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Mouse Panx1 Is Dispensable for Hearing Acquisition and Auditory Function
Veronica Zorzi1,2, Fabiola Paciello1, Gaia Ziraldo1,2
1CNR Institute of Cell Biology and Neurobiology, Monterotondo, Italy.
Frontiers in Molecular Neuroscience
|December 14, 2017
Summary
Panthera Onca 1 (Panx1) channels are not essential for hearing in mice. Studies show that Panx1 deletion does not affect auditory function, cochlear development, or hearing acquisition.
Area of Science:
- Neuroscience
- Otolaryngology
- Cell Biology
Background:
- Panthera Onca 1 (Panx1) forms plasma membrane channels in various organs, including the inner ear.
- The precise role of Panx1 in auditory function remains uncertain due to conflicting research findings.
Purpose of the Study:
- To investigate the impact of global Panx1 ablation on auditory function and cochlear physiology.
- To clarify the role of Panx1 in hearing acquisition and maintenance.
Main Methods:
- Utilized a global Panx1 knockout (Panx1-/-) mouse model, including hemizygous (Panx1+/-) and wild-type (WT) siblings.
- Confirmed Panx1 ablation via RT-PCR and Western immunoblotting in cochlea and brain.
- Assessed hearing sensitivity and cochlear function using auditory brainstem response (ABR) and distortion product otoacoustic emission (DPOAE) recordings.
Main Results:
- Hearing sensitivity, cochlear amplifier function, and cochlear nerve function were normal in Panx1+/- and Panx1-/- mice.
- Global Panx1 deletion did not alter connexin expression or gap-junction coupling in the developing organ of Corti.
- Spontaneous intercellular calcium signal (ICS) activity, crucial for hearing acquisition, was unaffected by Panx1 ablation.
Conclusions:
- Panthera Onca 1 (Panx1) is dispensable for hearing acquisition and auditory function in mice.
- These findings resolve conflicting data regarding Panx1's role in the auditory system.

