笔者要感谢马修·凯利，蒂齐阿纳Cogliati，杰西卡Gumerson，乌韦·沃尔夫鲁姆，Rivka Levron，中提琴克雷奇默尔和Zoe曼和手稿其关键的评价。这项工作是由Sofja Kovalevskaya奖（与洪堡基金会）和约翰内斯 - 古腾堡大学，美因茨，德国资助。

使用和实施安乐死的动物都按照制度和政府的指导方针和规定，通过CO 2吸入和颈椎脱位最常见。 1.试剂的制备注:在开始时，准备使用分析纯化学药品所有试剂。使用蒸馏水分子级和去离子水，除非另有说明的解决方案。 <ol><li>磷酸盐缓冲盐水（1×PBS）中:通过在1升的H 2 O中溶解8克氯化钠，0.2克氯化钾，1.44克的 Na 2 HPO 4和0.24克KH 2 PO 4使1升1×PBS中的将pH调节至7.4，用HCl。 PBS不需要是无菌的并且可以储存在室温。请注意，此缓冲器被无CaCl 2或MgCl 2的制作。 </li><li>多聚甲醛（4％PFA）:在通风橱准备PFA的4％溶液在1×PBS中。添加多聚甲醛粉40克，以1升1X PBS的。溶解，搅拌并加热至约60℃，慢慢地添加氢氧化钠逐滴提高pH值。一旦粉末溶解，调整pH到7.4，用HCl。通过0.45微米过滤器过滤，并冷冻等分试样。除霜每个实验新鲜等分试样。 </li><li>三硝基甲苯缓冲液:准备的0.1M的Tris-HCl（pH值7.5），0.15 M氯化钠，0.1％的Triton X-100溶液在1升0.1M的Tris-HCl（pH7.5）中溶解8.77克NaCl。加入1 ml的Triton X-100。搅拌使之溶解。商店的Triton缓冲在室温。 </li><li> TRITON模块:加入1 ml山羊血清到9毫升三硝基甲苯缓冲准备10％山羊血清中的Triton缓冲。保存在4℃。如果使用在小鼠升高初级抗体，以1比200稀释到的Triton块的分块步骤添加山羊抗小鼠IgG Fab片段。 注意:如果计划使用扫描电子显微镜（SEM）的样品，下面列出制备另外的试剂。 </li><li>的Hanks&#39;平衡盐溶液（HBSS）与钙和镁:通过从原液稀释制作的HBSS 1倍溶液在无菌蒸馏水H 2 O作为HBSS缓冲液是复杂的制造和有风险，最好是订购预制10X储液。 HBBS缓冲常规使用的最终浓度如下:1.26毫米氯化钙2，0.49毫MgCl 2的-6H2O，0.41毫硫酸镁 -7H2O，5.33毫米氯化钾，0.44毫KH 2 PO 4，4.17毫碳酸氢钠 ，137.93毫摩尔NaCl ，0.34毫的 Na 2 HPO 4，5.56毫摩尔葡萄糖。 </li><li> Hepes缓冲液:准备在1×HBSS的0.1M HEPES溶液中，通过在1升1×HBSS缓冲液中溶解23.8克HEPES。 </li><li>扫描电子显微镜的固定剂（SEM修复）:通过在Hepes缓冲液稀释电子显微镜级戊二醛（2.5％）和多聚甲醛（4％）准备固定剂用于SEM。添加氯化钙 2至10mM的终浓度。 </li><li> 1％四氧化锇（OSO 4）在Hepes缓冲液; 1％四氧化锇在水中的稀释:四氧化锇在Hepes缓冲液的储备液，并separatel中的Y无菌蒸馏水2 O，以1％的终浓度。四氧化锇是剧毒，是最常见的为4％的溶液出售。 </li><li> 1％（重量/体积）单宁酸:将0.5克鞣酸在50ml无菌蒸馏水H 2 O过滤器通过一个0.45孔径过滤器过滤消毒。 </li><li>梯度乙醇溶液系列稀释:用无菌蒸馏水2 O 200标准乙醇在30，50，70，90和95％的乙醇溶液。对于最后的乙醇漂洗，需要100％的乙醇200证明。使用的200度乙醇刚刚打开一瓶最后冲洗。 </li></ol> 2.组织的选择<ol><li>理想情况下，检查胚胎16.5天（E16.5）和产后第3天（P3）的年龄介于胚胎或年轻的幼崽。 注:骨迷路和颞骨骨化使小鼠成熟清扫越来越复杂。此外kinocilia，唯一真正基于微管纤毛对耳蜗毛细胞中发现，在开发过程中缩回，并且不再存在于成年小鼠。 </li><li>固定后，脱钙成人耳蜗。地点解剖（见第3）骨迷宫，于2ml EDTA（在PBS中4.13％），pH值7.3，在微量离心管3 - 4天的旋转。