Single-molecule fluorescence microscopy reveals regulatory mechanisms of MYO7A-driven cargo transport in stereocilia of live inner ear hair cells

Stereocilia are F-actin-based cylindrical protrusions on the apical surface of inner ear hair cells that function as biological mechanosensors of sound and acceleration. During stereocilia development, specific unconventional myosins transport proteins and phospholipids as cargo and mediate elongation, differentiation and acquisition of the mechanoelectrical transduction (MET). How unconventional myosins localize themselves and cargo in stereocilia using energy from ATP hydrolysis is only partially understood. Here, we developed STELLA-SPIM microscopy to visualize movement of single myosin molecules in live hair cell stereocilia. STELLA-SPIM demonstrated that MYO7A, a component of MET machinery, shows processive movement toward stereocilia tips when chemically dimerized or constitutively activated by missense mutations disabling tail-mediated autoinhibition. Conversely, MYO7A shows step-wise but not processive movement in stereocilia when its tail is tethered to the plasma membrane or F-actin in the presence of MYO7A interacting partners. We posit that MYO7A dimerizes and moves processively in stereocilia when unleashed from autoinhibition.

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Journal
Nature Communications
Published
2025-09-01
DOI
https://doi.org/10.1038/s41467-025-63102-0
Primary Topic
Hearing, Cochlea, Tinnitus, Genetics
Type
article
Field-Weighted Citation Impact
0.00

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article

Single-molecule fluorescence microscopy reveals regulatory mechanisms of MYO7A-driven cargo transport in stereocilia of live inner ear hair cells

Thomas B. Friedman, Samuel Mawuli Adadey, Takushi Miyoshi, Harshad D. Vishwasrao et al.
Nature Communications
Hearing, Cochlea, Tinnitus, Genetics
article

Single-molecule fluorescence microscopy reveals regulatory mechanisms of MYO7A-driven cargo transport in stereocilia of live inner ear hair cells

Thomas B. Friedman, Samuel Mawuli Adadey, Takushi Miyoshi, Harshad D. Vishwasrao, Narinobu Harada, Hari Shroff, Yasuko Ishibashi, Inna A. Belyantseva, Mrudhula Sajeevadathan, Junko Miyoshi
article en

Abstract

Stereocilia are F-actin-based cylindrical protrusions on the apical surface of inner ear hair cells that function as biological mechanosensors of sound and acceleration. During stereocilia development, specific unconventional myosins transport proteins and phospholipids as cargo and mediate elongation, differentiation and acquisition of the mechanoelectrical transduction (MET). How unconventional myosins localize themselves and cargo in stereocilia using energy from ATP hydrolysis is only partially understood. Here, we developed STELLA-SPIM microscopy to visualize movement of single myosin molecules in live hair cell stereocilia. STELLA-SPIM demonstrated that MYO7A, a component of MET machinery, shows processive movement toward stereocilia tips when chemically dimerized or constitutively activated by missense mutations disabling tail-mediated autoinhibition. Conversely, MYO7A shows step-wise but not processive movement in stereocilia when its tail is tethered to the plasma membrane or F-actin in the presence of MYO7A interacting partners. We posit that MYO7A dimerizes and moves processively in stereocilia when unleashed from autoinhibition.

Nature CommunicationsVol. 16(1)
Southern Illinois University Carbondale (US), National Institutes of Health (US), Howard Hughes Medical Institute (US), Janelia Research Campus (US), Southern Illinois University School of Medicine (US), National Institute of Biomedical Imaging and Bioengineering (US), Osaka Nishi Clinic (JP), National Institute on Deafness and Other Communication Disorders (US)
Howard Hughes Medical Institute, School of Medicine, Southern Illinois University, Japan Society for the Promotion of Science, National Institute on Deafness and Other Communication Disorders, National Institute of Biomedical Imaging and Bioengineering
Openalex Percentile: Top 78%
Hearing, Cochlea, Tinnitus, Genetics
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