Evaluation of Cisplatin-Induced Pathology in the Larval Zebrafish Lateral Line

被引:5
作者
Lee, David S. [1 ]
Schrader, Angela [1 ]
Bell, Emily [1 ]
Warchol, Mark E. [1 ,2 ]
Sheets, Lavinia [1 ,3 ]
机构
[1] Washington Univ, Sch Med, Dept Otolaryngol Head & Neck Surg, St Louis, MO 63110 USA
[2] Washington Univ, Dept Neurosci, Sch Med, St Louis, MO 63110 USA
[3] Washington Univ, Dept Dev Biol, Sch Med, St Louis, MO 63110 USA
基金
美国国家卫生研究院;
关键词
cisplatin; ototoxicity; zebrafish; lateral line organ; macrophage; rheotaxis; INDUCED OTOTOXICITY; HAIR-CELLS; MECHANISMS;
D O I
10.3390/ijms232214302
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Cisplatin is an effective anticancer agent, but also causes permanent hearing loss by damaging hair cells-the sensory receptors essential for hearing. There is an urgent clinical need to protect cochlear hair cells in patients undergoing cisplatin chemotherapy. The zebrafish lateral line organ contains hair cells and has been frequently used in studies to screen for otoprotective compounds. However, these studies have employed a wide range of cisplatin dosages and exposure times. We therefore performed a comprehensive evaluation of cisplatin ototoxicity in the zebrafish lateral line with the goal of producing a standardized, clinically relevant protocol for future studies. To define the dose- and time-response patterns of cisplatin-induced hair-cell death, we treated 6-day-old larvae for 2 h in 50 mu M-1 mM cisplatin and allowed them to recover. We observed delayed hair cell death, which peaked at 4-8 h post-exposure. Cisplatin also activated a robust inflammatory response, as determined by macrophage recruitment and phagocytosis of hair cells. However, selective depletion of macrophages did not affect hair cell loss. We also examined the effect of cisplatin treatment on fish behavior and found that cisplatin-induced lateral line injury measurably impaired rheotaxis. Finally, we examined the function of remaining hair cells that appeared resistant to cisplatin treatment. We observed significantly reduced uptake of the cationic dye FM1-43 in these cells relative to untreated controls, indicating that surviving hair cells may be functionally impaired. Cumulatively, these results indicate that relatively brief exposures to cisplatin can produce hair cell damage and delayed hair cell death. Our observations provide guidance on standardizing methods for the use of the zebrafish model in studies of cisplatin ototoxicity.
引用
收藏
页数:15
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