by Luis Sandoval, Cold Spring Harbor Laboratory
A cross-section of the somatosensory cortex in a young mouse brain. A key receptor protein named mGluR1 (green) is necessary to prime sensory circuits early in life, affecting how the mouse senses the world through touch. Credit: Pouchelon lab/Cold Spring Harbor Laboratory
Not everything in the brain is meant to last. As our brains assemble, trillions of neural connections have to be built or torn down at the right time and place. Otherwise, the seeds of disorders like autism can take root.
Cold Spring Harbor Laboratory Assistant Professor Gabrielle Pouchelon studies how the brain is wired early in life. In doing so, she hopes to find the origins of various brain dysfunctions and new ways to treat them.
In a new study published in the journal Nature Communications, Pouchelon and her team zero in on a process known as pruning. This is when the brain removes unnecessary connections between neurons. The pruning of long-lasting connections is relatively well-known. Pouchelon's team focuses on special early connections that get cut to make way for long-lasting circuits in the mature brain. Though temporary, these early connections may play a critical role in shaping developing brain circuits.
Pouchelon's lab has now discovered that a receptor protein named mGluR1 helps regulate the timing of these temporary connections in the mouse brain. Her team found that without mGluR1, neural connections stick around too long in the brain region that controls and processes touch via the whiskers. When the sensory circuit fails to mature properly, the mice demonstrate atypical behaviors. For example, they don't stand on their hind legs and sniff around the way other mice do.
Importantly, the team notes that this critical step in circuit development occurs during the first week after birth. "The way the receptor works seems to be different than what has been described in adulthood," Pouchelon says.
"In the context of neurodevelopmental disorders, that means when we try to target developmental defects, we could have a totally different therapeutic effect at different stages during development."
Pouchelon's team hopes their discovery may serve as a guide for designing future therapeutics to treat brain dysfunction early. "The brain is a wonderful machine whose job is to adapt," says Dimitri Dumontier, the postdoc in Pouchelon's lab who co-led this study.
"So, when you study neurodevelopmental disorders in adults or even teenagers, it is difficult to identify which mechanisms are causing the symptoms. That is why understanding early milestones of brain development is key."
The hope is that by figuring out exactly how the brain matures, scientists can rescue this process early. This could help prevent symptoms of neurological disorders like autism from showing up in the first place.
After all, the world is difficult enough to navigate as is. Pouchelon and Dumontier's work could someday help make life easier for countless young people.
More information: Deepanjali Dwivedi et al, Metabotropic signaling within somatostatin interneurons controls transient thalamocortical inputs during development, Nature Communications (2024). DOI: 10.1038/s41467-024-49732-w
Journal information: Nature Communications
Provided by Cold Spring Harbor Laboratory
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