Glial Cells Eating of Synapses May Enhance Learning and Memory

Summary: Bergmann glial cell synaptic engulfing in the cerebellum was enhanced during motor learning in mice.

Source: Tohoku University

Tohoku University researchers have shown that Bergmann glial cells, astrocyte-like cells in the cerebellum, ‘eat’ their neighboring neuronal elements within healthy living brain tissue.

Synapses – structures that allow neurons to pass signals to one another – are regularly pruned throughout a brain’s development to improve its efficiency. Disruption of this is thought to lead to various brain disorders.

The researchers’ findings, which were detailed in the journal Nature Neuroscience, discovered that Bergmann glial engulfing of synapses was enhanced during motor learning in mice’s cerebellum, an important brain region for learning.

Moreover, pharmacological blocking this engulfment inhibited synaptic structural changes, resulting in part of the learning and memory process being lost.

Glial cells, non-neuronal cells occupying about half of the brain, were previously believed to be like glue – merely filling the gap between neurons. However, recent findings show that glia encode information in their own unique way.

“Glia are, of course, not another subcategory of neurons,” says Professor Ko Matsui of Tohoku University’s Super-network Brain Physiology lab, who led the research. “We have yet to uncover the glial impact on information processing.”

When cells engulf neighboring cells to flush out debris and pathogens, it is called phagocytosis. Phagocytosis by microglia, immune cells in the brain, in damaged and diseased brain tissue has long been recognized.

Recent reports have established that astrocytes and microglia phagocytose neuronal elements, including synapses during early brain development or when dramatic neuronal network remodeling occurs in the diseased brain.

Tracing engulfed materials is challenging in healthy brains, since the lysosomes in the glia quickly degenerate the proteins.

This shows glial cells
A 3D reconstructed synaptic structure capturing glial phagocytosis. A represents part of a 3D reconstructed Purkinje cell dendrite (yellow). Multiple spines are found at a high density along the dendrite. In many of the spines, aberrant protrusions were found (protrusions from the spine are colored in red). These protrusions were observed at a high frequency in tissue taken from the mouse cerebellum after motor learning. The protrusions were engulfed by Bergmann glia processes. Images were captured by focused ion beam scanning electron microscopy (FIB-SEM) and 3D reconstructed using computer software. B shows a close up of a presynaptic bouton (cyan) and a postsynaptic spine (yellow). Red represents the synaptic contact plane of the pre and postsynaptic specializations. Normal synaptic structures are shown in semi-transparent colors. The synaptic structures engulfed by Bergmann glia processes are shown in opaque colors. A portion of both pre and postsynaptic structures are undergoing phagocytosis by Bergmann glia, which results in volume reduction of the synaptic structure. Phagocytosis of the synaptic structure by glia was found more frequently in brain tissue taken after motor learning. Credit: Morizawa & Matsui

Matsui and his team turned to the degeneration-resistant fluorescent protein pHRed to alleviate this problem. Using high-resolution 3D electron microscopy, they captured the Bergmann glia nibbling on synapses parts and other neuronal parts in adult healthy mice brains.

Furthermore, glial phagocytosis was enhanced in brain tissues taken after cerebellar-dependent motor learning tasks. When phagocytosis was pharmacologically blocked, some of the learning was lost.

“Our finding provides a novel glial mechanism in synaptic plasticity linking learning and memory. It is possible that the phagocytic capacity of glia might be variable under the certain states of our mind and glia may play a pivotal role in meta-plasticity of memory formation,” said Matsui.

Lead study investigator Dr Yosuke Morizawa says that their discoveries could have possible implications for explaining why synaptic shrinkage and loss occur in depression, schizophrenia, and Alzheimer’s disease.

The team’s next step is to see if glial phagocytosis of synapses malfunctions in animal models of these diseases.

“A therapeutic strategy designed to target glial phagocytosis might enhance memory and treat certain brain disorders,” added Matsui.

About this memory and learning research news

Author: Press Office
Source: Tohoku University
Contact: Press Office – Tohoku University
Image: The image is credited to Morizawa & Matsui

Original Research: Closed access.
Synaptic pruning through glial synapse engulfment during motor learning” by Ko Matsui et al. Nature Neuroscience


Synaptic pruning through glial synapse engulfment during motor learning

Synaptic pruning is a fundamental process of neuronal circuit refinement in learning and memory. Accumulating evidence suggests that glia participates in sculpting the neuronal circuits through synapse engulfment.

However, whether glial involvement in synaptic pruning has a role in memory formation remains elusive.

Using newly developed phagocytosis reporter mice and three-dimensional ultrastructural characterization, we found that synaptic engulfment by cerebellar Bergmann glia (BG) frequently occurred upon cerebellum-dependent motor learning in mice.

We observed increases in pre- and postsynaptic nibbling by BG along with a reduction in spine volume after learning. Pharmacological blockade of engulfment with Annexin V inhibited both the spine volume reduction and overnight improvement of motor adaptation.

These results indicate that BG contribute to the refinement of the mature cerebellar cortical circuit through synaptic engulfment during motor learning.

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