During embryonic development, the entire nervous system, the skin and the sensory organs emerge from a single sheet of cells known as the ectoderm. While there have been extensive studies of how this sheet forms all these derivatives, it hasn't been possible to study the process in humans -- until now.
Rice bioscientist Aryeh Warmflash, graduate student George Britton and their colleagues have created a system in which all of the major cell types of ectoderm are formed in a culture dish in a pattern similar to that seen in embryos.
This technique, based on controlling the geometry of stem cell colonies with microscale patterns, has helped them make the most comprehensive analysis yet of signaling pathways that drive patterning of human ectoderm.
"There are very few possible signals the embryo uses to generate the wide variety of cell types that arise," Britton said. "We want to understand the timing of these signals and how the cells interpret them in time to generate this variety."
Their study was published as a highlighted article in Development, which also published a lengthy interview with the researchers.
It revealed that the balance between two signaling pathways, BMP and Wnt, are both critical, and even a bit adaptable as they orchestrate patterning in the ectoderm. The logic they employ ultimately drives ectodermal cells to their fates, but the research showed they can take more than one road to get there.
Britton said the micropatterned plates and a better understanding of how the signaling pathways work let them manipulate stem cell colonies to form unusual patterns at the start, but ultimately they always seemed to converge at the same place. "We found different trajectories of the signals that arrived at the same pattern," he said.
That suggested the system by which stem cells become neurons, neural crest cells, neurogenic placodes and epidermis cells is pretty robust.
"A lot of people are interested in the transcription factor network that directs neural crest emergence, so this is a powerful system to dissect the signals that contribute to that logic," Britton said. "That was one thing we feel we contributed to the field.
"There's also the idea that cells that have the ability to interpret relative levels of BMP and Wnt to incorporate the appropriate fate decision," he said. "In the embryo, cells are moving around quite a bit in a space where signals and the ligands they're exposed to are also moving around. It might be that cells are reading the relative levels to determine a certain fate."
The researchers observed that the relative activity of BMP and Wnt signaling determines cells' decisions to become either neural crest or placodal cells, while BMP alone initiates and controls the size of the surface ectoderm, all within about the first four days.
"Four days is about right in the sense that cells are starting to make decisions: 'I'm going to be a placodal cell, I'm going to be a neural crest cell, I'm going to be neural fate and I'm going to an epidermal fate," Britton said.
"We see that approximately a day or two after BMP treatment. But it's hard to put a finger on whether these are the final patterns," he said. "We'd have to do a more careful observation to make sure those placodal cells don't change to neural crest cells, or vice versa. That will give us information on how these lineages and fates settle into a final pattern, maybe by day 6 or 7."
He said future studies will further refine their understanding of how signaling patterns work, as well as how the development of all the germ layers collaborate.
"Until now, studies of human stem cells differentiating to ectodermal fates were mostly about how to get all the cells in your culture dish to become a particular cell type; for example, how to make a dish full of neurons," Warmflash said. "We are interested in a different question: How do cells interact with each other to make patterns of different cell fates? The system we developed does this outside the embryo and is allowing us to begin to tackle this question."
Co-authors of the paper are Rice alumni Idse Heemskerk, now at the University of Michigan Medical School, and Rachel Hodge, now at UCLA; and Amina Qutub, an associate professor of biomedical engineering at the University of Texas at San Antonio. Warmflash is an assistant professor of biosciences and bioengineering.
The National Institutes of Health, through the National Institute of General Medical Sciences; the National Science Foundation, the Cancer Prevention and Research Institute of Texas, the University of Texas STARS program and the Simons Foundation supported the research.
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