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Slowing neurodegeneration in Huntington’s

Article / Review by on December 18, 2011 – 8:28 pmNo Comments

Slowing neurodegeneration in Huntington’s
Increase in regulatory enzyme may offer protection

University of Tennessee "Diseases such as Huntington's, Parkinson's, and Alzheimer's disease have different causative factors, but they share common themes — such as aggregation of misfolded proteins — and a unifying end point, the degenerative loss of neurons," says Harvard Medical School Professor of Neurology Dimitri Krainc. In this image, transmission electron microscopy demonstrates the fibrillar nature of huntingtin aggregates./ Image courtesy C. Stanley, T. Perevozchikova, and V. BerthelierUniversity of Tennessee “Diseases such as Huntington’s, Parkinson’s, and Alzheimer’s disease have different causative factors, but they share common themes — such as aggregation of misfolded proteins — and a unifying end point, the degenerative loss of neurons,” says Harvard Medical School Professor of Neurology Dimitri Krainc. In this image, transmission electron microscopy demonstrates the fibrillar nature of huntingtin aggregates./ Image courtesy C. Stanley, T. Perevozchikova, and V. Berthelier

Treatment that increases brain levels of an important regulatory enzyme may slow the loss of brain cells that characterizes Huntington’s disease (HD) and other neurodegenerative disorders.  In a report receiving advance online publication in Nature Medicine, a Massachusetts General Hospital (MGH)-based research team reports that increased expression of Sirt1, one of a family of enzymes called sirtuins, in the brain of a mouse model of HD protected against neurodegeneration. They also identified a potential mechanism for this protective effect.

“Diseases such as Huntington’s, Parkinson’s, and Alzheimer’s disease have different causative factors, but they share common themes — such as aggregation of misfolded proteins — and a unifying end point, the degenerative loss of neurons,” says the study’s senior author Dimitri Krainc of the MassGeneral Institute for Neurodegenerative Disease (MGH-MIND) and Harvard Medical School, where he is an associate professor of neurology. “Pharmacological targeting of Sirt1 may provide an opportunity for therapeutic development in HD and, more generally, in the neurodegenerative disorders of aging.”

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, causing destruction of brain cells.  Symptoms of HD usually first appear in the middle years and worsen over the 10- to 30-year course of the disorder, leading to death from a variety of complications.  Sirt1 is an important regulator of the activity of proteins involved in many critical functions — including energy metabolism, inflammation, and stress tolerance — and recent studies have suggested it protects against the effects of several neurodegenerative diseases.

In experiments with a mouse model of HD, the researchers first showed that knocking out Sirt1 expression in the brain accelerated the appearance of HD-like pathology — such as aggregates of mutant huntingtin and increased cell damage in key areas of the brain.  In contrast, a strain of HD mice in which Sirt1 was overexpressed lived longer, with significantly less neurodegeneration and huntingtin aggregation, than did HD mice in which Sirt1 expression was unaltered.  Cellular experiments showed that Sirt1 overexpression directly protects neurons from the toxic effect of mutant huntingtin.

The MGH-MIND team also discovered a new target for Sirt1 activity in TORC1, a brain protein known to regulate several important neuronal genes, and found that the presence of mutant huntingtin interferes with the interaction between Sirt1 and TORC1, reducing expression of the regulated genes.  In the same issue of Nature Medicine, a research team based at Johns Hopkins School of Medicine reports similar neuroprotective effects for Sirt1.  Co-authored by members of Krainc’s team, the Hopkins study demonstrated that mutant huntingtin inhibits the activity of Sirt1, leading to deregulation of multiple Sirt1 targets, in two additional HD mouse models.

“Development of therapeutic agents for neurodegenerative diseases requires an in-depth understanding of the mechanisms that link the underlying biology with the resulting neuronal dysfunction,” says Krainc. “Developing and testing Sirt1 activators that protect against disorders like HD will require accurate information on Sirt1 activity in the normal and diseased brain.  We hope our studies can contribute valuable data to that effort, which will require collaborations with NIH, with industry, and with foundations such as the Cure Huntington’s Disease Initiative, one of the supporters of this study.”

Additional supporters of the investigation are the National Institutes of Health, the Hereditary Disease Foundation, and the Glenn Foundation for Medical Research.

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About Harvard Medical School (HMS)

Driving Change. Building Momentum. Making History. 

Since 1872, Harvard Medical School has been the incubator of bold ideas—a place where extraordinary people advance education, science and health care with unrelenting passion.

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About Harvard School of Public Health (HSPH)

Harvard School of Public Health is dedicated to advancing the public’s health through learning, discovery and communication. More than 400 faculty members are engaged in teaching and training the 1,000-plus student body in a broad spectrum of disciplines crucial to the health and well being of individuals and populations around the world. Programs and projects range from the molecular biology of AIDS vaccines to the epidemiology of cancer; from risk analysis to violence prevention; from maternal and children’s health to quality of care measurement; from health care management to international health and human rights.

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*  The above story is adapted from materials provided by Harvard University

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