From: Colorado State University
By Anne Manning
June 7, 2022 -- As
you’re reading this sentence, the cells in your brain, called neurons, are
sending rapid-fire electrical signals between each other, transmitting
information. They’re doing so via tiny, specialized junctions between them
called synapses.
There are many
different types of synapses that form between neurons, including “excitatory”
or “inhibitory,” and the exact mechanisms by which these structures are
generated remain unclear to scientists. A Colorado State University
biochemistry lab has uncovered a major insight into this question by showing
that the types of chemicals released from synapses ultimately guide which kinds
of synapses form between neurons.
Soham Chanda, assistant
professor in the Department of Biochemistry and Molecular Biology, led
the study published in Nature Communications that
demonstrates the possibility of changing the identity of synapses between
neurons, both in vitro and in vivo, through
enzymatic means. The other senior scientists who contributed to the project
were Thomas Südhof of Stanford University and Matthew Xu-Friedman of the
University at Buffalo.
In the lab, Chanda and
colleagues were able to make synapses changes between excitatory and inhibitory
types, using only enzymes, by making the neurons express just a few genes that
induced a cascade of changes in the synapses’ machinery. Such a breakthrough
could have major implications for treating brain diseases that are caused by
malfunctions in synaptic information processing and exchange.
“We know very little
about how the human brain functions, and at the center of it, we need to
understand how neurons communicate with each other,” Chanda said.
“Understanding the fundamental mechanisms of synapse formation and maintenance
has tremendous implications in understanding brain disorders.”
Their results show that
the cell-adhesion proteins expressed in the synaptic junction area are not the
only purveyors of the synapses’ function, as some have thought; rather,
chemicals called neurotransmitters that are released from the presynaptic site
(where the information is coming from) also seem to play a major role in
controlling which types of synapses form, and where.
The CSU team used stem
cell-derived human neurons to demonstrate their ability to produce certain
types of synaptic connections by controlled release of specific
neurotransmitters. Collaborators at the University at Buffalo showed the same
phenomenon in live mouse brains.
“Synapses need lots of
other machinery; the neurons took care of all that and turned excitatory
synapses into inhibitory ones – a fundamental change in their identity,”
Xu-Friedman said.
Chanda is fascinated by
neurons, “because no other cell type in the human body has the same level of
functional complexity that is tied so closely to their shape and structure.”
The students who
performed the majority of the experiments were co-authors Scott Burlingham and
Lindsay Peterkin at CSU, and Nicole Wong at the University at Buffalo.
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