This shows microglia.
The newly identified mechanisms could be important for maintaining behaviors within the healthy range under normal conditions. Credit: Neuroscience News

Microglia’s Role in Controlling Anxiety and OCD

Summary: A new study reveals how microglia can regulate anxiety and obsessive-compulsive spectrum disorder (OCSD) behaviors.

Traditionally overlooked in favor of neurons, specific microglia populations were found to both stimulate and suppress these behaviors, thus acting as both a “brake” and “accelerator”.

They achieved this by employing optogenetics to stimulate different microglia populations in the brain. These new findings open up promising avenues for targeted therapies.

Key Facts:

  1. Microglia, a minor cell type in the brain, play a significant role in regulating anxiety and OCSD behaviors.
  2. Different microglia populations can both stimulate and suppress these behaviors, akin to acting as a “brake” and “accelerator”.
  3. This groundbreaking research could lead to targeted therapeutic approaches for excessive anxiety and OCSD behaviors.

Source: University of Utah

The pandemic and its aftermath have raised anxiety to new levels. But the roots of anxiety-related conditions, including obsessive-compulsive spectrum disorder (OCSD), are still unclear.

In a new study, University of Utah Health scientists discovered insights into the importance of a minor cell type in the brain—microglia—in controlling anxiety-related behaviors in laboratory mice. Traditionally, neurons—the predominant brain cell type—are thought to control behavior.

The researchers showed that, like buttons on a game controller, specific microglia populations activate anxiety and OCSD behaviors while others dampen them. Further, microglia communicate with neurons to invoke the behaviors.

The findings, published in Molecular Psychiatry, could eventually lead to new approaches for targeted therapies.

“A small amount of anxiety is good,” says Nobel Laureate Mario Capecchi, Ph.D., a distinguished professor of human genetics at the Spencer Fox Eccles School of Medicine at University of Utah and senior author of the study.

“Anxiety motivates us, spurs us on, and gives us that extra bit of push that says, ‘I can.’ But a large dose of anxiety overwhelms us. We become mentally paralyzed, the heart beats faster, we sweat, and confusion settles in our minds.” 

The newly identified mechanisms could be important for maintaining behaviors within the healthy range under normal conditions. Under pathological conditions, the mechanisms could drive behaviors that become debilitating, Capecchi says.

“This work is unique and has challenged the current dogma about the role of microglia function in the brain,” says Naveen Nagajaran, Ph.D, a geneticist and neuroscientist at U of U Health and the study’s lead author.

Manipulating microglia

Mice with OCSD-like behaviors can’t resist grooming themselves. They lick their bodies so much that their fur sloughs off, and they develop welts. Previously, Capecchi’s team discovered that a mutation in a gene called Hoxb8 caused mice to show signs of chronic anxiety and to groom themselves excessively.

Unexpectedly, they identified that the source of these behaviors was a type of immune cell called microglia. Accounting for only 10% of cells in the brain, microglia had been thought of as the brain’s “trash collectors” that disposed of dying neurons—the most common brain cell—and abnormally shaped proteins.

Their discoveries were also among the first to reveal that Hoxb8 microglia were important for controlling behavior by communicating with specific neuronal circuits. 

But how microglia accomplished these tasks remained a mystery. To learn more, Nagajaran turned to optogenetics, a technique that combines laser light and genetic engineering. Like playing a video game, he used the laser to stimulate specific populations of microglia in the brain.

To the researchers’ amazement, they could turn on anxiety-related behaviors with the flip of a switch. When they used the laser to stimulate one subpopulation, Hoxb8 microglia, the mice became more anxious. When the laser triggered Hoxb8 microglia in other parts of the brain, the mice groomed themselves.

Targeting Hoxb8 microglia in yet another location had multiple effects: the mice’s anxiety increased, they groomed themselves, and they froze, an indicator of fear. Whenever the scientists turned the laser off, the behaviors stopped.

“That was a big surprise for us,” Nagarajan says. “It is conventionally thought that only neurons can generate behaviors. The current findings shed light on a second way that the brain generates behaviors using microglia.”

In fact, stimulating microglia with the laser caused the neurons sitting next to them to fire more strongly, suggesting that the two cell types communicate with one another to drive distinct behaviors.

Further experiments revealed yet another layer of control by a population of microglia that do not express Hoxb8. Stimulating “non-Hoxb8” and Hoxb8 microglia at the same time prevented the onset of anxiety and OCSD-like behaviors.

These results suggested that the two populations of microglia act like a brake and an accelerator. They balance each other out under normal conditions and induce a disease state when the signals are off-balance.

The research shows that location and type of microglia are two characteristics that appear to be important for fine-tuning anxiety and OCSD behaviors. From there, microglia communicate with specific neurons and neural circuits that ultimately control behavior, Capecchi says.

“We want to learn more about the two-way communications between neurons and microglia,” he says.

“We want to know what’s responsible for that.” Defining these interactions in mice could lead to therapeutic targets for controlling excessive anxiety in patients.

About this neuroscience and anxiety research news

Author: Julie Kiefer
Source: University of Utah
Contact: Julie Kiefer – University of Utah
Image: The image is credited to Neuroscience News

Original Research: Open access.
Optogenetic stimulation of mouse Hoxb8 microglia in specific regions of the brain induces anxiety, grooming, or both” by Naveen Nagarajan & Mario R. Capecchi. Molecular Psychiatry


Optogenetic stimulation of mouse Hoxb8 microglia in specific regions of the brain induces anxiety, grooming, or both

Previously, we have shown that either disruption of the Hoxb8 gene or ablation of a microglial subpopulation, Hoxb8 microglia, results in mice exhibiting both chronic anxiety and OCSD-like behavior, compulsive pathological hair pulling (trichotillomania), to the point of showing lesions at the sites of overgrooming.

Herein we show, that optogenetic stimulation of Hoxb8 microglia in specific regions of the brain induces elevated anxiety, grooming or both.

Optogenetic stimulation of Hoxb8 microglia within the dorsomedial striatum (DMS) or the medial prefrontal cortex (mPFC) induces grooming, whereas stimulation of Hoxb8 microglia in the basolateral amygdala (BLA) or central amygdala (CeA) produces elevated anxiety.

Optogenetic stimulation of Hoxb8 microglia in the ventral CA1 region of the hippocampus (vCA1) induces both behaviors as well as freezing. In vitro we directly demonstrate that optogenetic stimulation of Hoxb8 microglia in specific regions of the brain activate neighboring neural activity through the induction of the c-fos-immediate early response.

These experiments connect outputs from optogenetically stimulated Hoxb8 microglia, within specific regions of the brain, to the activation of neurons and neural circuits that in turn enable induction of these behaviors.

These experiments suggest that Hoxb8 microglia are likely to be among, or the main, first responders to signals that evoke these behaviors. The same regions of the brain (DMS, mPFC, BLA, CeA and vCA1) have previously been defined at the neuronal level, by optogenetics, to control anxiety in mice.

Intriguingly, the optogenetic experiments in microglia suggest that the two populations of microglia, canonical non-Hoxb8 and Hoxb8 microglia, function in opposition rather than in parallel to each other, providing a biological reason for the presence of two microglial subpopulations in mice.

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