Reverting skin cells from people with a premature aging disease back to a more embryonic state appears to overcome the molecular defect in these cells. People with the disease have abnormally short telomeres, a repetitive stretch of DNA that caps chromosomes and shrinks with every cell Researchers from Children's Hospital Boston found that reprogramming the skin cells, using induced pluripotent stem cell technology, lengthened the telomeres in the cells. The reprogramming process activated the telomerase enzyme, which is responsible for maintaining telomeres. The research was published today in the online version of the journal Nature.
The research adds to previous findings suggesting that enhancing activity of the telomerase enzyme might benefit patients with premature aging disorders. The study also provides a new tool for studying telomerase, an enzyme of great interest to scientists working on both aging and cancer. The shortening of telomeres over a lifetime is thought to be tied to aging. And abnormal activation of telomerase in cancer cells allows them to proliferate uncontrollably. While scientists already knew that reprogramming could lengthen telomeres in cells from healthy people, it was unclear if the same could happen in cells with defective telomerase.division, even in healthy people.
Rewinding the Clock for Aging Cells
Wednesday, March 3, 2010
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Aging Cells
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