Tag Archives: cellular machinery

Alzheimer’s and Parkinson’s update

Scientists have identified a potential therapeutic target to slow changes that lead to neurodegenerative disorders such as Parkinson”s and Alzheimer”s diseases.

Cell biologists pondering the death of neurons — brain cells — said that by eliminating one ingredient from the cellular machinery, they prolonged the life of neurons stressed by a pesticide chemical.

The researchers, from The University of Texas Health Science Center San Antonio, found that neurons lacking a substance called caspase-2 were better able to withstand pesticide-induced damage to energy centers known as mitochondria.

Alzheimer's disease

Alzheimer's disease

Caspase-2 appears to be a master switch that can trigger either cell death or survival depending on the amount of cellular damage, the team found. Neurons that lacked caspase-2 showed an increase in protective activities, including the efficient breakdown of obsolete or used proteins. This process, called autophagy, delays cell death.

“This research shows, for the first time, that in the absence of caspase-2 neurons increase autophagy to survive,” said study co-author Marisa Lopez-Cruzan, investigator in the cellular and structural biology department at the Health Science Center.

Evidence suggests that mitochondrial dysfunction plays an important role in neuronal death in conditions such as Parkinson”s disease, Alzheimer”s disease, amyotrophic lateral sclerosis (ALS, or Lou Gehrig”s disease) and Huntington”s disease.


“Identifying initiators in the cell death process is important for determining therapeutic approaches to provide the maximum protection of neurons during neurodegenerative conditions,” said senior author Brian Herman, Ph.D., vice president for research and professor of cellular and structural biology at the Health Science Center.

The team studied neurons from young adult mice. This was intended to model the early changes that take place in neurodegenerative diseases.

Dr. Lopez-Cruzan, director of Dr. Herman”s laboratory, came up with the idea that caspase-2 protects cells from mitochondrial stress. Meenakshi Tiwari, postdoctoral fellow, expanded upon the initial work and is first author of the paper.

The research is in the March 11 issue of the Journal of Biological Chemistry.

Potential drug for Alzheimer’s

A new discovery by UC Santa Barbara scientists has the potential for use in the early diagnosis and eventual treatment of plaque-related diseases such as Alzheimer’s disease and Type 2 diabetes.

The amyloid diseases are characterized by plaque that aggregates into toxic agents that interact with cellular machinery, explained Michael T. Bowers, lead author and professor in the Department of Chemistry and Biochemistry. Other amyloid diseases include Parkinson”s disease, Huntington”s disease, and atherosclerosis. Amyloid plaques are protein fibrils that, in the case of Alzheimer”s disease, develop prior to the appearance of symptoms.

“The systems we use are model systems, but the results are groundbreaking,” said Bowers.

Alzheimer’s disease

Alzheimer’s disease

He explained that his research provides the first examples of the conversion of randomly assembled aggregates of small peptides into ordered beta sheets that comprise fibrils. Fibrils are the final structural state of the aggregation process.

In the article, Bowers describes how understanding the fundamental forces that relate aggregation, shape, and biochemistry of soluble peptide aggregates is central to developing diagnostic and therapeutic strategies for amyloid diseases.

Bowers and his research team used a method called ion-mobility spectrometry-mass spectrometry (IMS-MS). This method enabled the team to deduce the peptide self-assembly method. They then examined a series of amyloid-forming peptides clipped from larger peptides or proteins associated with disease.


Bowers explained that IMS-MS has the potential to open new avenues for investigating the pathogenic mechanisms of amyloid diseases, their early diagnosis and eventual treatment.

The study has been published in the Nature Chemistry.