New method to reduce accumulation of damaging Huntington's disease protein
- Date:
- April 15, 2016
- Source:
- University of California - Irvine
- Summary:
- There may be a new way to change the damaging course of Huntington disease, researchers report. They have shown that reducing the aberrant accumulation of a particular form of the mutant Huntingtin protein corresponds to improvement in symptoms and neuroinflammation in HD mice.
- Share:
A study appearing April 14 in the journal Neuron suggests there may be a new way to change the damaging course of Huntington disease.
University of California, Irvine neurobiologists Leslie Thompson and Joseph Ochaba with the Departments of Neurobiology & Behavior and Psychiatry & Human Behavior and their colleagues from UCI and from Children's Hospital of Philadelphia have shown that reducing the aberrant accumulation of a particular form of the mutant Huntingtin protein corresponds to improvement in symptoms and neuroinflammation in HD mice.
They showed this by targeting and modulating levels of PIAS1 -- a protein implicated in cancer and other diseases -- which they found led to the reduction of the mutant Huntington protein. The work suggests that changing levels of the PIAS1 protein and targeting this pathway could have a benefit to disease.
There are no current treatments for HD, although Thompson's ongoing work with stem cell-based therapies are showing promise.
Story Source:
Materials provided by University of California - Irvine. Note: Content may be edited for style and length.
Journal Reference:
- Joseph Ochaba, Alex Mas Monteys, Jacqueline G. O’Rourke, Jack C. Reidling, Joan S. Steffan, Beverly L. Davidson, Leslie M. Thompson. PIAS1 Regulates Mutant Huntingtin Accumulation and Huntington’s Disease-Associated Phenotypes In Vivo. Neuron, 2016; DOI: 10.1016/j.neuron.2016.03.016
Cite This Page: