Muscle Can Turn A Deaf Ear To Nerve, Study Finds

January 17, 1997

St. Louis, MO -- Jan. 17, 1997 -- When two or more nerves vie to be the only life-long partner of a muscle fiber, the muscle appears to play the decisive role, according to a research article in today's issue of Science. The fiber strengthens its relationship with one suitor, ignoring the others, which soon depart.

"The nerve cells try desperately to talk to the muscle, but the muscle has its fingers in its ears," says Jeff Lichtman, M.D., Ph.D., professor of anatomy and neurobiology at Washington University School of Medicine in St. Louis.

If cells in the central nervous system behave the same way, the finding could help explain how memories are soldered into the brain, preserving facts and faces for many decades.

Howard Colman, an M.D./Ph.D. student who worked in Lichtman's lab, is lead author of the paper, which is highlighted in the "Perspectives" section of the journal.

Neurons communicate through axons -- long "wires" that reach out to other neurons or muscle fibers during development and stay connected for life unless they're pruned away. The axons branch at their tips, where they join to target cells at junctions called synapses. Because synapses in the brain are so inaccessible < though there are trillions of them -- the more easily reached neuromuscular junction has become the standard synapse for study.

A massive pruning of surplus axons from muscle fibers occurs during the first four weeks of a mouse's life -- and in young humans. So each fiber ends up with only one axon. But how this elimination occurs has been one of the intractable problems in neuroscience.

In the 1980s, Lichtman and colleagues invented a way to look repeatedly at the same synapses in living mice. "You can literally see neurons that are co-innervating the same target cell," he says. "And you can watch the connections disappear over time."

Nerves activate muscles by releasing packets containing a chemical called acetylcholine at synapses. Muscle fibers detect this message with membrane proteins called acetylcholine receptors, which cluster directly under nerve terminals. Receptor activation sparks a chain of events that makes the muscle contract.

Studies in Lichtman's lab with a snake toxin that inactivates acetylcholine receptors led to a surprising finding, described in Nature in 1994. Before this time, scientists thought that two axons on the same fiber might act like battering rams, competing with each other for growth factors and space. "But we found that the receptors on the postsynaptic membrane disappeared before the nerve terminal withdrew," Lichtman says. "So the muscle cell is not just a passive witness -- it seems to know which synapses are going to be removed before elimination actually occurs."

These structural studies made Lichtman wonder whether muscle fibers rebuff already dying axons, leaving only healthy ones in place, or whether a muscle fiber decides among healthy axons which one will remain. "We had nothing to prove that the change in the muscle fiber occurs before any change in the nerve terminal," he says. "So we wanted to find out if healthy axons are still trying to communicate with muscles at the time acetylcholine receptors disappear."

Colman and Lichtman addressed this question with electrophysiologic experiments on living trapezius muscle, which they removed from the neck of newborn mice. The muscle remained attached to the two nerve branches that control it in the body.

As axon pruning proceeded, Colman periodically stimulated each nerve branch and recorded the resulting electrical responses of individual muscle fibers. He studied only those fibers that were innervated by axons from each nerve. To better interpret the results, Lichtman invented a way to display the electrical recordings as color-coded 3-D images.

One part of the study measured the relative strengths of the chemical messages from pairs of competing axons -- the number of packets of acetylcholine released. In the first few days of life, the two axons in a pair tended to have similar strengths. But the strengths diverged as the days went by. When the mice were nine days old, for example, the majority of the remaining pairs had one axon that responded to stimulation by sending more than four times as many acetylcholine packets to a fiber as the other axon. "So the loser does not disappear suddenly < the strength of one input gets stronger while the other gets weaker," Lichtman says. "And we found that the stronger one wins."

Another part of the study focused on the effectiveness of the acetylcholine packets. By ranking responses to each axon, the researchers were able to see that, in many doubly innervated fibers, packets from the losing axon evoked weaker responses in the muscle than those from the stronger one, even though they contained the same amount of acetylcholine. It was as if the muscle was slighting a boring suitor in favor of a more interesting one.

"Our data, combined with other studies from our lab, support the idea that acetylcholine receptors are disappearing under the losing but otherwise healthy axon," Lichtman says.

The work suggests that synapse elimination may be a step-wise process. As a newborn animal learns to use its muscles to move around, an individual fiber will receive different signals from each of the axons that reach it. The signals may differ slightly in strength, or one axon may fire more often than the other. "So the muscle fiber may decide it likes one axon better than another and may start pulling receptors out from under the axon it doesn't like," Colman says. "That magnifies the small differences between the two axons, which rapidly come to differ more and more. Eventually, the losing axon takes the hint and disappears. So experience leads to axon elimination."

