Scientists uncover the role of a protein in production and survival of myelin-forming cells
The nervous system is a complex organ that relies on a variety of biological players to ensure daily function of the human body. Myelin—a membrane produced by specialized glial cells—plays a critical role in protecting the fibers that help carry messages throughout the body. In the central nervous system (CNS), glial cells known as oligodendrocytes are responsible for producing myelin. Now, a paper published today in Nature Communications explains how researchers at the Advanced Science Research Center (ASRC) at The Graduate Center of The City University of New York have uncovered the role of a protein known as “PRMT5” in the production of myelin and, ultimately, proper development and function of the CNS.
From infancy through adolescence, myelinating oligodendrocytes are generated in abundance in the human brain by progenitor cells in a process that is highly sensitive to hormones, nutrients and environmental conditions. In the adult brain, these progenitors cells—which similar to stem cells have the ability to differentiate into adult cells that perform specific tasks—serve as a reservoir for the generation of new myelin in response to learning and social experiences or to repair myelin loss after injury (e.g. after stroke or immune attack to myelin, as in Multiple Sclerosis).
The molecular mechanisms that generate myelin-forming oligodendrocytes are only partially understood, but through their research, ASRC scientists are one step closer to identifying them. Their work has pinpointed PRMT5 as a protein that regulates the molecules responsible for stopping or promoting the expression of certain genes that are needed for survival of oligodendrocytes and production of myelin. In other words, PRMT5 essentially acts as a traffic cop, allowing progenitor cells to become oligodendrocytes and stopping the biological signals that would interfere with myelin production.
“We were able to show that when PRMT5 is present, the progenitor cells are able to differentiate and become myelin-producing cells,” said Patrizia Casaccia, director of the ASRC’s Neuroscience Initiative and the Einstein Professor of Biology at Hunter College and at The Graduate Center, CUNY. “We discovered that progenitor cells lacking PRMT5 function essentially commit suicide while they are in the process of transitioning into myelin-forming cells. This discovery is important from a developmental and a translational standpoint. On one end, our findings allow a better understanding of how myelin is formed and possibly repaired when damaged. On the other end, they warn about potentially the possibility that pharmacological inhibitors of PRMT5, currently evaluated for their toxic function on glial tumor cells, might also kill healthy cells and prevent new myelin formation.
The study by Scaglione et al, identifies PRMT5 as a molecule that promotes new myelin formation , by acting on histones (proteins bound to DNA) and placing marks (CH3), which preclude the formation of obstacles to the differentiation of progenitor cells (by preventing KATs from depositing Ac marks)
ASRC researchers used three methods to eliminate PRMT5 and determine its role in myelin production in laboratory mice. First, they used CRISPR genetic ablation to target and eliminate the gene that produces PRMT5. In the second cohort, they used a pharmacological inhibitor to block activity of the protein. In the final cohort, they studied a group of knock-out mice who were born without the PRMT5-producing gene.
In each case, removing or blocking PRMT5 resulted in reduced progenitor cell differentiation and death of the cells that were attempting to become myelin producers.
“A logical next step was to try and determine how, in the absence or malfunction of PRMT5, we could help the progenitor cells differentiate and create myelin,” said Antonella Scaglione, lead author of the paper and a postdoctoral research associate with the ASRC. “We were able to identify ways to rescue the differentiation process of oligodendrocyte progenitors lacking PRMT5.”
The discovery of this correction was based on previous findings from the Casaccia’s laboratory about signals that interfere with myelin generation. These signals are carried out by enzymes called KATs (lysine acetyltransferases). The lab had previously shown that when KATs attach to nuclear proteins called histone, myelin formation is blocked. The researchers’ new work shows that blocking KATs can favor myelin formation and also overcome the effect of PRMT5 inhibitors. These findings could be critical to improving the survival of patients with malignancies that need to be treated with PRMT5 inhibitors.
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