A "fountain of youth" that sustains the production of new neurons in the brains of rodents is also believed to be present in the human brain. The existence of a vital support system of cells around stem cells in the brain explains why stem cells by themselves can't generate neurons in a lab dish, a major roadblock in using these stem cells for therapy.
New research has found that neighboring "epithelial-like" ependymal cells – not stem cells themselves – maintain a special structure that keeps neural stem cells, "neurogenic," able to make new neurons.
When neural stem cells are harvested for growth in culture, however, these ependymal cells are not removed along with them.
In a series of experiments, the researchers found that the generation of new neurons depended on what Kuo calls the "ugly sibling" of the stem cells, the ependymal cell that has long, moving, hair-like cilia that cover its surface. Kuo decided to study these cells because the lateral ventricles in the brain, where adult neural stem cells reside, are also the last area of a developing brain that grows ependymal cells.
"The common radial glial progenitors in the developing nervous system prior to birth give rise to both the ependymal cells and the adult stem cells," Kuo said. "So it made sense to study these niche cells as well as the stem cells."
"There is this fountain of youth inside the adult brain that actively makes new neurons," Kuo said. "Yet we don't know how this fountain is constructed or maintained."
Kuo and his colleagues found that the Foxj1 transcription factor, a class of master proteins that turn other genes on and/or off, is critical to instruct ependymal cells to change shape and assemble into pinwheel-like architecture surrounding stem cells. He said the lateral membranes of mature ependymal cells are shaped like machine cogs or fingers that lace together.
The researchers determined that the structural protein Ankyrin 3 was turned on by Foxj1 in these ependymal cells to provide structural support for the delicate neural stem cells. Signals generated by this structural support will probably be important for instructing introduced neural stem cells to make neurons in therapeutic settings, he said.
Kuo said he would not have examined the role of ependymal cell Foxj1 in relation to neural stem cells if not for his Cell Biology Chair, Brigid Hogan, Ph.D., whose lab next door is a world leader in understanding adult lung and airway stem cell function. Likewise, Kuo said pioneering work on ankyrins by Duke Cell Biology and Howard Hughes Medical Institute Investigator Vann Bennett, M.D., Ph.D., paved the way for study of these proteins in the neural stem cell environment.
"Understanding the environmental control of neuron production in the adult brain will be crucial for future therapeutic strategies using human stem cells to replace neurons," Kuo added.
Adapted from the Duke University Medical Center announcement.