Many living creatures possess exceptional abilities that set them apart from other species. Cheetahs can run up to 60 miles per hour; ants can lift 100 times their body weight; flatworms can regrow amputated body parts. Scientists have spent decades studying the mechanisms that drive such remarkable feats, with the hopes that any secrets they uncover might lead to new perspectives in human biology and new ways to enhance health and ameliorate disease.
Now, researchers at the Stowers Institute have identified a key molecule that directs stem cells in the planarian flatworm to make copies of themselves. The molecule, called EGFR-3, is part of a cascade of signals that seem to control the way these cells divide and differentiate in response to near-lethal levels of radiation.
The finding, which appears online August 11, 2016, in the journal Developmental Cell, has important implications for advancing regenerative medicine and for developing more effective cancer therapies.
"All the genes in this signaling cascade are conserved, from planaria on up to humans. A similar process could also be taking place within our very own cells, we just don't know it," says Alejandro Sánchez Alvarado, Ph.D., an investigator at the Stowers Institute and Howard Hughes Medical Institute, who is the senior author of the study. "In fact, anything that perturbs our body - aging, injury, even a spicy meal - can affect our stem cell functions. If we understand better how planarians regulate the population dynamics of their stem cells, it may provide a clue for addressing our own pathologies."
Planarians are world-renowned for their regenerative properties. Split one down the middle, and two identical organisms will appear in its place. Cut a fragment 1/279th the size of the original animal and it will regenerate a complete animal. This ability originates in a special group of adult stem cells called neoblasts that are spread throughout the bodies of these freshwater worms. Several years ago, researchers tested the limits of these resilient creatures by subjecting them to near-lethal doses of radiation. They found that even if just a single neoblast remained, it was enough to replenish the entire population of planarian stem cells.
In this study, Sánchez Alvarado wanted to pinpoint the exact signals that shaped these dramatic population dynamics. Kai Lei, Ph.D., a postdoctoral scientist in his lab, decided to go after the usual suspects - namely, the EGF, FGF, Insulin, VEGF, TGF-beta, Wnt/beta-catenin, Hedgehog, and Notch signaling pathways - that have been associated with stem cells and thus might play a role in this process. First, Lei and colleagues used an advanced molecular technique called RNA interference to silence different genes in the suspected signaling pathways. Next, he subjected planaria to a dose of radiation that would kill most, but not all, of their resident neoblasts. Then, he waited to see how each silenced gene affected the ability of the neoblasts to recover, repopulate, and restore the survival of the irradiated animals.
The researchers discovered that the egfr-3 gene was required for neoblast repopulation. This gene codes for a protein that sits on the surface of cells and binds another protein - called epidermal growth factor - known to stimulate growth, proliferation, and differentiation in other cell types. When they confirmed their findings by using a fluorescent staining to illuminate the EGFR-3 protein on the neoblasts, they stumbled upon something curious. The proteins sat on the top of the cell, like the researchers had expected, but rather than being randomly distributed across the entire surface, they were clumped together on one side, like an unruly head of hair.
The uneven distribution of EGFR-3 suggested that the protein might be involved in a phenomenon known as asymmetric cell division, which along with symmetric cell division constitute the two ways that cells make copies of themselves. In asymmetric cell division, the mother cell divides into two daughter cells that have different fates - one might be a neoblast, another a muscle cell or photoreceptor cell. In symmetric cell division, the mother cell divides into two daughter cells that share all the same attributes.
"Even though asymmetric cell division has long been proposed to exist in planarians, our study provides the first direct molecular evidence of its existence," says Lei. He showed that when EGFR-3 was functioning normally, irradiated neoblasts divided by asymmetric cell division half of the time and by symmetric cell division the other half of the time. But when he silenced EGFR-3, asymmetric cell division was impaired.
The researchers believe that this particular pathway might be providing a type of quality control to ensure that mistakes made to the genome either through irradiation or other forms of damage are not propagated. In fact, when they looked further down the pathway, Sánchez Alvarado and his team found several genes involved in DNA repair.
"Asymmetric cell division may be a way of getting rid of the bad apples. We don't have proof yet, but we think that this signaling pathway helps to shuffle along the cells that carry defects, giving them different fates so they no longer make more stem cells (neoblasts). The prediction would be that only the cells with the best DNA get to stick around and serve as the template for future generations -- something we need to test next," said Sánchez Alvarado.
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