Turning on the switch for plasticity in the human brain


Scientists describe how glutamate signals are transmitted across synapses to turn on the switch for synapatic plasticity, the ability of synapses to strengthen or weaken over time in response to increases or decreases in their activity.

Shigeki Watanabe of Johns Hopkins University School of Medicine, a familiar face at the Marine Biological Laboratory (MBL) as a faculty member and researcher, is hot on the trail of describing how glutamate signaling works in the brain to enable neuronal communication. In a paper last fall, Watanabe (along with several MBL Neurobiology course students) described how glutamate is released from neural synapses after the neuron fires. And today, Watanabe published a follow-up study in Nature Communications.

«With this paper, we uncover how signals are transmitted across synapses to turn on the switch for plasticity,» Watanabe says. «We demonstrate that glutamate is first released near AMPA-type glutamate receptors, to relay the signal from one neuron to the next, and then near NMDA-type receptors immediately after the first signal to activate the switch for synaptic plasticity.»

This new study was also partly conducted in the MBL Neurobiology course, where Watanabe is a faculty member. «It began in 2018 with (course students) Raul Ramos and Hanieh Falahati, and then we followed up in 2019 with Stephen Alexander Lee and Christine Prater. Shuo Li, the first author, was my teaching assistant for the Neurobiology course for both years,» Watanabe says. He will be returning to the MBL this summer to teach in the course — and discover more.


Story Source:
Materials provided by Marine Biological Laboratory. Original written by Diana Kenney. Note: Content may be edited for style and length.


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