Presynaptic Protein Predicts Excitatory Synapse Formation
Labelled Neurons in a Drosophila melanogaster Brain. Credit: Timothy Mosca, Jefferson
Many neurological diseases are malfunctions of synapses, or the points of contact between neurons that allow senses and other information to pass from finger to brain. In the brain, there is a careful balance between the excitatory synapses that allow messages to pass, and the inhibitory synapses that dampen the signal. When that balance is off, the brain becomes unable to process information normally, leading to conditions like epilepsy.
Now researchers at Jefferson have discovered a molecule that may play a role in helping maintain the balance of excitatory and inhibitory neurons. The results were published in the journal eLife, a project of the Howard Hughes Medical Institute, the Wellcome Trust and the Max Planck Institute.
Timothy Mosca, Ph.D., Assistant Professor in the Department of Neuroscience at the Vickie and Jack Farber Institute for Neuroscience of Thomas Jefferson University, discovered that a molecule called LRP4 was important in creating excitatory synapses, the ones that keep a message passing from one neuron to the next. When the researchers knocked out the LRP4 gene in fruit flies, they saw a 40 percent loss of excitatory synaptic connections in the brain, but no such loss of inhibitory synapses, suggesting that the molecule was specific to one kind of synapse.
See also: rapid labeling of Fly neurons
The researchers used a new technology called expansion microscopy to get a better view of the fruit fly neurons. “In most cases, if you want to see very small things with better resolution, you get a better microscope,” says Mosca. “The other option is to make the small things bigger.” By infusing the neurons they were studying with the chemical in diapers that swells as it absorbs water, they were able to make the neurons and their synapses enlarged enough to see them more clearly.
See also: expanding structures to see them
“Most molecules involved in synapse biology are vital to both excitatory and inhibitory neurons,” says Mosca. “The idea that we now have a molecule that appears to be specific to excitatory synapses suggests there is probably a parallel molecule that exists that helps form inhibitory ones, that we just haven’t found yet.”
A better understanding of the unique biology of excitatory and inhibitory synapses may go a long way in helping researchers untangle the many diseases that are thought to be related to synapse dysfunction such as epilepsy, but also autism and schizophrenia.
Article reference: T.J. Mosca et al., “Presynaptic LRP4 Promotes Synapse Number and Function of Excitatory CNS Neurons,” eLife, 6:e27347, 2017.
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