Ashley Scott Patterson, Joseph Dugdale, Alaa Koleilat, Anna Krauss, Gabriel A Hernandez-Herrera, Jasmine G Wallace, Cassidy Petree, Gaurav K Varshney, Lisa A Schimmenti
{"title":"YO-PRO-1和DASPEI的重要染料吸收取决于斑马鱼毛细胞的机电传导功能","authors":"Ashley Scott Patterson, Joseph Dugdale, Alaa Koleilat, Anna Krauss, Gabriel A Hernandez-Herrera, Jasmine G Wallace, Cassidy Petree, Gaurav K Varshney, Lisa A Schimmenti","doi":"10.1007/s10162-024-00967-w","DOIUrl":null,"url":null,"abstract":"<p><strong>Purpose: </strong>Vital dyes allow the visualization of cells in vivo without causing tissue damage, making them a useful tool for studying lateral line and inner ear hair cells in living zebrafish and other vertebrates. FM1-43, YO-PRO-1, and DASPEI are three vital dyes commonly used for hair cell visualization. While it has been established that FM1-43 enters hair cells of zebrafish and other organisms through the mechanoelectrical transduction (MET) channel, the mechanism of entry into hair cells for YO-PRO-1 and DASPEI has not been established despite widespread use. We hypothesize that YO-PRO-1 and DASPEI entry into zebrafish hair cells is MET channel uptake dependent similar to FM1-43.</p><p><strong>Methods: </strong>To test this hypothesis, we used both genetic and pharmacologic means to block MET channel function. Genetic based MET channel assays were conducted with two different mechanotransduction defective zebrafish lines, specifically the myo7aa<sup>-/-</sup> loss of function mutant tc320b (p.Y846X) and cdh23<sup>-/-</sup> loss of function mutant (c.570-571del). Pharmacologic assays were performed with Gadolinium(III) Chloride (Gad(III)), a compound that can temporarily block mechanotransduction activity.</p><p><strong>Results: </strong>Five-day post fertilization (5dpf) myo7aa<sup>-/-</sup> and cdh23<sup>-/-</sup> larvae incubated with FM1-43, YO-PRO-1, and DASPEI all showed nearly absent uptake of each vital dye. Treatment of wildtype zebrafish larvae with Gad(III) significantly reduces uptake of FM1-43, YO-PRO-1, and DASPEI vital dyes.</p><p><strong>Conclusion: </strong>These results indicate that YO-PRO-1 and DASPEI entry into zebrafish hair cells is MET channel dependent similar to FM1-43. This knowledge expands the repertoire of vital dyes that can be used to assess mechanotransduction and MET channel function in zebrafish and other vertebrate models of hair cell function.</p>","PeriodicalId":56283,"journal":{"name":"Jaro-Journal of the Association for Research in Otolaryngology","volume":" ","pages":"531-543"},"PeriodicalIF":2.4000,"publicationDate":"2024-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11683040/pdf/","citationCount":"0","resultStr":"{\"title\":\"Vital Dye Uptake of YO-PRO-1 and DASPEI Depends Upon Mechanoelectrical Transduction Function in Zebrafish Hair Cells.\",\"authors\":\"Ashley Scott Patterson, Joseph Dugdale, Alaa Koleilat, Anna Krauss, Gabriel A Hernandez-Herrera, Jasmine G Wallace, Cassidy Petree, Gaurav K Varshney, Lisa A Schimmenti\",\"doi\":\"10.1007/s10162-024-00967-w\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Purpose: </strong>Vital dyes allow the visualization of cells in vivo without causing tissue damage, making them a useful tool for studying lateral line and inner ear hair cells in living zebrafish and other vertebrates. FM1-43, YO-PRO-1, and DASPEI are three vital dyes commonly used for hair cell visualization. While it has been established that FM1-43 enters hair cells of zebrafish and other organisms through the mechanoelectrical transduction (MET) channel, the mechanism of entry into hair cells for YO-PRO-1 and DASPEI has not been established despite widespread use. We hypothesize that YO-PRO-1 and DASPEI entry into zebrafish hair cells is MET channel uptake dependent similar to FM1-43.</p><p><strong>Methods: </strong>To test this hypothesis, we used both genetic and pharmacologic means to block MET channel function. Genetic based MET channel assays were conducted with two different mechanotransduction defective zebrafish lines, specifically the myo7aa<sup>-/-</sup> loss of function mutant tc320b (p.Y846X) and cdh23<sup>-/-</sup> loss of function mutant (c.570-571del). Pharmacologic assays were performed with Gadolinium(III) Chloride (Gad(III)), a compound that can temporarily block mechanotransduction activity.