Although this process continues during the first four weeks of a mouse's life, the contest on any one fiber is over in a couple of days. "So that's an interesting analogy to learning and memory, where you have synaptic changes over a short period of time that lead to a permanent alteration in brain circuitry,"! ! Lichtman says.

Experiments by the paper's other author, former postdoc Junichi Nabekura, M.D., showed that synaptic elimination also can occur in adult animals by this same process. Nabekura made electrophysiologic measurements from fibers of injured muscles that were re-establishing connections with nerves. During the transition to single-axon innervation, signals from the losing axon had less and less effect on the muscle. "We concluded that the process of synapse elimination at the neuromuscular junction of adult animals is similar to that seen during development," Colman says. "So it's possible it also could occur in the adult brain."

No one knows how the brain preserves memories for long periods of time, Lichtman stresses. "But the idea that learning involves loss of connections requires the circuitry for associating any objects you might ever see to be in your brain from birth," he says. "Making a logical connection between a face and a name, for example, would involve preserving and strengthening synaptic connections between certain neurons while eliminating those between others. Our study links the large body of work that shows that experience modifies synaptic strength to a structural mechanism that permanently disconnects some axons and preserves others. If target cells in the brain could modify their connections in the same way, that would be an effective way for experience to permanently change the circuitry of the brain."
Colman H, Nabekura J, Lichtman JW. Alterations in synaptic strength preceding axon withdrawal. Science, 275, 356-361, 1997.

A graphic is available. Call 314-286-0119. To preview, go to:

Funding from the National Institute of Neurological Disorders and Stroke at the National Institutes of Health and from the Muscular Dystrophy Association supported this research.

Washington University School of Medicine

Related Brain Articles from Brightsurf:

Glioblastoma nanomedicine crosses into brain in mice, eradicates recurring brain cancer
A new synthetic protein nanoparticle capable of slipping past the nearly impermeable blood-brain barrier in mice could deliver cancer-killing drugs directly to malignant brain tumors, new research from the University of Michigan shows.

Children with asymptomatic brain bleeds as newborns show normal brain development at age 2
A study by UNC researchers finds that neurodevelopmental scores and gray matter volumes at age two years did not differ between children who had MRI-confirmed asymptomatic subdural hemorrhages when they were neonates, compared to children with no history of subdural hemorrhage.

New model of human brain 'conversations' could inform research on brain disease, cognition
A team of Indiana University neuroscientists has built a new model of human brain networks that sheds light on how the brain functions.

Human brain size gene triggers bigger brain in monkeys
Dresden and Japanese researchers show that a human-specific gene causes a larger neocortex in the common marmoset, a non-human primate.

Unique insight into development of the human brain: Model of the early embryonic brain
Stem cell researchers from the University of Copenhagen have designed a model of an early embryonic brain.

An optical brain-to-brain interface supports information exchange for locomotion control
Chinese researchers established an optical BtBI that supports rapid information transmission for precise locomotion control, thus providing a proof-of-principle demonstration of fast BtBI for real-time behavioral control.

Transplanting human nerve cells into a mouse brain reveals how they wire into brain circuits
A team of researchers led by Pierre Vanderhaeghen and Vincent Bonin (VIB-KU Leuven, Université libre de Bruxelles and NERF) showed how human nerve cells can develop at their own pace, and form highly precise connections with the surrounding mouse brain cells.

Brain scans reveal how the human brain compensates when one hemisphere is removed
Researchers studying six adults who had one of their brain hemispheres removed during childhood to reduce epileptic seizures found that the remaining half of the brain formed unusually strong connections between different functional brain networks, which potentially help the body to function as if the brain were intact.

Alcohol byproduct contributes to brain chemistry changes in specific brain regions
Study of mouse models provides clear implications for new targets to treat alcohol use disorder and fetal alcohol syndrome.

Scientists predict the areas of the brain to stimulate transitions between different brain states
Using a computer model of the brain, Gustavo Deco, director of the Center for Brain and Cognition, and Josephine Cruzat, a member of his team, together with a group of international collaborators, have developed an innovative method published in Proceedings of the National Academy of Sciences on Sept.

Read More: Brain News and Brain Current Events is a participant in the Amazon Services LLC Associates Program, an affiliate advertising program designed to provide a means for sites to earn advertising fees by advertising and linking to