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Williams Syndrome Model Gets Insight into Human Social Brain

August 10, 2016 By University of California - San Diego

In a study spanning molecular genetics, stem cells and the sciences of both brain and behavior, researchers at University of California San Diego, with colleagues at the Salk Institute for Biological Studies and elsewhere, have created a neurodevelopmental model of a rare genetic disorder that may provide new insights into the underlying neurobiology of the human social brain.

The findings are published in the August 10 online edition of Nature.

Scientists investigated Williams syndrome or WS, a rare genetic condition caused by deletion of one copy of 25 contiguous genes on chromosome 7, out of an estimated 30,000 genes in the brain. WS affects one in 10,000 people worldwide, and an estimated 20,000 Americans. The condition occurs equally in both genders and across cultures.

WS results in a host of medical problems as well as a specific heart defect. Persons with the deletion typically display a distinctive face with a small, upturned nose, wide mouth, full lips and small chin and may also have dental and orthopedic problems. Neurologically, they have developmental delays, with severe spatial deficits, yet relative strengths in language use and face processing.

“An interesting aspect is the typical hyper-social predisposition,” said study co-author Ursula Bellugi, Ed.D., director of the cognitive neuroscience lab at Salk and an adjunct professor at UC San Diego who has studied WS for years. “Persons with the WS deletion tend to be overly friendly, overly trusting, drawn to strangers, yet anxious.”

But Bellugi said it has not been clear how genetics links to the behavioral aspects of WS. “A human model for the disease could fill in the scientific gaps and would help to understand the mechanisms behind the disorder. WS is an elegant model for being able to go across levels,” she said.

Co-senior study author Alysson Muotri, Ph.D., associate professor of pediatrics and cellular and molecular medicine at UC San Diego School of Medicine, became intrigued by WS because the condition is so different from his usual research focus on autism, which is characterized by lower sociability and language skills.

“I was fascinated on how a genetic defect, a tiny deletion in one of our chromosomes, could make us friendlier, more empathetic and more able to embrace our differences,” Muotri said.

In recent years, Muotri and colleagues have created in vitrocellular models of autism using reprogrammed induced pluripotent stem cells (iPSC) derived from discarded baby teeth of children with autism, work dubbed the “tooth fairy project.” They did so again here.

The team began with dental pulp cells extracted from teeth donated by young children with WS. The cells were reprogrammed to become neural progenitor cells able to form functional neuronal networks resembling the developing cortex of the human brain in a dish.

“We discovered that WS neural progenitor cells failed to proliferate due to high levels of cell death,” Muotri said. “And as a consequence of the lower replication of progenitor cells, WS brains have reduced cortex surface area.” The observation was validated using magnetic resonance imaging of live study participants by Eric Halgren, PhD, professor in the Department of Neurosciences at UC San Diego School of Medicine, and colleagues.

Cultured WS neurons have a distinct morphology. They are more arborized (treelike, with many dendritic branches) than neurons derived from typically developing individuals. “At the functional level, they make more synapses or connections to other neurons than what you would expect,”  Muotri said. “That might underlie the WS super-social aspect and their gregarious human brain, giving insights into autism and other disorders that affect the social brain.”

The neuronal morphology was confirmed using a rare collection of WS postmortem brain tissue by Katerina Semendeferi, Ph.D., co-senior author and professor at UC San Diego Department of Anthropology. “One striking observation was that these cortical neurons in WS individuals are more complex than controls (typically developing children of same age). The morphological alterations that presumably appeared during WS gestation are kept postnatally.”

Muotri noted that the research represents one of the first efforts to use iPSCs and brain in-a-dish technology to generate novel insights about a disease process and not simply replicate data from other models.

But beyond that, he believes studying WS may help explain what makes humans social beings – a key development in the evolution of humanity. “It was our social power that made us a collaborative species,” Muotri said, “capable of dramatic transformation of our environment by creating poetry, music and technology.”

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