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Fluorescent aminoglycosides reveal intracellular trafficking routes in mechanosensory hair cells
Dale W. Hailey, Robert Esterberg, Tor H. Linbo, Edwin W. Rubel, David W. Raible
Dale W. Hailey, Robert Esterberg, Tor H. Linbo, Edwin W. Rubel, David W. Raible
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Research Article Cell biology

Fluorescent aminoglycosides reveal intracellular trafficking routes in mechanosensory hair cells

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Abstract

Aminoglycosides (AGs) are broad-spectrum antibiotics that are associated with kidney damage, balance disorders, and permanent hearing loss. This damage occurs primarily by killing of proximal tubule kidney cells and mechanosensory hair cells, though the mechanisms underlying cell death are not clear. Imaging molecules of interest in living cells can elucidate how molecules enter cells, traverse intracellular compartments, and interact with sites of activity. Here, we have imaged fluorescently labeled AGs in live zebrafish mechanosensory hair cells. We determined that AGs enter hair cells via both nonendocytic and endocytic pathways. Both routes deliver AGs from the extracellular space to lysosomes, and structural differences between AGs alter the efficiency of this delivery. AGs with slower delivery to lysosomes were immediately toxic to hair cells, and impeding lysosome delivery increased AG-induced death. Therefore, pro-death cascades induced at early time points of AG exposure do not appear to derive from the lysosome. Our findings help clarify how AGs induce hair cell death and reveal properties that predict toxicity. Establishing signatures for AG toxicity may enable more efficient evaluation of AG treatment paradigms and structural modifications to reduce hair cell damage. Further, this work demonstrates how following fluorescently labeled drugs at high resolution in living cells can reveal important details about how drugs of interest behave.

Authors

Dale W. Hailey, Robert Esterberg, Tor H. Linbo, Edwin W. Rubel, David W. Raible

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Figure 2

Fluorescent neomycin preferentially enters and kills LL HCs.

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Fluorescent neomycin preferentially enters and kills LL HCs.
(A) A neuro...
(A) A neuromast in a sedated 5 days post fertilization (dpf) zebrafish imaged during chronic exposure to 50 μM Neo-TR. Neo-TR was added to the media at time 0. Neo-TR first enters the kinocilia and stereocilia (6 minutes) and subsequently the HC body in both puncta (yellow arrows) and diffuse pools (9 minutes 30 seconds). Note that non-HCs in the fish do not take up Neo-TR. HCs with high concentrations of Neo-TR show blebbing at the apical region and kinocilia (asterisks: 21 minutes 30 seconds; 28 minutes), and separation of the apical region from the HC body (bracket: 21 minutes 30 seconds). (See also Supplemental Video 3.) Scale bar: 10 μm. (B) Neo-TR time series in a brn3c-GFP transgenic zebrafish, treated as in A. The appearance of Neo-TR on the stereocilia (plus symbol) and kinocilia (asterisk) occurs nearly simultaneously and prior to detectable Neo-TR throughout the HC body (yellow arrow). Scale bar: 10 μm. (See also Supplemental Video 3.)

Copyright © 2026 American Society for Clinical Investigation
ISSN: 0021-9738 (print), 1558-8238 (online)

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