Summary: Researchers shed light on the largely unstudied process of synaptic pruning in brain development, using mouse mitral cells, a neuron type in the olfactory system. The research reveals that neurons receiving a neurotransmitter signal are protected via specific chemical pathways while other dendrites in the same cell are triggered to undergo pruning.
The study uncovers a nuanced ‘protection/punishment’ system governing synaptic pruning. Understanding this process could help in comprehending neurophysiological disorders like schizophrenia and autism.
- The neurotransmitter glutamate is crucial in synaptic pruning. When glutamate binds to its receptor NMDAR in a dendrite, it suppresses a molecule called RhoA, which is part of the pruning machinery, thereby protecting that dendrite from being pruned.
- Dendrites not receiving the direct glutamate signal undergo a depolarization process that triggers the activation of RhoA, thereby promoting their pruning. This discovery provides valuable insight into how certain neuronal connections are preserved while others are eliminated during development.
- The researchers used mouse mitral cells for their study because they transition from having multiple connections to a single strong one during development, mirroring the pruning process seen in the broader brain development context.
Source: Kyushu University
Researchers at Kyushu University have uncovered the mechanisms of a fundamental yet critically under-looked phase in brain development: synaptic pruning.
Using mouse mitral cells—a type of neuron in the olfactory system—the team found that when neurons receive a neurotransmitter signal, the receiving dendrite is protected through a series of chemical pathways. At the same time, the depolarization triggers other dendrites of the same cell to go through a different pathway that promotes pruning.
Their study was published in the journal Developmental Cell.
How neurons connect and remodel themselves is a fundamental question in neurobiology. The key concept behind proper networking is in neurons forming and strengthening connection with other neurons while pruning excessive and incorrect ones.
“A common phrase in neural circuit remodeling is ‘fire together wire together’ and ‘out of sync, lose your link.’ The former describing how neurons that pass signals between each other tend to strengthen connections, whereas the latter explains that without said signaling that connection diminishes,” explains Professor Takeshi Imai from Kyushu University’s Faculty of Medical Sciences, who led the study.
“It’s a refining process that is fundamental for proper brain maturation.”
Over the decades, researchers—including Prof Imai—have explored the fundamental process of how neurons form and strengthen their connections. However, there had been one major gap in the process that few people were examining: how the connections are eliminated.
“The elimination of neuronal connections, what we call pruning, was something everybody in the field knew about and observed. But if you look at the literature, there was a lack of study on the exact mechanism that drove the process,” explains first author Satoshi Fujimoto.
Elimination of connections happen everywhere in the nervous system, for example in neuromuscular junctions, the neurons that send signals to your muscles to move. At first, the muscle fibers receive inputs from many motor neurons.
As you grow, these connections are finetuned, where some are strengthened, and others are eliminated, until just one neuron connects to one muscle fiber. It is why you have awkward motor control and coordination at an early age.
“We decided to investigate what exactly happens in neurons during remodeling, so, we looked into using mouse mitral cells, a type of cell housed in the olfactory bulb, the brain center involved in our sense of smell. In adults, mitral cells have a single connection to a signaling waystation called the glomerulus. But in early development mitral cells send branches into many glomeruli,” states Fujimoto.
“As time progresses, these branches get pruned to leave a single strong connection. In the end, the mitral cells can sniff out only a specific type of smell.”
First, the team found that spontaneous waves of the neurotransmitter glutamate in the olfactory bulb facilitate dendrite pruning. The team then focused on the mitral cell’s inner signaling pathways. What they found was a unique protection/punishment machinery that would strengthen certain connections and kickoff the pruning of others.
“We found that in the mitral cells it was the signaling from glutamate that was essential for pruning. When glutamate binds to its receptor NMDAR in a dendrite, it suppresses the pruning machinery molecule called RhoA,” continues Fujimoto. “This ‘save-me’ signal is important to protect it from pruning.”
Upon the glutamate input, the mitral cell also depolarizes and fire a signal. The team also found that depolarization triggers the activation of RhoA in other dendrites of the same cell, and kicking off the pruning process. Simply put, the dendrite that receives the direct glutamate signal is protected, while the other dendrites get pruned.
“This ‘punishment’ signal for synapse elimination only acts on non-protected synapses, and it explains how only a strong connection becomes the winner and all the others mediating weak and noisy inputs become the losers,” Imai explains.
The team’s findings reveal new information of an over-looked but critical phase in neural development.
“Proper pruning of neuronal connections is just as important as the strengthening of the network. If it goes awry in either direction it can lead to different kinds of neurophysiological disorders. Too few connections have been linked to schizophrenia, whereas too many connections have been found in people with autism spectrum disorder, for example.” says Imai.
“To understand these sorts of pathologies we need to look carefully at every step of development.”
About this neuroscience research news
Original Research: Open access.
“Activity-dependent local protection and lateral inhibition control synaptic competition in developing mitral cells in mice” by Takeshi Imai et al. Developmental Cell
Activity-dependent local protection and lateral inhibition control synaptic competition in developing mitral cells in mice
In developing brains, activity-dependent remodeling facilitates the formation of precise neuronal connectivity. Synaptic competition is known to facilitate synapse elimination; however, it has remained unknown how different synapses compete with one another within a post-synaptic cell.
Here, we investigate how a mitral cell in the mouse olfactory bulb prunes all but one primary dendrite during the developmental remodeling process. We find that spontaneous activity generated within the olfactory bulb is essential.
We show that strong glutamatergic inputs to one dendrite trigger branch-specific changes in RhoA activity to facilitate the pruning of the remaining dendrites: NMDAR-dependent local signals suppress RhoA to protect it from pruning; however, the subsequent neuronal depolarization induces neuron-wide activation of RhoA to prune non-protected dendrites. NMDAR-RhoA signals are also essential for the synaptic competition in the mouse barrel cortex.
Our results demonstrate a general principle whereby activity-dependent lateral inhibition across synapses establishes a discrete receptive field of a neuron.