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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 4

Fluorescent AGs label lysosomes.

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Fluorescent AGs label lysosomes.
(A) Neo-TR–labeled puncta in exposed HC...
(A) Neo-TR–labeled puncta in exposed HCs also label with lysosomal markers. 5 dpf zebrafish were simultaneously exposed to 50 μM Neo-TR and LysoTracker Green before washout and imaging. Most LysoTracker-positive puncta contain Neo-TR (see yellow arrows as examples). Note that some immature HCs label with LysoTracker but not appreciable Neo-TR (right cell). Scale bar: 5 μm. (B) Neo-TR puncta colocalize with a genetically encoded late endosome/lysosome marker, GFP-Rab7. Transgenic zebrafish ubiquitously expressing GFP-Rab7 were exposed to Neo-TR. Most Neo-TR–positive puncta also have accumulations of GFP-Rab7 (see yellow arrows as examples). Scale bar: 5 μm. (C) Zoom of an intracellular region of an HC with GFP-Rab7/Neo-TR double-labeled puncta. Scale bar: 3 μm. (D) Neo-TR is present in the lumen of lysosomes. In large lysosomes where the outer membrane and lumen can be resolved, GFP-Rab7 marks membranes that surround Neo-TR signal within the lumen. Scale bar: 2 μm. (E) Quantification of overlap of markers with Neo-TR signal in puncta. Neo-BODIPY and GFP-Rab5 show results of markers where there is either near-complete or near-absent overlap (error bars: ± 1 SD). Data taken from 10 neuromasts. ****P < 0.0001 based on Holm-Šidák multiple comparison analysis after Kruskal-Wallis test. (See Figure 1 and Supplemental Figure 3C for representative Neo-BODIPY and GFP-Rab5 images.)

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

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