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Published on: March 17, 2015
MrgprB4 in trigeminal neurons expressing TRPA1 modulates unpleasant sensations
Shota Tobori1, Haruka Hiyama1, Takahito Miyake2
1Department of Molecular Pharmacology, Graduate School of Pharmaceutical Sciences, Kyoto University, 46-29 Yoshida-Shimoadachi-cho, Sakyo-ku, Kyoto 606-8501, Japan.
Abstract:
Gentle touch such as stroking of the skin produces a pleasant feeling, which is detected by a rare subset of sensory neurons that express Mas-related G protein-coupled receptor B4 (MrgprB4) in mice. We examined small populations of MrgprB4-positive neurons in the trigeminal ganglion and the dorsal root ganglion, and most of these were sensitive to transient receptor potential ankyrin 1 (TRPA1) agonist but not TRPV1, TRPM8, or TRPV4 agonists. Deficiency of MrgprB4 did not affect noxious pain or itch behaviors in the hairless plantar and hairy cheek. Although behavior related to acetone-induced cold sensing in the hind paw was not changed, unpleasant sensory behaviors in response to acetone application or sucrose splash to the cheek were significantly enhanced in Mrgprb4-knockout mice as well as in TRPA1-knockout mice. These results suggest that MrgprB4 in the trigeminal neurons produces pleasant sensations in cooperation with TRPA1, rather than noxious or cold sensations. Pleasant sensations may modulate unpleasant sensations on the cheek via MrgprB4.
Insights
Gentle touch sensations are mediated by Mas-related G protein-coupled receptor B4 (MrgprB4) and TRPA1 channels in mice. These receptors enhance pleasant feelings and modulate unpleasant sensations on the cheek.
Area of Science:
- Neuroscience
- Sensory Biology
- Molecular Biology
Background:
- Gentle touch elicits pleasant sensations detected by specific sensory neurons expressing Mas-related G protein-coupled receptor B4 (MrgprB4).
- The precise role of MrgprB4 in sensory processing, particularly in relation to other sensory channels, remains incompletely understood.
Purpose of the Study:
- To investigate the function of MrgprB4-expressing neurons in sensory perception.
- To determine the interaction between MrgprB4 and transient receptor potential (TRP) channels in mediating touch-related sensations.
Main Methods:
- Electrophysiological recordings from MrgprB4-positive neurons in the trigeminal and dorsal root ganglia.
- Behavioral analysis of wild-type, Mrgprb4-knockout, and TRPA1-knockout mice in response to various sensory stimuli (e.g., acetone, sucrose).
Main Results:
- MrgprB4-positive neurons were primarily sensitive to transient receptor potential ankyrin 1 (TRPA1) agonists, not TRPV1, TRPM8, or TRPV4 agonists.
- Mrgprb4-knockout mice exhibited enhanced unpleasant sensory behaviors in response to acetone and sucrose application on the cheek.
- TRPA1-knockout mice also showed heightened unpleasant sensory responses, suggesting a cooperative role with MrgprB4.
Conclusions:
- MrgprB4, in conjunction with TRPA1 in trigeminal neurons, contributes to pleasant sensations rather than noxious or cold sensations.
- Pleasant sensations mediated by MrgprB4 may play a role in modulating unpleasant sensory experiences on the face.
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