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Updated: Feb 16, 2026

Generation and Culture of Lingual Organoids Derived from Adult Mouse Taste Stem Cells
Published on: April 5, 2021
TRPM4 and TRPM5 are both required for normal signaling in taste receptor cells
Debarghya Dutta Banik1, Laura E Martin2, Marc Freichel3
1Department of Biological Sciences, University at Buffalo, Buffalo, NY 14260.
Abstract:
Peripheral taste receptor cells use multiple signaling pathways to transduce taste stimuli into output signals that are sent to the brain. Transient receptor potential melastatin 5 (TRPM5), a sodium-selective TRP channel, functions as a common downstream component in sweet, bitter, and umami signaling pathways. In the absence of TRPM5, mice have a reduced, but not abolished, ability to detect stimuli, suggesting that a TRPM5-independent pathway also contributes to these signals. Here, we identify a critical role for the sodium-selective TRP channel TRPM4 in taste transduction. Using live cell imaging and behavioral studies in KO mice, we show that TRPM4 and TRPM5 are both involved in taste-evoked signaling. Loss of either channel significantly impairs taste, and loss of both channels completely abolishes the ability to detect bitter, sweet, or umami stimuli. Thus, both TRPM4 and TRPM5 are required for transduction of taste stimuli.
Insights
Transient receptor potential melastatin 5 (TRPM5) and TRPM4 channels are crucial for taste. This study shows both TRPM4 and TRPM5 are essential for detecting sweet, bitter, and umami tastes, with double knockout mice showing no taste ability.
Area of Science:
- Neuroscience
- Sensory Biology
- Molecular Biology
Background:
- Peripheral taste receptor cells utilize complex signaling pathways for taste transduction.
- Transient receptor potential melastatin 5 (TRPM5), a sodium-selective TRP channel, is a known downstream element in sweet, bitter, and umami taste signaling.
- Previous research indicated a TRPM5-independent pathway contributes to taste perception, suggesting other channels are involved.
Purpose of the Study:
- To investigate the role of Transient receptor potential melastatin 4 (TRPM4) in taste transduction.
- To elucidate the combined function of TRPM4 and TRPM5 in taste signaling pathways.
Main Methods:
- Utilized live cell imaging techniques to observe taste-evoked signaling.
- Conducted behavioral studies using knockout (KO) mice lacking TRPM4 and/or TRPM5.
- Analyzed the impact of channel deficiencies on taste detection.
Main Results:
- Identified a critical role for the sodium-selective TRP channel TRPM4 in taste transduction.
- Demonstrated that both TRPM4 and TRPM5 are involved in taste-evoked signaling.
- Showed that loss of either TRPM4 or TRPM5 significantly impairs taste perception in mice.
- Confirmed that the complete absence of both TRPM4 and TRPM5 abolishes the ability to detect sweet, bitter, and umami stimuli.
Conclusions:
- Both TRPM4 and TRPM5 channels are essential and required for the transduction of sweet, bitter, and umami taste stimuli.
- These findings highlight the synergistic role of TRPM4 and TRPM5 in mammalian taste perception.
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