每天补充EDTA。组织有软化后，冲洗1.5毫升以上PBS 3次，每次5分钟就增加一搅拌章动器。 </li></ol> 3.耳蜗解剖<ol><li>通过颈椎脱位或CO 2吸入安乐死后（100％ 的 CO 2），除去头。用剪子的手术刀刀片或小对，根据动物的大小，沿着矢状中线解剖头在鼻子开始和尾端延伸。一双镊子上卸下从头骨的每一半大脑。识别颞骨，其含有内耳的显影骨迷宫（参见图 1A中的箭头）。 </li><li>使用一对用于牛肝菌仔细分离从头骨（颞骨）骨迷宫。这样做解剖显微镜下。轻轻运行镊子骨迷宫下方PRISE远离颅骨骨组织。在动物实验中达到P4骨迷宫仍然软骨，可以不破坏很容易地删除。 </li><li>剥离之后，使用镊子解剖的尖端清除椭圆形和圆形​​的窗户，让一个小口子耳蜗螺旋的顶点。前蜗管的进一步解剖修复骨迷宫。为了能够容易去除盖膜（见3.7），修复骨迷宫在1.5ml 4％PFA在冰上5分钟。 注意:如果不需要去除盖膜，不再固定是建议（见4.1 - 4.3）。耳蜗管解剖前颞骨的简要固定有助于解剖过程和拆除盖膜。邮政解剖和Corti器的曝光，furt她的固定是必要的。 </li><li>进一步剖析骨迷宫揭露耳蜗感觉上皮如下。将骨迷宫中含有PBS便于清扫一个黑色硅胶elastomere涂层解剖盘。使用minutien销如果需要以固定的组织。使用minutien销，将它们通过骨迷宫朝上耳蜗螺旋的腹侧前庭部。 注意:黑色硅胶elastomere菜:混合硅elastomere基本组件用木炭粉，以获得不透明黑色。添加固化剂并倾入一个或更多个培养皿（玻璃或塑料）。真空干燥去除残留气泡。干菜肴使用之前完全。 </li><li>用细镊子（＃5）删除外软骨暴露蜗管。开始在卵圆窗;插入镊子尖底到卵圆窗，轻轻地撬开软骨，慢慢向上对移动顶尖。 </li><li>耳蜗管曝光后，取出腹面，在赖斯纳的膜。用细对镊子在蜗管的底部夹住Reissner变的膜和在向上运动剥开。形象化的蜗管的背侧，包括感觉上皮。 </li><li>下面（选购）的说明卸下盖膜。对于SEM或kinocilium的免疫组化或纤毛束取出盖膜。 </li><li>使用非常精细的钳子（＃55或更细），在耳蜗的基础掐盖膜，向上剥离走向顶点。 注:盖膜是光学透明的，这使得它难以辨认。往往不是该膜在一块脱落，虽然它不容易显现，因为它是从科尔蒂的暴露器官被拉断人可以感觉到的阻力。 </li><li>暴露柯蒂氏器后，进一步固定组织为d下面旁切。保留前庭区，以帮助组织进一步的准备。 </li></ol> 4.固定<ol><li>对于常规免疫组织化学固定在1.5ml 4％PFA的解剖骨迷宫在4℃下于2小时一章动器。 注意:由于不同的抗体和抗原，变型中的长度和固定的组合物的敏感性，可能需要并应该为每个抗体进行优化。 </li><li>固定后，通过对具有增加的搅动一章动器在1.5ml以上PBS中的3次漂洗5分钟洗涤样品。样品可以处理之前被存储在PBS在4℃几周。 </li><li>如果制备样品的SEM，在SEM中修复弄不好解剖颞骨（参见1.7）中于室温2小时。由1.5毫升以上Hepes缓冲上增加一个搅拌5章动器分3次冲洗清洗。商店在Hepes缓冲液，在4℃直至进一步处理。存储的时间超过几个星期的不推荐秒。 </li></ol> 5.免疫组化<ol><li>对解剖的样品在平底96孔板中的一个孔进行免疫组化分析。或者，使用PCR或离心管中。明智的做法是保留骨迷路的前庭部分，以方便处理。 </li><li>通过在RT上缓慢搅拌一章动器在1.5ml的Triton缓冲孵育1小时透化组织。 </li><li>由0.5毫升三硝基甲苯块孵育在室温下至少1小时的块组织。如果使用鼠标中提出的主要抗体，以1比200稀释（见1.4）添加抗鼠IgG Fab片段，以块。这大大降低了非特异性小鼠组织的抗小鼠IgG的结合。 </li><li>孵育在曲通块O / N轻轻搅拌稀释于4℃初级抗体的组织。抗体稀释取决于所用抗体（参见6.1节）。另外孵化初级antibodieS表示在RT 2小时。理想的情况下使用0.5毫升初级抗体稀释液的最小体积。如果抗体是有限的，使用的抗体稀释度完全包住的组织的最小的体积。 </li><li>通过漂洗1.5毫升以上的Triton缓冲液，15分钟的最小的3倍，在具有增加的搅动一章动器洗净组织。 </li><li>在的Triton块在RT上的章动器1小时孵育在厂家稀释的荧光染料缀合的二级抗体的组织建议的浓度（1000通常为1:200-1）。使用0.5毫升次级抗体稀释液的最小体积。 <ol><li>离心稀释的第二抗体以13,000×g离心以使用3分钟前，以尽量减少二级抗体聚集体的非特异性结合。这一步免受光组织起以避免漂白的荧光染料。 </li></ol></li><li>如在步骤5.5中，由于1.5ml以上的Triton缓冲，最小的3次漂洗洗涤组织15分钟，在一个章动器增加搅拌。在PBS样品储存在4°C，直到准备安装。 </li></ol> 6.抗体选择注:推荐抗体及其稀释液的来源列于具体材料和设备的表中。在第5节进行抗体孵化。 <ol><li>可视化的基于微管kinocilium，使用一​​个纤毛轴丝标记诸如抗Arl13b（1:1000）或抗乙酰-α微管蛋白（1:800）。可视化使用抗体抗γ微管蛋白的基体（1:200），或任何其他中心体标志物。 </li><li>以可视化的肌动蛋白纤维丰富，纤毛束，加毒伞素（1:300 - 1000）偶联到几个不同的荧光团到二级抗体孵育之一。鬼笔环肽还标签其它丝状肌动蛋白的结构包括围绕每个上皮毛细胞的周围的皮质肌动蛋白丝。这是有助于确定各毛细胞的轮廓。使用另一种膜标记物，如抗ZO-1（1:500），如果需要的话。 </li><li>标签使用抗肌球蛋白VI（1:1000）耳蜗毛细胞或肌球蛋白Ⅶa因子（1:1000）。这些名称可能会评估耳蜗长度使用。 </li></ol>注:优化显微镜要求使用合适的荧光染料标记的二抗。 7.安装和影像<ol><li>将含有PBS一个黑色硅胶elastomere菜样本。用细镊子，从耳蜗螺旋删除前庭区。 </li><li>非常小心地取出从耳蜗螺旋底层的软骨和间质。其余耳蜗螺旋包含在内沟，科蒂和外沟的器官。 </li><li>转移耳蜗螺旋入放置在显微镜载玻片上的PBS下降。如果需要的话，在耳蜗螺旋分离成碎片相当于一匝。这个步骤是不必要然而，并可导致步骤l组织的OSS。耳蜗毛细胞的顶端表面（纤毛侧）应朝上朝向盖玻片。 </li><li>吸走的PBS用滤纸的吸附剂组织或片，轻轻地重新定位耳蜗螺旋如果上皮细胞已经转移和重叠到自身。 </li><li>添加安装媒体的直接下降到耳蜗样品，轻轻地在上面放置盖玻片，照顾，以避免气泡。无间隔是必需的;直接放置在盖玻片样品上。一种水溶性的，非荧光的，半永久性的安装平台，它不需要额外的步骤来保持在适当位置的盖玻片建议。安装媒体和盖玻片厚度应匹配显微镜规格。 </li><li>使用配备有高倍率（63 - 100X）啶或激光扫描共聚焦显微镜，高数值孔径（1.2 - 1.4）的目标捕捉耳蜗毛细胞的顶端表面的图像。使用LOWER目标（5 - 20X）取重叠耳蜗螺旋的图像，以量化所述蜗管的长度。匹配激发激光器和发射滤波器来用于第二抗体的荧光基团。 </li></ol> 8.扫描电子显微镜<ol><li>从第4.3节继续。在Hepes缓冲液洗涤SEM固定的样品后，执行下通风以下步骤。以下方案可以很好地用于耳蜗组织并避免了与导电金属的使用溅射镀膜的。 </li><li>后修复程序中的1％OSO 4在Hepes缓冲液1小时，随后洗涤3次用1毫升，每次5分钟，蒸馏水。 OSO 4的最小体积完全包住的组织应该被用来减少有毒废物。没有搅拌是必需的。 </li><li>孵育在RT样品中的每个下面的解决方案，为1小时，以3次洗涤用1毫升蒸馏水，每次5分钟，在步骤之间:1％鞣酸水和FIL新鲜的使用前羊羔; 1％OSO 4在水中，在水中1％单宁酸，1％OSO 4中的水。 </li><li> 30，50，70，90，和95％的:通过温育梯度乙醇系列中的每个下面的稀释液10分钟，脱水样品。没有搅拌是必需的。 </li><li>通过三个变化，每次5分钟，100％乙醇的转移样品（从200标准乙醇的新开瓶）。 </li><li>运行虽然临界点干燥器下列制造商的说明将样品。 </li><li>安装上使用于成像在一个电子显微镜之前的SEM存根的顶部导电性碳粘合剂样品。