Single enzyme gains the upper hand in two types of dementia
Gladstone Institutes News Jan 30, 2017
Scientists discover an enzyme that that could be targeted to treat both AlzheimerÂs disease and frontotemporal dementia.
Scientists at the Gladstone Institutes scored a rare two–for–one gain by discovering an enzyme that controls the levels of a protein implicated in both AlzheimerÂs disease and frontotemporal dementia.
ÂFor some time, we have known that low levels of the protein progranulin are associated with these two forms of dementia and that increasing levels improves deficit in animal models of the two diseases, said Steven Finkbeiner, MD, PhD, a senior investigator at Gladstone. ÂBut how could we use that as a possible therapy? ThatÂs what is exciting about our latest results.Â
In a new study published in the Journal of Biological Chemistry, FinkbeinerÂs team looked closely at progranulin, which is secreted from cells and controls inflammation. Having only one copy of the gene for progranulin causes frontotemporal dementia, the most common form of dementia in people under age 65, while having mutations in the progranulin gene is a risk factor for developing AlzheimerÂs disease. Both conditions result in lower levels of progranulin in the brain.
ÂWe wanted to know what might regulate the levels of progranulin, said Amanda Mason, a former PhD student in FinkbeinerÂs lab and lead author on the study. ÂMany processes in biology are controlled by adding or removing a small chemical group called phosphate, so we started there.Â
The team used a genetic method to look for enzymes that help to remove phosphate groups in mice. Surprisingly, among the enzymes they found, one – serine/threonine protein kinase 1, or Ripk1 for short – increased the levels of progranulin inside and outside of the cells. The real bonus was that Ripk1 worked in mouse models of both AlzheimerÂs disease and frontotemporal dementia. Interestingly, the effect did not depend on the removal of the phosphate groups from progranulin, which implies that the effect comes about through a nonenzymatic mechanism.
ÂThis is an exciting finding, said Finkbeiner. ÂAlzheimerÂs disease was discovered over 100 years ago, and we have essentially no drugs to treat it. To find a possible new way to treat one disease is wonderful. To find a way that might treat two diseases is amazing.Â
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Scientists at the Gladstone Institutes scored a rare two–for–one gain by discovering an enzyme that controls the levels of a protein implicated in both AlzheimerÂs disease and frontotemporal dementia.
ÂFor some time, we have known that low levels of the protein progranulin are associated with these two forms of dementia and that increasing levels improves deficit in animal models of the two diseases, said Steven Finkbeiner, MD, PhD, a senior investigator at Gladstone. ÂBut how could we use that as a possible therapy? ThatÂs what is exciting about our latest results.Â
In a new study published in the Journal of Biological Chemistry, FinkbeinerÂs team looked closely at progranulin, which is secreted from cells and controls inflammation. Having only one copy of the gene for progranulin causes frontotemporal dementia, the most common form of dementia in people under age 65, while having mutations in the progranulin gene is a risk factor for developing AlzheimerÂs disease. Both conditions result in lower levels of progranulin in the brain.
ÂWe wanted to know what might regulate the levels of progranulin, said Amanda Mason, a former PhD student in FinkbeinerÂs lab and lead author on the study. ÂMany processes in biology are controlled by adding or removing a small chemical group called phosphate, so we started there.Â
The team used a genetic method to look for enzymes that help to remove phosphate groups in mice. Surprisingly, among the enzymes they found, one – serine/threonine protein kinase 1, or Ripk1 for short – increased the levels of progranulin inside and outside of the cells. The real bonus was that Ripk1 worked in mouse models of both AlzheimerÂs disease and frontotemporal dementia. Interestingly, the effect did not depend on the removal of the phosphate groups from progranulin, which implies that the effect comes about through a nonenzymatic mechanism.
ÂThis is an exciting finding, said Finkbeiner. ÂAlzheimerÂs disease was discovered over 100 years ago, and we have essentially no drugs to treat it. To find a possible new way to treat one disease is wonderful. To find a way that might treat two diseases is amazing.Â
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