image: From left, this picture shows SRI Professor Xiang-Lei Yang, SRI researcher Ge Bai and Salk Professor Sam Pfaff. view more
Credit: Salk Institute
LA JOLLA--Scientists have unraveled how mutant molecules damage the nervous system of people with Charcot-Marie-Tooth (CMT) disease, a group of disorders that hinder people's ability to move and feel sensation in their hands and feet, according to a paper published October 21, 2015 in Nature.
In laboratory testing, the researchers were able to improve symptoms of the disease in mice, raising hopes that they may have found an avenue for treating people with CMT.
The research, a collaboration between scientists from the Salk Institute and The Scripps Research Institute (TSRI), offers promising targets for developing new drugs for the disease. The findings may offer clues to understanding and treating other neurodegenerative disorders, including other forms of CMT.
"This solves a long-running mystery of how a gene mutation damages the neurons that carry information from the spinal cord to our muscles, resulting in a range of sensory and movement problems," says Samuel Pfaff, a neuroscience professor at the Salk Institute and one of the senior authors on the paper with Xiang-Lei Yang, a professor at TSRI. "It's an exciting finding, as we were able in experiments to reverse the symptoms of the disease by targeting the activity of these proteins."
CMT is a group of hereditary disorders that affects about 1 in every 2,500 people in the United States, making it one of the most common inherited neurological diseases. While different forms of the disease vary in their symptoms and underlying genetic causes, the common thread is that CMT damages the nerves in a person's arms and legs.
Symptoms of the disease, which typically appear in adolescence or early adulthood, include muscle weakness and decreased muscle size, loss of sensation and deformities in the feet and legs. The symptoms typically first appear in the lower extremities, but eventually may move into the hands.
It was known from early work from the Yang lab that one form of the disorder was caused by a gene mutation that resulted in a misshapen form of an enzyme known as GlyRS that serves many roles in cells, but how this resulted in neural damage remained a mystery.
The Salk and TSRI scientists used a range of neuro-genetic, gene therapy, biochemical and structural biology research techniques to discover that the mutant GlyRS enzyme blocked molecular signals important for maintaining the health of motor neurons, the cells that carry messages from the brain to the muscles of the extremities. One surprise was that the GlyRS enzyme, which was commonly thought to remain inside neurons, was actually found outside the neurons. That is where it blocked a protein known as VEGF from connecting with a molecular sensor, named Nrp1, which is found on the surface of the neurons.
"Normally, these molecular messages essentially tell the neurons 'you're healthy,' stimulating them to remain robust and active," says Yang. "By blocking this message, the mutant GlyRS enzyme causes the motor neurons to go into decline and even die, which breaks the connection between the brain and the muscles in the limbs."
Having identified the mechanism by which the gene mutation leads to neuropathy, the researchers tried amplifying the "health" signal to see if they could override the blockade of the mutant GlyRS molecules. When they turned up the volume on the signal, using gene therapy techniques to increase the production of the signaling molecule, the mice with CMT regained muscle strength and their ability to walk improved significantly.
The findings suggest a possible avenue for developing new therapies for CMT by either dampening the activity of the mutant GlyRS enzymes or amplifying the competing signal that promotes the health of the motor neurons.
More broadly, the research suggests a new framework for exploring how the mutated proteins interfere with normal processes for neuron survival in other neurodegenerative diseases.
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Other authors on the paper were Weiwei He, Ge Bai, Huihao Zhou, Na Wei, Nicholas M. White, Janelle Lauer, Huaqing Liu, Yi Shi, Calin Dan Dumitru, Karen Lettieri, Veronica Shubayev, Albena Jordanova, Velina Guergueltcheva, Patrick R. Griffin and Robert W. Burgess.
The research was supported by the National Institutes of Health, National Foundation for Cancer Research, the Marshall Heritage Foundation, the Sol Goldman Trust and aTyr Pharma.
About Salk
The Salk Institute for Biological Studies is one of the world's preeminent basic research institutions, where internationally renowned faculty probes fundamental life science questions in a unique, collaborative and creative environment. Focused both on discovery and on mentoring future generations of researchers, Salk scientists make groundbreaking contributions to our understanding of cancer, aging, Alzheimer's, diabetes and infectious diseases by studying neuroscience, genetics, cell and plant biology, and related disciplines. Faculty achievements have been recognized with numerous honors, including Nobel Prizes and memberships in the National Academy of Sciences. Founded in 1960 by polio vaccine pioneer Jonas Salk, MD, the Institute is an independent nonprofit organization and architectural landmark.
About The Scripps Research Institute
The Scripps Research Institute (TSRI) is one of the world's largest independent, not-for-profit organizations focusing on research in the biomedical sciences. TSRI is internationally recognized for its contributions to science and health, including its role in laying the foundation for new treatments for cancer, rheumatoid arthritis, hemophilia, and other diseases. An institution that evolved from the Scripps Metabolic Clinic founded by philanthropist Ellen Browning Scripps in 1924, the institute now employs about 2,700 people on its campuses in La Jolla, CA, and Jupiter, FL, where its renowned scientists--including two Nobel laureates--work toward their next discoveries. The institute's graduate program, which awards PhD degrees in biology and chemistry, ranks among the top ten of its kind in the nation. For more information, see http://www.scripps.edu.
Journal
Nature