在立体显微镜，用一双细镊子和画笔轻轻样品与耳蜗上皮朝上的位置。使用示例的前庭部为"锚"的组织的残余部分。样品储存在干燥器中，直到成像。在琼斯（2012）21中描述进行SEM成像。 </li></ol> 9。量化<ol><li>免疫组化准备后，获取使用啶或激光扫描共聚焦显微镜图像。用于SEM制备后，使用扫描型电子显微镜图像的标本。图像尔蒂与暴露的耳蜗毛细胞和闰支持细胞的器官的顶端表面。 </li><li>定义特定位置沿耳蜗管，如25，50，以及从基部75％，并利用这些突变体和对照样品之间耳蜗区域进行比较。分析并与他们同窝对照比较纤毛的突变体，如遗传背景的差异可以修改耳蜗的表型。 注:Corti器的开发中，从朝向顶点和基部两者中间基座延伸的梯度。在小鼠，发育不完全，直到P14，所以在相似的发展阶段和立场进行比较的区域是非常重要的。 </li><li>使用附带的软件的异体显微镜拍照w表示该特定表型的量化的要求（见下文）。使用图像分析软件，如图像J或软件附带的显微镜测量长度，细胞计数和确定，如下所述蛋白定位。这些图形数据为条形图，散点图，箱印迹或直方图，比较突变体与控制。 </li><li>耳蜗管（图3A）的总长度: <ol><li>使用毛细胞标志物或鬼笔环肽，（这标志着纤毛束），确定并测量其中感觉上皮开始和结束。耳蜗管的长度通常短于纤毛突变体。 </li></ol></li><li>纤毛束异常（ 图3B，D，E，G）: <ol><li>测量束凸（高度）作为该包的顶点，并且通过如在图3G中所示的束"臂"的两端延伸的线之间的最短距离，离开。另外，量化区如图3G，向右外毛细胞纤毛束的武器包围。如果毛细胞具有圆形纤毛束可以被识别计为总毛细胞的百分比。 注:在许多纤毛束的突变体的异常可以观察到，不论束方向。它难以准确地量化纤毛束异常。 </li></ol></li><li>在纤毛束（图3B，C，G）的 ​​方向: <ol><li>评估各个相对束的方向，以垂直延伸，以分隔所述内和外毛细胞支柱细胞的行的线。与正常的取向单元沿此垂直轴对准，因此有0°的旋转。使用一个360°的符号或绝对偏离0°判断旋转角度。 </li></ol></li><li> Kinocilia定位或纤毛束定位（ 图3B，F，H）: <ol><li>伯爵在kinocilia缺少细胞的百分比。测量到该包的"顶点"或中心，距离kinocilium的距离。的束的"顶点"可能不容易确定，如果包是异常，所以束的中心，可以替代使用。 </li></ol></li><li>量化kinocilia和纤毛束的位置根尖毛细胞表面上，通过覆盖的位置的网格上的每个毛细胞和标记kinocilium任碱或纤毛束的顶点/中心的位置。将数据显示为每个类别的百分比位于网格的一个特定区域内，并通过叠置每个标记的位置到一个位置的网格。 注:在控制组织，kinocilia总是附着在纤毛束的顶点。在纤毛突变体，kinocilia经常丢失，错误定位但仍附着，或甚至完全从S脱离tereociliary捆绑。 </li><li> Kinocilia长度（图3I）: <ol><li>通过用纤毛轴丝标记标记测量kinocilium的长度。唯一的衡量标准，一个1.5微米的激光共聚焦平面内躺平kinocilia。确认纤毛通过观察扫描的组织的剖视图平躺。从耳蜗的相同区域相比较老化匹配样本由于kinocilium开发期间缩回。 </li></ol></li><li>极性蛋白的错误定位: <ol><li>以下使用抗极性蛋白质，如Vangl2和Gαi3免疫组化，确定通过影像定位。 </li></ol></li></ol>注:在某些纤毛突变，极性蛋白的本地化被打乱。这些包括Vangl2和Gαi3，这已被证明在Ift20，Bbs8和BBS6突变耳蜗被打乱。 注:如何量化和显示毛细胞POLARIT进一步的例子y可能在下面的文章中找到。 Curtin的，等。 （2003）当代生物学22，Montcouquiol，等。 （2003）自然7，王等人（2006）神经科学杂志23，Montcouquiol，等。 （2008）分子生物学24，5月Simera等方法。 （2012）分子生物学方法25，尹等人（2012）公共科学图书馆·26之一。

