Researchers Develop Technology to make Aged Cells Younger

Spread the love
Telomerase mRNA Reverses Senescence in Progeria Cells. Journal of the American College of Cardiology. DOI: 10.1016/j.jacc.2017.06.017

Telomerase mRNA Reverses Senescence in Progeria Cells. Journal of the American College of Cardiology. DOI: 10.1016/j.jacc.2017.06.017

John P. Cooke, M.D., Ph.D studied cells from children with progeria, a rare condition marked by rapid aging that usually robs them of the chance to live beyond their early teens. They focused on progeria, because the condition tells them a lot about aging in general that’s ultimately relevant to all of us. “These kids are dying of heart attack and stroke at 13, 14, 15 years old,” Cooke said. Although current therapies are useful, they only add a year or two, on average, to the child’s life. We wanted to do something that would improve the children’s quality of life and potentially allow them to live longer, so we set about studying their cells and seeing if we could improve the cell function.”

Cooke and his team saw that telomeres were shorter in children with progeria and thought if they could restore the telomere length, then perhaps they could improve the cell function and its ability to divide and respond to stress.
“We all have telomere erosion over time, and many of the things that happen to these children at an accelerated pace occur in all of us,” Cooke said. “What we’ve shown is that when we reverse the process of the telomere shortening in the cells from these children and lengthen them, it can reverse a lot of the problems associated with aging.”

To do this, they used RNA therapeutics. They were able to get the cells to produce telomerase, that can extend and lengthen the telomere. They did this by delivering RNA to the cells that encodes this protein. Essentially, they gave the cells the information they needed to extend the telomere via an RNA delivery system and let the cells do the rest.

Having that protein expressed in a cell for just a few days was enough to have a substantial physiologically relevant and meaningful effect on the lifespan and function of the cells. Cooke said it was a surprise to have such an effect with one exposure to the RNA telomerase. Cooke said. “We were not expecting to see such a dramatic effect on the ability of the cells to proliferate. They could function and divide more normally, and we gave them extra lifespan, as well as better function.”

The research team also compared their approach at the cellular level to the current therapies available, and Cooke said it was night and day. “We looked at many cellular markers of aging and weren’t expecting to see such a dramatic effect on them. Our approach had a much greater effect on all the markers of cellular aging,” Cooke said. “We markedly improved the ability of cells to multiply and reversed the production of inflammatory proteins. Those markers of cell aging we looked at were all reversed with the treatment in our study.”

Cooke wants to see this approach turned into something useful and says they’re going to do it quicker than expected within a few years.
“As a physician, many of the diseases I see are due to aging. It’s a major risk factor for heart and vascular diseases,” Cooke said. “About a third of the people in this country succumb to strokes and heart attacks. If we can fix that, we’ll fix a lot of diseases.”

Cooke’s work is different from what others are doing in the progeria field, because most everyone else is focusing on the genetic mutation of progeria and the abnormal protein that results from that mutation. Cooke’s team chose to focus instead on developing a method to extend the telomere in these children.
“When you see these kids, they’re like every other kid. They want to play, they want to dream. They want to grow up and be something great,” Cooke said. “But they can’t do that. They don’t have the chance. That, alone, is reason enough to pursue this approach.”

While Cooke says aging is not irreversible, it is something their work can have a beneficial effect on. “We can at least stall or slow down accelerated aging, and that’s what we’re working toward,” he said. “Our next steps are to start moving this therapy toward clinical use. We plan to do so by improving existing cell therapies. I want to develop a therapy for these children. It’s an unmet need.” https://eurekalert.org/pub_releases/2017-07/hm-rdt072517.php