Battens Disease

Phospholipids, Endosomes and Brain Function in Battens Disease
2006 Seed Grant
Glyn Dawson, Ph.D.
The University of Chicago

Dr. Dawson’s laboratory focuses on Batten disease, a neurodegenerative disease that results in mental retardation and premature death. Batten disease is a lysosomal storage disease in which undigested proteins accumulate inside membrane-bounded organelles in cells called lysosomes. Defects in lysosomal enzymes, that ordinarily breakdown discarded materials, cause a build up of proteins leading to severe pathological consequences (neuronal death). Batten disease is autosomal recessive. Normal adults can be carriers for Batten disease. If both parents carry one defective gene there isa one out of four chance that the fetus will be severely retarded. DNA-based testing can be done on amniotic fluid to determine the mental health of the fetus. Unfortunately, if the test is positive, the parents are now faced with the difficult decision of whether to bring the baby to term. Any intervention that improves the prognosis of this disease would be a welcomed development.

Batten disease involves at least nine different genes and more than 100 different mutations in each gene. This complexity makes Batten disease difficult to cure. Dr. Dawson is trying to reduce the source of accumulated proteins in lysosomes through drug therapy to slow down the disease. His laboratory has been focusing on one mutated enzyme in the disease, palmitoyl protein thioesterase (PPT1). Dr. Dawson’s team synthesized a drug DAPl to block the production of the undigestible proteins. DAPl was not as effective as they had hoped but it did inhibit PPTl and enabled them to create a model for Batten disease in isolated cells. Serendipitously, they found DAPl to be an anti-cancer drug because of its ability to promote cell death. DAPl helped chemotherapeutic drugs such as adriamycin and tamoxifan kill tumor cells. Dr. Dawson is thinking to the future and is working hard to develop a second generation of drugs that will decrease cell death and combat Batten disease.

Other Grants

José Manuel Baizabal Carballo, Ph.D., Indiana University Bloomington
Heterochromatin Mechanisms of Cortical Expansion
Neurodevelopmental disorders, such as autism and schizophrenia, are frequently associated with mutations in genes that encode chromatin-modifying enzymes. A subset of these mutations is thought to disrupt compacted chromatin (heterochromatin),…
Jessica L. Bolton, Ph.D., Georgia State University
Chemogenetic Tools in Microglia as a Novel Therapeutic Approach for Brain Disorders
All humans are born with a unique combination of genes, which contribute greatly to who we are. However, early-life experiences such as trauma or hardship, particularly during the first few…
Junyue Cao, Ph.D., The Rockefeller University
Elucidate the Molecular and Cellular Targets of Caloric Restriction in Rejuvenating Aged Mammalian Brain
As we age, the brain’s ability to function declines, increasing the risk of cognitive impairments and neurological diseases like Alzheimer’s and Parkinson’s. Our research investigates how caloric restriction (CR), a…
Vasileios Christopoulos, Ph.D., University of Southern California
Understanding the Mechanisms of Micturition in the Brain and Spinal Cord
This research aims to better understand how the brain and spinal cord work together to control urination, a process known as micturition. In healthy individuals, this process is carefully coordinated…