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The author declares no competing financial interests.

当准备耳蜗组织进行分析，有要记住几个关键点。首先，在遗传背景的差异可以修改耳蜗的表型，因此有必要进行分析和比较只同窝对照。其次，需要彻底清除盖膜获得具有免疫最好的图像，是SEM至关重要。盖膜是不透明结构，并且可以直接模糊感觉上皮的细胞其下方，使得成像更具挑战性。偶尔在加工过程中，盖膜可能会退缩，露出毛细胞。即使在这些情况下，除去强烈建议。这一步需要耐心?...

初级纤毛是长基于微管附属物，从大多数哺乳动物细胞的表面上延伸。初级纤毛经常被混淆与运动纤毛，其中总有每个细胞多，而其目的是在整个膜表面移动的液体。初级纤毛，与此相反，采用感觉角色并因此也被称为感觉纤毛。一旦早已被人遗忘，这种细胞器最近被"重新发现"它与人类遗传病1的众多协会的结果。理想的位置作为信号的细胞器，初级纤毛已显示调节众多信号通路，其中有许多是不仅在组织稳态和疾病重要的，但也发展2中。 示出一个将与纤毛功能障碍相关联的第一信号通路是非典型Wnt信号传导途径，也被称为平面细胞极性（PCP）途径<sup<html> &gt; 3。在果蝇中初步确定这信号级联反应，是胚胎发育的关键;特别是用于会聚和扩展过程和细胞在上皮4的平面中的正确方向。设置调节蛋白的核心的顺序信令转换方向提示这最终导致细胞骨架重排，并导致上皮细胞在平面5的协调极化。衔接和延伸的过程是绝对必需的蜗管伸长和正确的蜂窝图案6。由于这是通过PCP途径的激活调节，耳蜗PCP突变体的最显着的表型中的一个是一个缩短的蜗管与紊乱感觉上皮7。同样，小鼠突变，缺乏纤毛，也表现出这样的融合和扩展型8,9，但恰恰这是如何调控仍有待澄清。 ve_content"&gt;由于收敛和扩展步骤是耳蜗管的生长，以及蜗管内的感觉上皮细胞图案化临界，显影耳蜗是其中脊椎动物发育过程中检查PCP信令理想器官。的器官尔蒂，给予该线耳蜗管，是由必须被均匀地取向为耳蜗的功能10非感官支持细胞和mechanosensory毛细胞的专门感觉上皮的术语。本mechanosensory毛细胞是所谓的由于从表皮板延伸纤毛束每个感觉毛细胞11（顶面）。这些充当机械感觉的，尽管其命名为纤毛主要传感器，实际上是由改性肌动蛋白基于灯丝的微绒毛。在每个字形的头发束，三排纤毛的以高度有序的和常规巴被组织ttern在楼梯状的方式。真实基于微管纤毛，称为kinocilia，需要用于该纤毛束 12的发展和方向。在每次毛细胞，一个单一的kinocilium被物理连接到纤毛束，位于中央相邻纤毛的最高行。该kinocilium的确切功能尚不清楚，一个假设是，因为他们从微绒毛12成熟kinocilium&#39;拉&#39;的纤毛成形。在脊椎动物中，在耳蜗kinocilia仅存在瞬时和从头发细胞之前听到11,13,14的发作缩回小鼠。 在严重缩短耳蜗管显影耳蜗结果纤毛的完全丧失，错形成及误取向纤毛束，以及错误置位的基体8,9。一个功能纤毛不只是由纤毛轴丝的。纤毛相关的许多蛋白质功能发生在本地化的纤毛相关的子域复合物，如基体，过渡区，或纤毛轴丝15。基础体温，从中心体的中心粒母亲衍生，也是从纤毛向外延伸进入细胞体内微管微管组织中心并能调节细胞内贩卖和走私纤毛。睫状肌的过渡区是纤毛功能被组织纤毛化合物16的进口和出口方面管制的另一个区域。 多个研究已经确定纤毛和非经典Wnt（PCP信令）之间的连接，虽然确切机制尚不清楚17。睫状和PCP基因冗余和细胞极性的广义细胞异常的敏感性，使得难以突变直接链接到特定的PCP-赤字。一个PCP信令的读出出局的是基体和PRIMAR的定位Ÿ纤毛，因此分离主要由二次缺陷是具有挑战性的。在斑马鱼和小鼠突变一些研究表明信号18-20纤毛和Wnt之间没有联系。在数据差异可能反映物种，组织，或在朝向Wnt信号睫状捐款颞依赖性差异。此外，如果基体保持工作正常Wnt信号的响应可能会被保留。一个更深入的了解纤毛蛋白在细胞信号通路及其它生物现象的作用，是对我们的细胞和发育生物学的理解，以及为有针对性的治疗策略的发展至关重要。

