(Medical Xpress) -- Researchers at the National Institutes of Health have discovered in mice a molecular trigger that initiates myelination, the process by which brain cell networks are reinforced with an insulating material called myelin that speeds their ability to transmit messages.
The researchers showed that an electrical signal passing through a brain cell (neuron) results in the brain cell releasing the molecule glutamate. Glutamate, in turn, triggers another type of brain cell, called an oligodendrocyte, to form a point of contact with the neuron. Signals transmitted through this contact point stimulate the oligodendrocyte to make myelin protein and begin the process of myelination. In this process, the oligodendrocyte wraps myelin around axons the long, cable-like projections that extend from each neuron. The myelination process is analogous to wrapping electrical tape around bare wires.
Electrical signals transmitted from one neuron to the next are a basic form of communication in the brain. The myelin layers that oligodendrocytes wrap around neurons boost these signals so that they travel 50 times faster than before.
The study was conducted by Hiroaki Wake, Philip R. Lee, and R. Douglas Fields of the Nervous System Development and Plasticity Section of the NIHs Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD). Their findings appear online in Science Express.
Insulation begins to form on axons in the late stages of fetal development, but the process continues through childhood, adolescence, and into early adulthood, said Dr. Fields, the studys senior author. For example, infants cannot hold up their heads or walk until the appropriate motor axons become myelinated, and the frontal lobes of the brain, responsible for judgment and higher-level complex reasoning, are not fully myelinated until the early twenties.
Understanding how oligodendrocytes generate and help repair myelin could provide insight into how only the appropriate axons in the brain become insulated during development as people acquire skills, with the eventual goal of helping them do so more efficiently, Dr. Fields explained. Similarly, understanding the myelination process could lead to insights into disorders like multiple sclerosis, in which myelin is either damaged or destroyed. Moreover, understanding myelination may allow researchers to speed myelination and repair of axons recovering from injury.
Throughout the brain, oligodendrocytes and neurons exist side by side. The researchers placed mouse nerve cells and myelin-making oligodendrocytes together in a dish and stimulated the nerve cells with electrical pulses. After three weeks, they found that the nerve cells were wrapped in a myelin covering.
In a separate culture of neurons and oligodendrocytes, the researchers blocked the release of the molecule glutamate, a neurotransmitter. Neurotransmitters make it possible for signals to pass between cells. When glutamate release was blocked, very little myelin coating formed. Further experiments showed that after the electrical pulses and the release of glutamate, nerve cells and the neighboring oligodendrocytes began sending chemical signals back and forth. Then the oligodendrocytes started to make the protein used to form the myelin sheath. Specifically, receptors on the cell membrane of oligodendrocytes detect glutamate released by the axon, and this triggers the formation of what the researchers termed specialized adhesive signaling junctionspoints of contact between oligodendrocytes and axons that enable signals to be passed between the cells. Then the oligodentrocytes began depositing myelin on electrically active axons, but not on axons that were not electrically active.
In a previous study, Dr. Fields and his coauthors found that electrical activity in neurons stimulates other cells, called astrocytes, that also are involved in the myelination process.