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Fluorescent aminoglycosides reveal intracellular trafficking routes in mechanosensory hair cells
Dale W. Hailey, … , Edwin W. Rubel, David W. Raible
Dale W. Hailey, … , Edwin W. Rubel, David W. Raible
Published December 19, 2016
Citation Information: J Clin Invest. 2017;127(2):472-486. https://doi.org/10.1172/JCI85052.
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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 5

Labeled AGs transit from the diffuse intracellular pool into lysosomes.

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Labeled AGs transit from the diffuse intracellular pool into lysosomes.
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(A) Time-lapse imaging of Neo-TR in pulse-labeled HCs shows a progressive accumulation of Neo-TR in puncta and loss of diffuse signal in the cytosol. Redistribution is apparent within 20 minutes of exposure. Scale bar: 5 μm. (See also Supplemental Video 4.) (B) Total intracellular Neo-TR fluorescence following pulse exposure does not decrease, indicating that loss of Neo-TR signal from the cytosol is likely due to redistribution to lysosomes and not export from cells. NM, neuromast. (C) An example of image masks (in blue) used to monitor the lysosomal and cytosolic fractions of Neo-TR. Image captured immediately after Neo-TR exposure. Scale bar: 5 μm. (D) Neo-TR added 30 minutes after Neo-BODIPY pulse exposure accumulates in the Neo-BODIPY–prelabeled structures. Image captured 10 minutes after Neo-TR exposure. Scale bar: 5 μm. (E) Quantification of loading into lysosomes following a Neo-TR pulse. After 30 minutes, intensity within the lysosomal mask is approximately 5-fold higher than intensity in the cytosol. Each graphed symbol represents 1 fish, 3 neuromasts per fish. Error bars: ± 1 SD. Flp, Fluorescence in puncta; Fld, diffuse fluorescence.

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ISSN: 0021-9738 (print), 1558-8238 (online)

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