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Revolutionizing Nerve Repair: Scientists Discover Key Protein in Mice

Salk Institute researchers have identified that the protein Mitf plays a crucial role in repairing nerve damage in peripheral neuropathy. This breakthrough paves the way for novel therapies that enhance nerve repair functions, potentially benefiting millions suffering from this condition.

Researchers at the Salk Institute have identified the protein Mitf as a key mediator in the repair processes of the peripheral nervous system in mice, suggesting a promising new therapeutic target.

Peripheral neuropathy affects over 3 million people annually in the United States, causing pain and loss of sensation due to nerve damage outside the brain and spinal cord. This condition can result from various causes including diabetes, injury, genetic disorders, and infections. Salk Institute scientists have made a significant discovery in mice regarding the repair of damaged nerves in peripheral neuropathy. They found that the protein Mitf activates the repair function in specialized Schwann cells of the nervous system.

Recently published in the journal Cell Reports<em>Cell Reports</em> is a peer-reviewed scientific journal that published research papers that report new biological insight across a broad range of disciplines within the life sciences. Established in 2012, it is the first open access journal published by Cell Press, an imprint of Elsevier.” data-gt-translate-attributes=”[{“attribute”:”data-cmtooltip”, “format”:”html”}]”>Cell Reports, this discovery could pave the way for innovative treatments aimed at enhancing the repair process and effectively treating peripheral neuropathy.

“We wanted to know what mechanisms control damage response in peripheral nerves under varying conditions—like acute trauma, genetic disorders, or degenerative diseases,” says senior author Professor Samuel Pfaff. “We found that Schwann cells, which are special cells in nerves that protect and support neurons’ axons, enter their repair state because of a pathway mediated by the protein Mitf.”

Samuel Pfaff and Lydia Daboussi

From left: Samuel Pfaff and Lydia Daboussi. Credit: Salk Institute

Understanding the Peripheral Nervous System

The peripheral nervous system is made up of all the nerves that branch out from the brain and spinal cord to give us sensation throughout our bodies. There are many cell types in peripheral nerves, but Pfaff and his team focus on understanding neurons, which transmit information throughout the nervous system, and Schwann cells, which protect healthy neurons and repair damaged ones.

The peripheral nervous system’s ability to repair damage is remarkable considering that the central nervous system—made up of the brain and spinal cord—is not able to repair damage. Yet, the mechanisms that orchestrate this feat have remained poorly understood.

Cross Section of Mouse Sciatic Nerves

Cross-section of mouse sciatic nerves. Credit: Salk Institute

To unravel how Schwann cells differentiate to begin repairing peripheral nerve damage, the researchers looked at mouse models of Charcot Marie Tooth disease (CMT), a type of hereditary neuropathy.

“Going into this project, I thought that when you have a genetic nerve degeneration disorder, cells are dying and recovery isn’t possible,” says first author Lydia Daboussi, a former postdoctoral researcher in Pfaff’s lab and current assistant professor at UC Los Angeles. “But our findings show that there are gene programs turned on by Mitf that repair some of the damage done in those chronic disease scenarios, and when you turn those programs off, disease symptoms get worse.”

The Potential of Schwann Cell Repair Programs

In mice with CMT, the researchers noticed that the Schwann cells completing the repairs had high levels of Mitf in their nuclei—where the genetic instructions for how to be a Schwann cell and how to conduct repairs are stored.

Upon investigation of this relationship between Mitf and Schwann cells, they found that Mitf was in the cytoplasm of Schwann cells until sensing neuronal damage. Damage then prompted Mitf to relocate from the cytoplasm of the cell to the nucleus, where it would direct the Schwann cell to make repairs.

To validate the importance of Mitf in creating repair Schwann cells, the researchers removed Mitf altogether. In cases of both trauma and CMT, nerve repair was arrested in the absence of Mitf—demonstrating that Mitf is required for peripheral nerve repair and regeneration.

According to Daboussi, Mitf acts like a fire extinguisher. Always there, sitting in the Schwann cell, unnoticed until damage occurs. And when that damage occurs, Mitf is ready to go and immediately turns on the cell’s repair functions.

Most surprising, noted Pfaff, was that Mitf was orchestrating these repairs during a chronic disease like CMT.

“Harnessing Schwann cell repair programs has great potential in treating chronic diseases,” says Pfaff, also the Benjamin H. Lewis Chair at Salk. “It’s possible that with targeted therapeutics, we can prompt more Schwann cells to repair peripheral nerve damage and push those repairs to completion in chronic cases. Furthermore, now that we have a better grasp on the repair mechanisms, we can see if it’s possible to initiate repairs in the brain stem and spinal cord, too.”

In the future, the researchers want to look more specifically at diabetes neuropathy—the most common peripheral neuropathy condition. They also hope to explore therapeutics that bolster this repair pathway to create more Schwann cells programmed to repair damage, regardless of if the source is trauma, genetics, or development over time.

Reference: “Mitf is a Schwann cell sensor of axonal integrity that drives nerve repair” by Lydia Daboussi, Giancarlo Costaguta, Miriam Gullo, Nicole Jasinski, Veronica Pessino, Brendan O’Leary, Karen Lettieri, Shawn Driscoll and Samuel L. Pfaff, 28 October 2023, Cell Reports.
DOI: 10.1016/j.celrep.2023.113282

Other authors include Giancarlo Costaguta, Miriam Gullo, Nicole Jasinski, Veronica Pessino, Brendan O’Leary, Karen Lettieri, and Shawn Driscoll of Salk.

The work was supported by the Sol Goldman Charitable Trust, Howard Hughes Medical Institute, National Institutes of HealthThe National Institutes of Health (NIH) is the primary agency of the United States government responsible for biomedical and public health research. Founded in 1887, it is a part of the U.S. Department of Health and Human Services. The NIH conducts its own scientific research through its Intramural Research Program (IRP) and provides major biomedical research funding to non-NIH research facilities through its Extramural Research Program. With 27 different institutes and centers under its umbrella, the NIH covers a broad spectrum of health-related research, including specific diseases, population health, clinical research, and fundamental biological processes. Its mission is to seek fundamental knowledge about the nature and behavior of living systems and the application of that knowledge to enhance health, lengthen life, and reduce illness and disability.” data-gt-translate-attributes=”[{“attribute”:”data-cmtooltip”, “format”:”html”}]”>National Institutes of Health (grants NCI CCSG: P30 014195, NCI CCSG: P30 014195, S10 OD023427, S10 OD026929, 1 RO1 NS123160-01), a George E. Hewitt Fellowship, a Salk Women & Science Fellowship, and a Jonas Salk Fellowship.

Source: SciTechDaily