<table><tbody><tr><td>Tools/Equipment</td><td></td><td></td><td></td></tr><tr><td>Silicone elastomere - Sylgard 184</td><td>Sigma-Aldrich</td><td>761028-5EA</td><td>See Note 2</td></tr><tr><td>Micro dissecting scissors-straight blade</td><td>Various</td><td></td><td></td></tr><tr><td>Fine forceps (no. 5 and 55) and blunt forceps</td><td>Various</td><td></td><td></td></tr><tr><td>Dissecting microscope.</td><td>Various</td><td></td><td></td></tr><tr><td>Uncoated glass microscope slides</td><td>Various</td><td></td><td></td></tr><tr><td>Microscope cover slips (22 mm &amp;times; 40 mm &amp;times; 0.15 mm)</td><td>Various</td><td></td><td></td></tr><tr><td>Transfer pipettes</td><td>Various</td><td></td><td></td></tr><tr><td>Minutien pins</td><td>&amp;nbsp;Fine Science Tools</td><td>26002-10</td><td></td></tr><tr><td>SEM sample holder</td><td>tousimis</td><td>8762</td><td></td></tr><tr><td>Scanning electron microscopy studs</td><td>TED PELLA</td><td>16111</td><td></td></tr><tr><td>PELCO Tabs: Carbon adhesive</td><td>TED PELLA</td><td>16084-3</td><td></td></tr><tr><td>Fluorescent Microscope</td><td>Various</td><td></td><td></td></tr><tr><td>Critical Point Dryer</td><td>Various</td><td></td><td></td></tr><tr><td>Scanning Electron Microscope</td><td>Various</td><td></td><td></td></tr><tr><td>Glass microscope slides</td><td>Various</td><td></td><td></td></tr><tr><td>Glass coverslips</td><td>Various</td><td></td><td></td></tr><tr><td>Kimwipe Tissue&amp;nbsp;</td><td>Various</td><td></td><td></td></tr><tr><td>Fine Paint Brush</td><td></td><td></td><td></td></tr><tr><td>Reagents</td><td></td><td></td><td></td></tr><tr><td>1&amp;times; Phosphate buffered saline (PBS)</td><td>Gibco/Life Technologies</td><td>10010023</td><td></td></tr><tr><td>Paraformaldehyde&amp;nbsp; (PFA) (EM Grade Required for EM)</td><td>Various</td><td></td><td>Prepare a 4% solution in 1&amp;times; PBS made fresh each time. EM Grade Required for EM.</td></tr><tr><td>2.5% Glutaraldehyde Grade1</td><td>Sigma-Aldrich</td><td>G5882</td><td></td></tr><tr><td>Tris-HCl (pH 7.5)</td><td>Various</td><td></td><td></td></tr><tr><td>NaCl</td><td>Various</td><td></td><td></td></tr><tr><td>CaCl 2</td><td>Various</td><td></td><td></td></tr><tr><td>Triton X-100</td><td>Various</td><td></td><td></td></tr><tr><td>Normal Goat Serum</td><td>Various</td><td></td><td></td></tr><tr><td>AffiniPure Fab Fragment Donkey Anti-Mouse IgG (H+L)</td><td>Jackson ImmunoResearch</td><td>715-007-003</td><td></td></tr><tr><td>Fluoromount-G Mounting media</td><td>SouthernBiotech</td><td>0100-01</td><td></td></tr><tr><td>10&amp;times; Hanks&amp;rsquo; Balanced Salt Solution (HBSS)</td><td>Gibco/Life Technologies</td><td>14065</td><td></td></tr><tr><td>Hepes</td><td>Gibco/Life Technologies</td><td>15630-080</td><td></td></tr><tr><td>Osmium tetroxide (OsO4 )</td><td>Sigma-Aldrich/Fluka Analytical</td><td>75632</td><td></td></tr><tr><td>Tannic acid</td><td>Sigma-Aldrich</td><td>403040</td><td></td></tr><tr><td>Ethanol 200 proof</td><td>Various</td><td></td><td></td></tr><tr><td>Antibodies</td><td></td><td></td><td></td></tr><tr><td>anti Arl13b</td><td>Protein Tech</td><td>17711-1-AP</td><td>Suggested concentration 1:1,000</td></tr><tr><td>anti acetylated tubulin (611-B1)</td><td>Sigma-Aldrich</td><td>T6793</td><td>Suggested concentration 1:800</td></tr><tr><td>anti gamma tubulin (GTU-88)</td><td>Sigma-Aldrich</td><td>T6557</td><td>Suggested concentration 1:200</td></tr><tr><td>anti Zo_1&amp;nbsp;</td><td>Invitrogen</td><td>40-2300</td><td>Suggested concentration 1:500</td></tr><tr><td>Myosin VI</td><td>Proteus Biosciences</td><td>25-6791</td><td>Suggested concentration 1:1000</td></tr><tr><td>Myosin VIIa</td><td>Proteus Biosciences</td><td>25-6790</td><td>Suggested concentration 1:1,000</td></tr><tr><td>anti Vangl2</td><td>Merk Millipore</td><td>ABN373</td><td>Suggested concentration 1:250</td></tr><tr><td>anti G&amp;alpha;i3</td><td>Sigma-Aldrich</td><td>G4040</td><td>Suggested concentration 1:250</td></tr><tr><td>Alexa Fluor&amp;reg; 488 Phalloidin</td><td>Invitrogen/Life Technologies</td><td>A12379</td><td>Suggested concentration 1:300 - 1,000</td></tr><tr><td>Alexa Fluor&amp;reg; 568 Phalloidin</td><td>Invitrogen/Life Technologies</td><td>A12380</td><td>Suggested concentration 1:300 - 1,000</td></tr></tbody></table>

evaluation of planar-cell-polarity phenotypes in ciliopathy mouse mutant cochlea

In recent years, primary cilia have emerged as key regulators in development and disease by influencing numerous signaling pathways. One of the earliest signaling pathways shown to be associated with ciliary function was the non-canonical Wnt signaling pathway, also referred to as planar cell polarity (PCP) signaling. One of the best places in which to study the effects of planar cell polarity (PCP) signaling during vertebrate development is the mammalian cochlea. PCP signaling disruption in the mouse cochlea disrupts cochlear outgrowth, cellular patterning and hair cell orientation, all of which are affected by cilia dysfunction. The goal of this protocol is to describe the analysis of PCP signaling in the developing mammalian cochlea via phenotypic analysis, immunohistochemistry and scanning electron microscopy. Defects in convergence and extension are manifested as a shortening of the cochlear duct and/or changes in cellular patterning, which can be quantified following dissection from developing mouse mutants. Changes in stereociliary bundle orientation and kinocilia length or positioning can be observed and quantitated using either immunofluorescence or scanning electron microscopy (SEM). A deeper insight into the role of ciliary proteins in cellular signaling pathways and other biological phenomena is crucial for our understanding of cellular and developmental biology, as well as for the development of targeted treatment strategies.

