A new study has identified a potential strategy for removing the abnormal protein that causes Huntington’s disease from brain cells, which could slow the progression of the devastating neurological disorder.
Modification of mutant huntingtin protein increases its clearance from brain cells
Findings could lead to new approach to treating Huntington's, other neurodegenerative disorders
A new study has identified a potential strategy for removing the abnormal protein that causes Huntington’s disease (HD) from brain cells, which could slow the progression of the devastating neurological disorder. In the April 3 issue of Cell, a team of researchers from the MassGeneral Institute for Neurodegenerative Disease (MGH-MIND) describes how an alteration to the mutated form of the huntingtin protein appears to accelerate its breakdown and removal through normal cellular processes.
"Using Huntington’s disease as a model, we identified a mechanism whereby modification of the disease-causing protein itself facilitates the cell’s own method of digesting and recycling the mutant protein," says Dimitri Krainc, MD, PhD, of MGH-MIND and the Massachusetts General Hospital (MGH) Department of Neurology. "This enhanced clearance improved neuronal functioning and prevented neurodegeneration in cellular and animal models."
HD is an inherited disorder caused by a mutation in the gene for a protein called huntingtin. Deposits of the abnormal protein accumulate within the brain, leading to the degeneration and death of brain cells. Symptoms of HD, which usually begin to appear in the middle years, include uncontrolled movements, erratic emotions and problems with thinking and memory. Symptoms worsen over the 10- to 30-year course of the disorder, until patients die from a variety of complications.
Studies of mutant huntingtin by MGH-MIND researchers and their collaborators suggested a possible connection with a process of protein modification called acetylation, in which enzymes add a molecule called an acetyl group to the amino acid lysine. While the acetylation of histones, proteins involved in gene regulation, has been known for 40 years, it only recently has been discovered that other proteins are also acetylated, suggesting that the process has a broader array of functions. After discovering that mutant huntingtin interacts with known acetylation-inducing enzymes, the MGH-MIND team set out to investigate whether acetylation has a role in the disease.
After first confirming that mutant huntingtin is acetylated by a specific group of enzymes, the researchers showed that mutant protein made resistant to acetylation formed significantly larger deposits in mouse brains and was more toxic than acetylation-sensitive huntingtin. In a C. elegans roundworm model of HD, acetylation of mutant huntingtin significantly reduced neurodegeneration. Other experiments indicated that acetylation accelerates clearance of the mutant protein from cells by means of autophagy - a natural cellular process for digesting and removing unnecessary or abnormal proteins and other components.
A key observation was that acetylation, while increasing the removal of mutant huntingtin, had little effect on the normal version of the protein. "One of the major challenges of research into neurodegenerative disorders like Huntington’s, Alzheimer’s and Parkinson’s diseases - all of which involve accumulation of proteins within the brain - has been how to activate degradation machinery that only removes the disease-causing proteins and leaves normal proteins untouched," Krainc explains.
"Among several candidate HD drugs currently in development are some that increase acetylation, but we need to identify more specific versions of these drugs that target only the mutant protein and don’t affect other cellular pathways. In addition to huntingtin, we are examining whether acetylation of other disease-associated proteins affects their degradation and are interested in the detailed molecular mechanisms responsible for the recognition of acetylated proteins by the autophagic degradation machinery," he adds. Krainc is an associate professor of Neurology at Harvard Medical School.
Co-lead authors of the Cell paper are Hyunkyung Jeong, MS, and Florian Then, MD, MGH-MIND. Additional co-authors are Joseph Mazzulli, PhD, and Libin Cui, PhD, MGH-MIND; Anne Hart, PhD, and Cindy Voisine, PhD, MGH Center for Cancer Research; Thomas Melia, PhD, Yale University; Jeffrey Savas and Naoko Tanese, PhD, New York University; Paolo Paganetti, PhD, Novartis Pharmaceuticals; and Ai Yamamoto, PhD, Columbia College of Physicians and Surgeons. The study was supported by grants from the National Institutes of Health.
Massachusetts General Hospital, established in 1811, is the original and largest teaching hospital of Harvard Medical School. The MGH conducts the largest hospital-based research program in the United States, with an annual research budget of more than $500 million and major research centers in AIDS, cardiovascular research, cancer, computational and integrative biology, cutaneous biology, human genetics, medical imaging, neurodegenerative disorders, regenerative medicine, systems biology, transplantation biology and photomedicine.
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