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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 10

Inhibiting MET activity decreases the rate of AG loading into HCs, increases the relative amount of AGs delivered to lysosomes, and protects HCs from AG exposure.

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Inhibiting MET activity decreases the rate of AG loading into HCs, incre...
(A) Benzamil, an inhibitor of MET, impedes entry of Neo-TR into HCs in a dose-dependent manner. Zebrafish were pre-exposed for 5 minutes to indicated concentrations of benzamil, and then cotreated with 50 μM Neo-TR for 5 minutes, washed, and imaged. Neo-TR signal was quantified as described in Figure 3A. (B) Treatment with benzamil also impedes FM1-43 entry into HCs in a dose-dependent manner, similarly to its analog amiloride, shown in Figure 3B, and consistent with its activity as a MET inhibitor. (C) The relative amount of Neo-TR loaded into lysosomes increases with increasing benzamil concentrations. Loading of Neo-TR into lysosomes was assayed as described in Figure 5C. (D) This same range of benzamil concentrations shows an increasing degree of HC protection from a 1-hour, 200-μM neomycin exposure. HC survival was assessed as described in Figure 1. Error bars: ± 1 SD. Each graphed symbol represents 1 fish, 5 neuromasts per fish.

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

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