耳蜗解剖和组织准备 去除大脑后，P0老鼠头，骨迷路，从后面看，可以看到（ 图1A，白色箭头），并取消后中线矢状解剖图1B显示了耳蜗毛孤立骨迷宫朝上，腹，（左）和从后面，背（右）。白色箭头指向卵圆窗从中可以开始除去外软骨。一旦外软骨已经完全除去，暴露的耳蜗管，仍完好...

Watch this Scientific Journal Video about Evaluation of Planar-Cell-Polarity Phenotypes in Ciliopathy Mouse Mutant Cochlea at JoVE.com

Evaluation of Planar-Cell-Polarity Phenotypes in Ciliopathy Mouse Mutant Cochlea

在Ciliopathy鼠标突变耳蜗平面 - 细胞极性表型的评价

Primary cilia influence various signaling pathways. The mammalian cochlea is ideal for examining planar cell polarity (PCP) signaling. Cilia dysfunction affects cochlear outgrowth, cellular patterning and hair cell orientation, readouts of PCP. Our goal is to analyze PCP signaling in mouse cochlea via phenotypic analysis, immunohistochemistry and scanning electron microscopy.

In recent years, primary cilia have emerged as key regulators in development and disease by influencing numerous signaling pathways. One of the earliest ...

evaluation-planar-cell-polarity-phenotypes-ciliopathy-mouse-mutant

Universidad de Cartagena UDEC

Research

JoVE Journal

Medicine

10.3K 次观看.  Johannes Gutenberg-Universität Mainz. Primary cilia influence various signaling pathways. The mammalian cochlea is ideal for examining planar cell polarity (PCP) signaling. Cilia dysfunction affects cochlear outgrowth, cellular patterning and hair cell orientation, readouts of PCP. Our goal is to analyze PCP signaling in mouse cochlea via phenotypic analysis, immunohistochemistry and scanning electron microscopy.

视频: Evaluation of Planar-Cell-Polarity Phenotypes in Ciliopathy Mouse Mutant Cochlea

Culture of Embryonic Mouse Cochlear Explants and Gene Transfer by Electroporation

Auditory hair cells located within the mouse organ of Corti detect and transmit sound information to the central nervous system. The mechanosensory hair cells are aligned in one row of inner hair cells and three rows of outer hair cells that extend along the basal to apical axis of the cochlea. The explant culture technique described here provides an efficient method to isolate and maintain cochlear explants from the embryonic mouse inner ear. Also, the morphology and molecular characteristics of sensory hair cells and nonsensory supporting cells within the cochlear explant cultures resemble those observed in vivo and can be studied within its intrinsic cellular environment. The cochlear explants can serve as important experimental tools for the identification and characterization of molecular and genetic pathways that are involved in cellular specification and patterning. Although transgenic mouse models provide an effective approach for gene expression studies, a considerable number of mouse mutants die during embryonic development thereby hindering the analysis and interpretation of developmental phenotypes. The organ of Corti from mutant mice that die before birth can be cultured so that their in vitro development and responses to different factors can be analyzed. Additionally, we describe a technique for electroporating embryonic cochlear explants ex vivo which can be used to downregulate or overexpress specific gene(s) and analyze their potential endogenous function and test whether specific gene product is necessary or sufficient in a given context to influence mammalian cochlear development1-8.

We present a method that describes isolation and culture of cochlear explants from embryonic mouse inner ear. We also demonstrate a method for gene transfer into cochlear explants via square-wave electroporation. The in vitro explant culture coupled with gene transfer technique enables researchers to study the effects of altering gene expression during development.

小鼠胚胎植耳蜗的文化和基因转移通过电穿孔

Auditory hair cells located within the mouse organ of Corti detect and transmit sound information to the central nervous system. The mechanosensory hair ...