</p><p><strong>Results: </strong>Five-day post fertilization (5dpf) myo7aa<sup>-/-</sup> and cdh23<sup>-/-</sup> larvae incubated with FM1-43, YO-PRO-1, and DASPEI all showed nearly absent uptake of each vital dye. Treatment of wildtype zebrafish larvae with Gad(III) significantly reduces uptake of FM1-43, YO-PRO-1, and DASPEI vital dyes.</p><p><strong>Conclusion: </strong>These results indicate that YO-PRO-1 and DASPEI entry into zebrafish hair cells is MET channel dependent similar to FM1-43. 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引用次数: 0
摘要
目的:活力染料可使活体细胞可视化而不会造成组织损伤,是研究活体斑马鱼和其他脊椎动物侧线和内耳毛细胞的有用工具。FM1-43、YO-PRO-1 和 DASPEI 是常用于观察毛细胞的三种重要染料。虽然已经确定 FM1-43 通过机械电转导(MET)通道进入斑马鱼和其他生物的毛细胞,但 YO-PRO-1 和 DASPEI 进入毛细胞的机制尚未确定,尽管它们已被广泛使用。我们假设 YO-PRO-1 和 DASPEI 进入斑马鱼毛细胞与 FM1-43 类似,都依赖于 MET 通道的摄取:为了验证这一假设,我们采用了基因和药物方法来阻断 MET 通道的功能。我们用两种不同的机械传导缺陷斑马鱼品系,特别是 myo7aa-/- 功能缺失突变体 tc320b(p.Y846X)和 cdh23-/- 功能缺失突变体(c.570-571del)进行了基于基因的 MET 通道检测。用氯化钆(III)(Gad(III))进行了药理学检测,该化合物可暂时阻断机械传导活性:结果:受精后五天(5dpf)的myo7aa-/-和cdh23-/-幼体在与FM1-43、YO-PRO-1和DASPEI一起孵育时,对每种重要染料的吸收都几乎为零。用 Gad(III)处理野生型斑马鱼幼体可显著减少对 FM1-43、YO-PRO-1 和 DASPEI 生命染料的吸收:这些结果表明,YO-PRO-1 和 DASPEI 进入斑马鱼毛细胞与 FM1-43 类似,都依赖于 MET 通道。这一知识扩展了可用于评估斑马鱼和其他脊椎动物毛细胞功能模型中机械传导和 MET 通道功能的重要染料的范围。
Vital Dye Uptake of YO-PRO-1 and DASPEI Depends Upon Mechanoelectrical Transduction Function in Zebrafish Hair Cells.
Purpose: Vital dyes allow the visualization of cells in vivo without causing tissue damage, making them a useful tool for studying lateral line and inner ear hair cells in living zebrafish and other vertebrates. FM1-43, YO-PRO-1, and DASPEI are three vital dyes commonly used for hair cell visualization. While it has been established that FM1-43 enters hair cells of zebrafish and other organisms through the mechanoelectrical transduction (MET) channel, the mechanism of entry into hair cells for YO-PRO-1 and DASPEI has not been established despite widespread use. We hypothesize that YO-PRO-1 and DASPEI entry into zebrafish hair cells is MET channel uptake dependent similar to FM1-43.
Methods: To test this hypothesis, we used both genetic and pharmacologic means to block MET channel function. Genetic based MET channel assays were conducted with two different mechanotransduction defective zebrafish lines, specifically the myo7aa-/- loss of function mutant tc320b (p.Y846X) and cdh23-/- loss of function mutant (c.570-571del). Pharmacologic assays were performed with Gadolinium(III) Chloride (Gad(III)), a compound that can temporarily block mechanotransduction activity.
Results: Five-day post fertilization (5dpf) myo7aa-/- and cdh23-/- larvae incubated with FM1-43, YO-PRO-1, and DASPEI all showed nearly absent uptake of each vital dye. Treatment of wildtype zebrafish larvae with Gad(III) significantly reduces uptake of FM1-43, YO-PRO-1, and DASPEI vital dyes.
Conclusion: These results indicate that YO-PRO-1 and DASPEI entry into zebrafish hair cells is MET channel dependent similar to FM1-43. This knowledge expands the repertoire of vital dyes that can be used to assess mechanotransduction and MET channel function in zebrafish and other vertebrate models of hair cell function.
期刊介绍:
JARO is a peer-reviewed journal that publishes research findings from disciplines related to otolaryngology and communications sciences, including hearing, balance, speech and voice. JARO welcomes submissions describing experimental research that investigates the mechanisms underlying problems of basic and/or clinical significance.
Authors are encouraged to familiarize themselves with the kinds of papers carried by JARO by looking at past issues. Clinical case studies and pharmaceutical screens are not likely to be considered unless they reveal underlying mechanisms. Methods papers are not encouraged unless they include significant new findings as well. Reviews will be published at the discretion of the editorial board; consult the editor-in-chief before submitting.