The mechanosensitive channel TMEM63B contributes to noxious heat sensation in the dorsal root ganglia

In mammals, heat sensation is primarily mediated by thermosensitive channels, particularly transient receptor potential (TRP) channels, in dorsal root ganglion (DRG) neurons. However, whether additional channels contribute to noxious heat detection remains unclear. Here, we investigated the role of the mechanosensitive cation channel TMEM63B in DRG neurons and unexpectedly discovered its involvement in noxious thermosensation rather than mechanosensation. TMEM63B was broadly expressed in DRG neurons, and its global knockout or DRG-specific conditional knockout markedly reduced heat sensitivity. Deletion of TMEM63B significantly attenuated heat-induced calcium responses and currents in DRG neurons and elevated the temperature threshold for action potential initiation. Recombinant TMEM63B exhibited moderate heat response in calcium imaging assays. Notably, in the presence of arachidonic acid, TMEM63B was strongly activated by heat, suggesting that its thermosensitivity is modulated by the membrane lipid environment. Together, these findings identify TMEM63B as a novel channel contributing to heat sensation and reveal a lipid-dependent modulation of its channel activity.

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Publication Details

Journal
PLoS Biology
Published
2026-10-16
DOI
https://doi.org/10.1371/journal.pbio.3004060
Primary Topic
Ion Channels and Receptors
Type
article
Field-Weighted Citation Impact
0.00

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article

The mechanosensitive channel TMEM63B contributes to noxious heat sensation in the dorsal root ganglia

Guifang Duan, Tianjiao Xia, Yun Stone Shi, Dan Wang et al.
PLoS Biology
Ion Channels and Receptors
article

The mechanosensitive channel TMEM63B contributes to noxious heat sensation in the dorsal root ganglia

Guifang Duan, Tianjiao Xia, Yun Stone Shi, Dan Wang, Yan‐Yu Zang, Changlin Li, Yun Xu, Dan Wu, Jiang Chen, Xiaoping Gu, Chang Ye
article en

Abstract

In mammals, heat sensation is primarily mediated by thermosensitive channels, particularly transient receptor potential (TRP) channels, in dorsal root ganglion (DRG) neurons. However, whether additional channels contribute to noxious heat detection remains unclear. Here, we investigated the role of the mechanosensitive cation channel TMEM63B in DRG neurons and unexpectedly discovered its involvement in noxious thermosensation rather than mechanosensation. TMEM63B was broadly expressed in DRG neurons, and its global knockout or DRG-specific conditional knockout markedly reduced heat sensitivity. Deletion of TMEM63B significantly attenuated heat-induced calcium responses and currents in DRG neurons and elevated the temperature threshold for action potential initiation. Recombinant TMEM63B exhibited moderate heat response in calcium imaging assays. Notably, in the presence of arachidonic acid, TMEM63B was strongly activated by heat, suggesting that its thermosensitivity is modulated by the membrane lipid environment. Together, these findings identify TMEM63B as a novel channel contributing to heat sensation and reveal a lipid-dependent modulation of its channel activity.

PLoS BiologyVol. 24(10)
Peking University (CN), Nanjing Drum Tower Hospital (CN), Model Animal Research Center (CN), Guangdong Institute of Intelligence Science and Technology (CN), Nanjing University (CN)
National Natural Science Foundation of China, Natural Science Foundation of Jiangsu Province, National Key Research and Development Program of China, Fundamental Research Funds for the Central Universities, Special Fund Project for Science and Technology Innovation Strategy of Guangdong Province
Openalex Percentile: Top 16%
Ion Channels and Receptors
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