Ultrahigh resolution, high-speed imaging of fruit fly brains has allowed University of Oregon scientists to capture mechanical motions that stem cells use to make neurons, the cells that make up the brain.
The motions coordinate cell division during differentiation, when some newly born cells become neurons. Differentiation is essential for building the circuitry that underlies human cognition and emotions, said Ken Prehoda, a professor in the UO’s Department of Chemistry and Biochemistry.
Drosophila fly brains have some 100,000 neurons, while human brains have more than 50 billion. Developmental research in Drosophila often leads to advances in human medicine.
The discovery, Prehoda said, suggests that the mechanical process is vital to understanding brain development and, potentially, for regenerating neurons and their connections following injuries.
“To make so many neurons, the developing brain acts like a factory with individual stem cell ‘machines’ continually producing neurons,” Prehoda said. “We discovered that stem cells have more in common with real machines on a factory floor than previously appreciated, in that they undergo a mechanical cycle when producing each neuron.”
In the project, LaFoya used spinning-disk confocal microscopy to examine fruit fly brains with their stem cell membranes embedded with fluorescent markers. That unveiled the membrane dynamics of neural stem cells and their progeny at high resolution, revealing the mechanical cycle as each neuron was produced.
To make neurons, Prehoda said, neural stem cells must place special molecules, proteins called fate determinants, into one of two daughter cells that result from division. How that was done had been unclear despite many previous studies of physical interactions in which fate determinants are involved.
In a 2019 study in the journal eLife, Prehoda and Krystal Oon, a graduate student in the Institute of Molecular Biology, reported that proteins undergo movements along the membrane, but what drove the movement was unknown.
“Mechanical forces within the cell segregate components that are responsible for cellular identity after division,” LaFoya said. “After the cell divides in two, because of these forces, one cell will remain a stem cell while the other will go on to become a neuron.”
The cellular-scale mechanical forces revealed in the imagery were so strong that surrounding cell membranes became highly distorted before returning to normal, Prehoda added. Understanding the process from beginning to end, he said, could have implications for regenerative therapies.
The project was funded by the National Institutes of Health. Imaging was done in the UO’s Genomics & Cell Characterization Core Facility with a spinning-disk confocal microscope purchased with a grant from the M.J. Murdock Charitable Trust through the UO Foundation.
This story was originally published by the University of Oregon