Molecules may “anchor” memories in the brain
Nov. 21, 2006
Courtesy University of Utah
and World Science staff
These connections, called synapses, “are in a constant state of flux. They are exchanging molecules all the time,” said Paul Bressloff of the University of Utah in Salt Lake City.
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Deep inside the brain, a neuron prepares to transmit a signal to its target. This image won the U.S. National Science Foundation's Science & Engineering Visualization Challenge image competition last year. (Credit: Graham Johnson Medical Media). |
The research, he said, is also relevant to learning and Alzheimer’s disease. That illness is thought to involve, at least in part, a malfunction in protein movements in synapses.
Bresloff and a co-author detailed their work in the Nov. 22 issue of The Journal of Neuroscience. Both authors are mathematicians, not biologists. But Bressloff said he’s not worried about possible skepticism from scientists who may argue that it will take experiments, not mathematical theories, to prove his point.
“Theory can be a reality check [on] experiments just as much as the other way around,” wrote Bressloff, a member of the university’s Brain Institute, in an email.
On the subject that his study covers, he added, there’s already “an overwhelming amount of experimental data, much of which appears to be contradictory.”
Bressloff said the big debate on consciousness is, “can it be explained simply in terms of a bunch of nerve impulses in the brain? In my opinion, the answer has to be yes”—and his findings reinforce that. “If you change the pattern of nerve impulses, then that changes the memories, behavior and feelings. … What determines that pattern of nerve impulses is a mixture of stimuli we are receiving from the outside world and the strength of connections between nerve cells.”
The strength of these links determines who we are, he argued.
A synapse, the junction between nerve cells or neurons, has three parts: an end or “axon” of the transmitting cell; a microscopic gap between cells; and a mushroom-shaped “dendritic spine,” which is part of the receiving cell.
What we learn and remember is believed to be distributed across many synapses, Bressloff said. Some memories, such as a person’s face, may rely on just a few synapses; other memories may be distributed across many.
While a nerve cell has only one axon to transmit outgoing signals, it has many branch-like structures called dendrites. Each dendrite, in turn, branches into twig-like protrusions known as dendritic spines. A nerve cell may have 10,000 dendritic spines, each of which is part of a synapse. So the cell can get signals from that many other nerve cells.
Nerve cells fire electric impulses. When an impulse arrives at the synapse, it triggers the release of chemicals called neurotransmitters. These cross the synapse and attach or “bind” to proteins on the dendritic spine, called receptors. These help the signal continue on the other side.
A key neurotransmitter, glutamate, binds to proteins known as AMPA receptors, embedded in the dendritic spines on the receiving cells. These receptors are one of two receptor types known to play a crucial role in learning and memory, Bresloff said. The AMPA receptors, he added, are held in the membrane covering the cell by other molecules called scaffolding proteins.
Earlier research indicates learning and memory depend on the strength of synapses. Bressloff said a synapse’s strength depends not only on how much neurotransmitter the upstream cell sends, but on other factors, including the number of receptors like AMPA.
Bressloff studied how synapse strength relates to the number of AMPA receptors, which helps determine the strength of a transmitted current.
Individual receptors constantly are recycled or “trafficked” in and out of the synapse, he said. How can the ever-changing synapse help retain learning and memories? He created a mathematical simulation to describe receptor movements based on the idea that the receiving, mushroom-shaped dendritic spine has two compartments. One looks like the mushroom cap; it’s where scaffolding proteins pin receptors in place so they can receive glutamate’s chemical signal. The second compartment is like the mushroom’s stalk.
Bressloff used equations to describe how quickly receptors leave or enter a synapse by going between the “cap” and “stalk.” The equations suggested that the biggest factor in strengthening synapses was the scaffolding proteins. “You can’t just shove a bunch of new AMPA receptors to the surface because they will just go away again,” he said; “you need to keep them there.” What we remember and learn is in effect, he argued, anchored to nerve cells.
http://www.world-science.net/othernews/061121_memories.htm
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