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      Neomycin-induced hair cell death and rapid regeneration in the lateral line of zebrafish (Danio rerio).

      JARO: Journal of the Association for Research in Otolaryngology
      Acetylation, Actins, metabolism, Animals, Bromodeoxyuridine, Cell Death, Coloring Agents, Dose-Response Relationship, Drug, Hair Cells, Auditory, drug effects, physiology, ultrastructure, Larva, Microscopy, Electron, Scanning, Neomycin, administration & dosage, poisoning, Phalloidine, Pyridinium Compounds, Regeneration, Staining and Labeling, Tubulin, Zebrafish, growth & development

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          Abstract

          Mechanoreceptive hair cells are extremely sensitive to aminoglycoside antibiotics, including neomycin. Hair cell survival was assessed in larval wild-type zebrafish lateral line neuromasts 4 h after initial exposure to a range of neomycin concentrations for 1 h. Each of the lateral line neuromasts was scored in live fish for the presence or absence of hair cells using the fluorescent vital dye DASPEI to selectively label hair cells. All neuromasts were devoid of DASPEI-labeled hair cells 4 h after 500 microM neomycin exposure. Vital DASPEI staining was proportional to the number of hair cells per neuromast identified in fixed larvae using immunocytochemistry for acetylated tubulin and phalloidin labeling. The time course of hair cell regeneration in the lateral line neuromasts was also analyzed following neomycin-induced damage. Regenerated hair cells were first observed using live DASPEI staining 12 and 24 h following neomycin treatment. The potential role of proliferation in regenerating hair cells was analyzed. A 1 h pulse-fix protocol using bromodeoxyuridine (BrdU) incorporation was used to identify S-phase cells in neuromasts. BrdU incorporation in neomycin-damaged neuromasts did not differ from control neuromasts 4 h after drug exposure but was dramatically upregulated after 12 h. The proliferative cells identified during a 1 h period at 12 h after neomycin treatment were able to give rise to new hair cells by 24-48 h after drug treatment. The results presented here provide a standardized preparation for studying and identifying genes that influence vertebrate hair cell death, survival, and regeneration following ototoxic insults.

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