Manipulating astrocytes affects long-term memory, researchers discover

Saying goodbye to traumatic memories: Astrocytic manipulation of the fate of memory
Selective suppression of long-term memory formation through ChR2 photoactivation of amygdala astrocytes. The experiments suggest the presence of parallel processes governing short-term and long-term memory formation, respectively. Credit: Hiroki Yamao, Ko Matsui

One of the most powerful assets of the brain is that it can store information as memories, allowing us to learn from our mistakes. However, some memories remain vivid while others become forgotten. Unlike computers, our brains appear to filter which memories are salient enough to store.

Researchers from Tohoku University have discovered that part of the memory selection process depends on the function of astrocytes, a special type of cell that surrounds neurons in the brain. They showed that artificially acidifying the astrocytes did not affect short-term memory but prevented memories from being remembered long-term.

The findings are published in the journal Glia.

The researchers implemented a technique called “optogenetics” to manipulate the astrocytes by shining light onto them through optical fibers inserted in the mice’s brains. This enabled the team to directly stimulate and either acidify or alkalinize the astrocytes in that area. They focused on the functions of astrocytes in the amygdala, a brain region known to be crucial for regulating emotion and fear.

Saying goodbye to traumatic memories: Astrocytic manipulation of the fate of memory
Mice inherently possess a selective filtering mechanism that enhances the memory of intense experiences; however, this filtering function was inhibited by ArchT photoactivation of astrocytes in the amygdala. Additionally, the natural forgetting process over three weeks was suppressed by the light stimulation of ArchT-expressing astrocytes. Credit: Hiroki Yamao, Ko Matsui

A mild electrical shock was delivered to mice in an experiment chamber. When placed back in the same chamber, the mice remembered the shock and froze as a natural response. In comparison, the mice who had their astrocytes acidified immediately after the mild shock were able to temporarily hold onto the fear memory, but they forgot it by the next day. This shows that acidifying the astrocytes did not affect short-term memory but prevented the memories from being remembered long-term.

A different effect was seen for mice who had their astrocytes alkalinized. When tested three weeks later, control mice typically showed signs of forgetting, demonstrated by a decrease in freezing responses. However, mice whose astrocytes were alkalinized immediately after a strong shock still displayed strong fear responses even after three weeks.

This suggests that astrocytes play a key role in determining whether memories are erased or preserved for a long time, immediately after a traumatic event.

Saying goodbye to traumatic memories: Astrocytic manipulation of the fate of memory
Astrocytes are capable of triggering fear. Astrocyte ChR2 photoactivation alone induced freezing responses akin to those observed after receiving an electric foot shock. In contrast, astrocyte ArchT photoactivation suppressed the freezing responses following a footshock. Credit: Hiroki Yamao, Ko Matsui

While it is generally believed that memories are formed in a continuous process whereby short-term memories gradually solidify and become long-term memories, this research suggests they may actually develop in parallel.

“We believe that this could change the way we understand memory formation,” says Professor Ko Matsui of the Super-network Brain Physiology lab at Tohoku University, who led the research. He added, “The effect of astrocytes on memory likely also depends on various contexts, including mental, social, or environmental factors.”

Lead investigator Hiroki Yamao believes astrocytes could hold the key to understanding emotional changes and memory formation. “This may be just a glimpse of how astrocytes affect emotional information processing,” Yamao explains.

“Our next goal is to uncover the mechanisms by which astrocytes regulate emotional memory. Understanding these processes could pave the way for therapies that prevent traumatic memories from forming, offering a valuable approach to treating disorders like post-traumatic stress disorder (PTSD) by intervening in memory formation,” says Yamao.

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