Summary: A new study challenges the long-held belief that axons, brain cell extensions, are tube-like, revealing instead a “pearl-on-a-string” structure.
Using advanced freezing electron microscopy, researchers found these bead-like formations, termed “non-synaptic varicosities,” across mouse neurons. These structures may influence brain signaling by modulating ion flow and electrical signal speed. Changes in membrane stiffness, such as reduced cholesterol levels, alter the pearls’ size and signal transmission ability.
This discovery reshapes our understanding of neuron structure and opens doors for exploring its implications in neurodegenerative diseases. Future work will examine these formations in human brain tissues.
Key Facts:
- Axons exhibit “pearl-on-a-string” shapes, not constant cylindrical tubes.
- Removing cholesterol in axons reduces pearling and slows electrical signals.
- High-frequency electrical stimulation temporarily swells these pearl structures.
Source: Johns Hopkins Medicine
Biology textbooks may need a revision, say Johns Hopkins Medicine scientists, who present new evidence that an armlike structure of mammalian brain cells may be a different shape than scientists have assumed for more than a century.
Their study on mouse brain cells shows that the cells’ axons — the armlike structures that reach out and exchange information with other brain cells — are not the cylindrical tubes often pictured in books and on websites but more like pearls on a string.
A report on the findings is published online Dec. 2 in Nature Neuroscience.
“Understanding the structure of axons is important for understanding brain cell signaling,” says Shigeki Watanabe, Ph.D., associate professor of cell biology and neuroscience at the Johns Hopkins University School of Medicine. “Axons are the cables that connect our brain tissue, enabling learning, memory and other functions.”
Scientists have known that pearl-like structures in axons, referred to as axon beading, can develop in dying brain cells and in people with Parkinson’s and other neurodegenerative diseases due to the loss of membrane and skeletal integrity in neurons.
Under normal conditions, axons are thought to be shaped like tubes with a mostly constant diameter and occasional bubble-like structures (synaptic varicosities that hold globs of neurotransmitters, which enable signaling to other brain cells).
Watanabe had initially seen repeated axon pearling in the nervous system of worms and grew more curious about the structures after a discussion with Swiss scientist Graham Knott, Ph.D. A research team from Harvard University had published a study in 2012 that identified repeated “skeletal” components in axons, so the pair of researchers discussed experiments to get rid of the axon skeleton to see if the pearl structures disappear, says Watanabe.
Johns Hopkins graduate student and study first author Jacqueline Griswold tested the idea but found no effect on axon pearling.
Then, Watanabe and Griswold worked with theoretical biophysics colleague Padmini Rangamani, Ph.D., professor of pharmacology at University of California San Diego School of Medicine, to look more closely at axons’ physical properties.
To be able to see axons on brain cells (neurons), which are 100 times smaller than the width of a human hair, the scientists used high pressure freezing electron microscopy.
Like standard electron microscopy, which shoots beams of electrons at a cell to outline its structure, Watanabe and his team froze mouse neurons to preserve the structures’ shape.
“To see nanoscale structures with standard electron microscopy, we fix and dehydrate the tissues, but freezing them retains their shape — similar to freezing a grape rather than dehydrating it into a raisin,” says Watanabe.
The researchers studied three types of mouse neurons: ones grown in the lab, those taken from adult mice and those taken from mouse embryos. The neurons were nonmyelinated (they were without the myelin insulating cover that surrounds the axon).
The researchers found the bubbly, pear shape of axons among all of the tens of thousands of images taken of the tissue samples.
The scientists named the pearl-like structures in which the axon swells “non-synaptic varicosities.”
“These findings challenge a century of understanding about axon structure,” says Watanabe.
The scientists also used mathematical modeling to see if the axon membrane influenced the shape or presence of the pearl on a string structure. They found that simple mechanical models could be used to explain these structures very effectively.
Furthermore, experiments with the mathematical model and mouse brain samples showed that increasing the concentration of sugars in the solution around the axon or decreasing tension in the axonal membranes reduced the pearl structures’ size.
In another experiment, the scientists removed cholesterol from the neuron’s membrane to make it less stiff and more fluid-like. Under this condition, they found less pearling in both mathematical models and mouse neurons, along with reduced ability of the axon to transmit electrical signals.
“A wider space in the axons allows ions [chemical particles] to pass through more quickly and avoid traffic jams,” says Watanabe.
The scientists also applied high frequency electrical stimulation to the mouse neurons, which made pearled structures along axons swell, on average, 8% longer and 17% wider for at least 30 min after stimulation and increased the speed of electrical signals.
However, when cholesterol was removed from the membrane, the axon’s pearls lost their swollen state and had no change in the speed of electrical signals.
The research team plans to examine axonal “arms” in human brain tissue taken with permission from people having brain surgery and those who have died from neurodegenerative diseases.
This work formed the basis of a recently awarded Multiple Principal Investigator grant to Watanabe and Rangamani from the National Institute of Mental Health.
Funding: Funds for the research were provided by the Johns Hopkins University School of Medicine, the Marine Biological Laboratory Whitman Fellowship, the Chan Zuckerberg Initiative Collaborative Pair Grant and Supplement Award, the Brain Research Foundation Scientific Innovations Award, a Helis Foundation award, the National Institutes of Health (NS111133-01, NS105810-01A11, DA055668-01, 1RF1DA055668-01), the Air Force Office of Scientific Research (FA9550-18-1-0051), the Alfred P. Sloan Research Fellowship, a McKnight Foundation scholarship, a Klingenstein-Simons Fellowship Award in Neuroscience, a Vallee Foundation scholarship, the National Science Foundation and the Kavli Institutes at Johns Hopkins and UC San Diego.
Other researchers who conducted the study are Chintan Patel, Renee Pepper, Sumana Raychaudhuri, Quan Gan, Sarah Syed and Brady Maher from Johns Hopkins, Mayte Bonilla-Quintana, Christopher Lee, Cuncheng Zhu and Miriam Bell from the UC San Diego, Siyi Ma from the Marine Biology Laboratory, Mitsuo Suga and Yuuki Yamaguchi from JEOL in Tokyo, and Ronan Chéreau and U. Valentin Nägerl from the Université de Bordeaux in France.
About this neuroscience research news
Author: Vanessa Wasta
Source: Johns Hopkins Medicine
Contact: Vanessa Wasta – Johns Hopkins Medicine
Image: The image is credited to Quan Gan, Mitsuo Suga, Shigeki Watanabe
Original Research: Open access.
“Membrane mechanics dictate axonal pearls-on-a-string morphology and function” by Shigeki Watanabe et al. Nature Neuroscience
Abstract
Membrane mechanics dictate axonal pearls-on-a-string morphology and function
Axons are ultrathin membrane cables that are specialized for the conduction of action potentials. Although their diameter is variable along their length, how their morphology is determined is unclear.
Here, we demonstrate that unmyelinated axons of the mouse central nervous system have nonsynaptic, nanoscopic varicosities ~200 nm in diameter repeatedly along their length interspersed with a thin cable ~60 nm in diameter like pearls-on-a-string. In silico modeling suggests that this axon nanopearling can be explained by membrane mechanical properties.
Treatments disrupting membrane properties, such as hyper- or hypotonic solutions, cholesterol removal and nonmuscle myosin II inhibition, alter axon nanopearling, confirming the role of membrane mechanics in determining axon morphology.
Furthermore, neuronal activity modulates plasma membrane cholesterol concentration, leading to changes in axon nanopearls and causing slowing of action potential conduction velocity.
These data reveal that biophysical forces dictate axon morphology and function, and modulation of membrane mechanics likely underlies unmyelinated axonal plasticity.
