AV鈥檚 Department of Human Genetics.

A new piece of the puzzle

Although Alzheimer鈥檚 is by far the most common form of dementia, its underlying mechanisms aren鈥檛 fully understood, and there are currently no treatments to stop its progression. The 麻豆AV study reveals a new piece of the puzzle, which could provide leads for new therapeutic approaches.

Human cells produce thousands of different types of RNAs to carry genetic information. RNAs also decay constantly, and the balance between production and degradation determines how much of a given RNA is present in the cell. Yet scientists know relatively little about how RNA decay is controlled, largely because methods of measuring degradation have been expensive and not applicable to human tissues.

Previous research by Najafabadi had shown that RNA degradation is involved in different human diseases. Most of those findings came from studies in cell line models of diseases, however. 鈥淲e wanted to directly measure the RNA degradation rate in human tissues, but available methods weren鈥檛 able to do that,鈥� Najafabadi explains. So his team hit on a way to get around that problem. 鈥淲e realized that by modeling the process of RNA production and decay, we could devise a mathematical method to calculate RNA degradation using existing genomics technologies.鈥�

Measuring RNA decay

To test their new approach, the 麻豆AV researchers enlisted the help of scientists at the University of California, San Francisco. The California team, led by Hani Goodarzi, grew cells in a lab, and measured the rate of RNA degradation using a conventional method. At the same time, the 麻豆AV researchers estimated the rate using their mathematical method. The two results matched up, validating the mathematical framework.

Najafabadi and 麻豆AV graduate student Rached Alkallas then applied the mathematical method to analyze publicly available data on the brain tissues of people who died from Alzheimer鈥檚. They also analyzed brain tissues from people who didn鈥檛 suffer from Alzheimer鈥檚. Comparing those two groups revealed the rapid rate of RNA degradation and short supply of RBFOX1 protein in the Alzheimer鈥檚 patients.