critical self-tuning and efferent control of inner ear hair cells
ORAL
Abstract
Hair cells employ active mechanisms to improve their sensitivity to force stimuli. A plethora of measurements indicate that these mechanisms position hair bundles, the mechanosensory organelles of hair cells, near a Hopf bifurcation. The recent disovery that the self-oscillations that embody these mechanisms are suppressed by powerful stimuli corroborates a normal form model for hair bundle dynamics in which a self-tuning process robustly maintains the control parameter in the proximity of the critical point.
Synaptic input to hair cells inhibits self-oscillations but negates the stimulus-induced suppression effect; inspired by the observation of this subtle latter phenomenon, we show that synaptic input can be understood as a distinct process governing the control parameter, and we explore the effects of synaptic input and critical self-tuning on the response of hair bundles to forcing.
Synaptic input to hair cells inhibits self-oscillations but negates the stimulus-induced suppression effect; inspired by the observation of this subtle latter phenomenon, we show that synaptic input can be understood as a distinct process governing the control parameter, and we explore the effects of synaptic input and critical self-tuning on the response of hair bundles to forcing.
*This work was funded in part by the National Science Foundation Physics of Living Systems under grant 2210316 and in part by the Air Force Office of Scientific Research under grant FA9550-23-1-0713.
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Publication: DOI: 10.1016/j.bpj.2024.09.006
Presenters
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Charles Metzler-Winslow
- University of California, Los Angeles