The Ice Bucket Challenge campaign was part of an outstanding effort to raise awareness of ALS. But what made much less of a splash in the media is what researchers are doing to tackle the issue. At the University of Arizona, researchers have identified a molecular defect in motor neurons that may help explain the mechanisms underlying ALS, or Lou Gehrig's Disease.
Relatively little is known about exactly how and why ALS/MND occurs. In a rare discovery, a clear molecular defect has been found at the junctions between neurons and muscles, which may provide greater insight into the fundamental mechanisms of ALS, according to a new study by Daniela Zarnescu, Associate Professor in the University of Arizona's Department of Molecular and Cellular Biology, and graduate , a graduate student in the UA's Neuroscience Graduate Interdisciplinary Program. The paper was published in the November 26, 2014 edition of Journal of Neuroscience.
In healthy people, motor neurons make contact with muscle fibers at neuromuscular junctions, which allows for appropriate control of movement and other critical functions. In ALS patients, motor neurons die, preventing these connections from occurring. To study ALS, Zarnescu and Coyne use the fruit fly Drosophila melanogaster model, which enables them to more easily pinpoint exactly when and where the connections fail.
In microscope images of fruit fly and human neurons, proteins can be observed in motor neuron cell bodies. Compared to healthy neurons, the ALS neurons clearly show accumulations of the proteins. "When you tell people that you use the fruit fly as a model of human disease, you get some funny looks," Zarnescu said. "But using simplistic models can help you uncover what's really important in the context of the disease."
Zarnescu and Coyne found that TDP-43 regulates the creation and transport of another protein called Futsch at the neuromuscular junction. In the ALS model, TDP-43 prevents Futsch from making it to the neuromuscular junction, which results in a faulty connection.
"Alyssa discovered that this particular molecule is not regulated properly. It's not made in the right place or in the right amount," Zarnescu said. "Instead of being transported to the neuromuslcular junction, it stays in the body of the cell and can't maintain the stability of the connection." The researchers then wanted to determine if increasing the amount of Futsch protein would help repair the poor connection. Astoundingly, overexpressing Futsch in motor neurons had the effect of increasing the stability of the connection, increasing the lifespan of motor neurons and restoring motor function in the ALS fruit flies.
Zarnescu and Coyne then collaborated with researchers at the Barrow Neurological Institute in Phoenix to examine cells from the spinal cords of human ALS patients. The team looked at a protein called MAP1B, which is the mammalian version of the Futsch protein. Remarkably, the localization of MAP1B was altered in a very similar manner to the Futsch protein in fruit flies. The similarities suggest comparable defects in both human and fruit fly models of ALS.
"This highlights the importance of studying human disease in simple models," Zarnescu said. "These models are extremely powerful, and predictive of defects that occur in human patients." According to Zarnescu and Coyne, the findings represent a major step forward in understanding and eventually treating the disease. "This study is among the first to highlight such a clear molecular defect at synaptic connections in ALS," Zarnescu said. "We don't yet know exactly what is going on in ALS, but this discovery provides a possible explanation."
Information Contributed by Raymond Sanchez