New study finds external stimulation impacts white matter development in the postnatal brain

NG2 cells can develop into oligodendrocytes progenitor cells that generate myelin, the protective material around the axons of neurons, but this is based on functional and developmental interactions with outside stimuli. With this kind of plasticity, or ability to change and mold a cell in different ways, the researchers were able to determine that sensory stimuli can control the number and positioning of developing NG2 cells.

"Understanding how external stimulation and experience impact the development of NG2 cells means that we can try to modulate these factors to help regulate and promote the expansion of these cells. This could ultimately have an impact on white matter diseases," stated Vittorio Gallo, PhD, study coordinator and Director of the Center for Neuroscience Research at the Children's Research Institute. "We will now investigate in more detail how sensory experience can regulate NG2 cell development, particularly how experience activates specific genes and molecular pathways in these cells."

Collectively called NG2 progenitors, these cells also serve as the primary source of cells to regenerate oligodendrocytes and myelin in the postnatal brain. Without myelin, the brain does not function properly. Myelination can be impaired for a number of reasons, resulting in mental retardation and developmental disabilities. Myelination, white matter growth and repair, and the study of complex mechanisms of pre- and postnatal brain development are a key focus of the Center for Neuroscience Research at Children's National, which also houses the White Matter Diseases Program, one of the largest clinical programs in the country for treating children with disorders that cause the brain's white matter to degenerate.

Provided by Children's National Medical Center