Article Highlight | 10-May-2022

Breathtaking solution for a breathless problem

Protein expression in mouse brain stimulates breathing in oxygen-deprived mice

Kyoto University

Kyoto, Japan -- A drop in oxygen levels, even when temporary, can be critical to brain cells. This explains why the brain is equipped with oxygen sensors. Researchers from Japan and the United States report finding a new oxygen sensor in the mouse brain. 

Cells begin to die in oxygen-deprived conditions, with the biggest oxygen consumers -- such as the cells in the brain -- being the first to go. In response, the brain must respond quickly to force the body to breathe more.

Astrocytes, supporting cells which in part modulate the activity of neurons responsible for breathing, respond to low oxygen levels by highly expressing the protein TRPA1. When there is not enough oxygen in the brain, this expression on the surface of astrocytes induces the secretion of gliotransmitters that cause the neuronal modulation for breathing. 

"Much research in the last decade has indicated that astrocytes act as oxygen sensors, but we know very little about the actual molecular changes that take place," explains corresponding author Yasuo Mori. 

Although astrocytes are located in the central nervous system, they differ from neurons in that they respond to neuronal injury and provide a support system for neurons and synaptic connections.

"We previously found that TRPA1 proteins can sense hypoxia and hyperoxia in peripheral neurons," Mori continues, explaining the team's decision to probe whether they perform a similar function in astrocytes. 

"Interestingly, the sequestering of TRPA1 can only occur in the presence of oxygen at normal or surplus levels; in hypoxia, prolyl hydroxylase activity is suppressed, and TRPA1 is expressed on the astrocyte surface, not in the cytoplasm." 

Once at the plasma membrane, TRPA1 allows the astrocytes to accumulate calcium ions, causing the cells to secreteATP, thereby modulating respiratory neurons. This has been shown to help more mice breathe. 

Once oxygen levels recover, so too does prolyl hydroxylase, returning TRPA1 from the membrane to the cytoplasm.

"While the functions of brain cells seem to depend on their locations in the brain, we note that other brain cells will use different mechanisms to recover oxygen," concludes Nakao.


The paper "O2-Dependent Protein Internalization Underlies Astrocytic Sensing of Acute Hypoxia by Restricting Multimodal TRPA1 Channel Responses" appeared on 16 July 2020 in Current Biology, with doi: 10.1016/j.cub.2020.06.047

About Kyoto University

Kyoto University is one of Japan and Asia's premier research institutions, founded in 1897 and responsible for producing numerous Nobel laureates and winners of other prestigious international prizes. A broad curriculum across the arts and sciences at both undergraduate and graduate levels is complemented by numerous research centers, as well as facilities and offices around Japan and the world. For more information please see:

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