科研

发育生物学

Isolating LacZ-expressing Cells from Mouse Inner Ear Tissues using Flow Cytometry

Isolation of specific cell types allows one to analyze rare cell populations such as stem/progenitor cells. Such an approach to studying inner ear tissues presents a unique challenge because of the paucity of cells of interest and few transgenic reporter mouse models. Here, we describe a protocol using fluorescence-conjugated probes to selectively label LacZ-positive cells from the neonatal cochleae.
The most common underlying pathology of sensorineural hearing loss is the irreversible damage and loss of cochlear sensory hair cells, which are required to transduce sound waves to neural impulses. Recent evidence suggests that the murine auditory and vestibular organs harbor stem/progenitor cells that may have regenerative potential1,2. These findings warrant further investigation, including identifying specific cell types with stem/progenitor cell characteristics. The Wnt signaling pathway has been demonstrated to play a critical role in maintaining stem/progenitor cell populations in several organ systems3-7. We have recently identified Wnt-responsive Axin2-expressing cells in the neonatal cochlea, but their function is largely unknown8.
To better understand the behavior of these Wnt-responsive cells in vitro, we have developed a method of isolating Axin2-expressing cells from cochleae of Axin2-LacZ reporter mice9. Using flow cytometry to isolate Axin2-LacZ positive cells from the neonatal cochleae, we could in turn execute a variety of experiments on live cells to interrogate their behavior as stem/progenitor cells. Here, we describe in detail the steps for the microdissection of neonatal cochlea, dissociation of these tissues, labeling of the LacZ-positive cells using a fluorogenic substrate, and cell sorting. Techniques for dissociating cochleae into single cells and isolating cochlear cells via flow cytometry have been described2,10-12. We have made modifications to these techniques to establish a novel protocol to isolate LacZ-expressing cells from the neonatal cochlea.

Flow cytometry is a powerful tool allowing for the isolation and study of specific cell populations. This protocol describes steps for isolating LacZ-expressing cells from cochlear tissues from neonatal transgenic mice. Dissociated cochlear cells were labeled using fluorescent-conjugated substrates of &#946;-galactosidase prior to separation via flow cytometry.

隔离LacZ基因表达的小鼠内耳组织用流式细胞仪检测细胞

Isolation of specific cell types allows one to analyze rare cell populations such as stem/progenitor cells. Such an approach to studying inner ear tissues ...

神经科学

Long-term Time Lapse Imaging of Mouse Cochlear Explants

Here we present a method for long-term time-lapse imaging of live embryonic mouse cochlear explants. The developmental program responsible for building the highly ordered, complex structure of the mammalian cochlea proceeds for around ten days. In order to study changes in gene expression over this period and their response to pharmaceutical or genetic manipulation, long-term imaging is necessary. Previously, live imaging has typically been limited by the viability of explanted tissue in a humidified chamber atop a standard microscope. Difficulty in maintaining optimal conditions for culture growth with regard to humidity and temperature has placed limits on the length of imaging experiments. A microscope integrated into a modified tissue culture incubator provides an excellent environment for long term-live imaging. In this method we demonstrate how to establish embryonic mouse cochlear explants and how to use an incubator microscope to conduct time lapse imaging using both bright field and fluorescent microscopy to examine the behavior of a typical embryonic day (E) 13 cochlear explant and Sox2, a marker of the prosensory cells of the cochlea, over 5 days.

Live imaging of the embryonic mammalian cochlea is challenging because the developmental processes at hand operate on a temporal gradient over ten days. Here we present a method for culturing and then imaging embryonic cochlear explant tissue taken from a fluorescent reporter mouse over five days.

老鼠耳蜗外植体的长期时间推移成像

Here we present a method for long-term time-lapse imaging of live embryonic mouse cochlear explants. The developmental program responsible for building ...

Whole Mount Dissection and Immunofluorescence of the Adult Mouse Cochlea

The organ of Corti, housed in the cochlea of the inner ear, contains mechanosensory hair cells and surrounding supporting cells which are organized in a spiral shape and have a tonotopic gradient for sound detection. The mouse cochlea is approximately 6 mm long and often divided into three turns (apex, middle, and base) for analysis. To investigate cell loss, cell division, or mosaic gene expression, the whole mount or surface preparation of the cochlea is useful. This dissection method allows visualization of all cells within the organ of Corti when combined with immunostaining and confocal microscopy to image cells at different planes in the z-axis. Multiple optical cross-sections can also be obtained from these z-stack images. In addition, the whole mount dissection method can be used for scanning electron microscopy, although a different fixation method is needed. Here, we present a method to isolate the organ of Corti as three intact cochlear turns (apex, middle, and base). This method can be used for mice ranging from one week of age through adulthood and differs from the technique used for neonatal samples where calcification of the cochlea is incomplete. A slightly modified version can be used for dissection of the rat cochlea. We also demonstrate a procedure for immunostaining with fluorescently tagged antibodies.

We present a method to isolate the adult organ of Corti as three intact cochlear turns (apex, middle, and base). We also demonstrate a procedure for immunostaining with fluorescently tagged antibodies. Together these techniques allow the study of hair cells, supporting cells, and other cell types found in the cochlea.

全山解剖和成年小鼠耳蜗的免疫

The organ of Corti, housed in the cochlea of the inner ear, contains mechanosensory hair cells and surrounding supporting cells which are organized in a ...

Cryosectioning and Immunostaining Mouse Inner Ear Tissue: From Embryonic to Adult Stages

This protocol details general histology methods for preparing inner ear samples from embryonic, neonatal, and adult mice. The purpose of this protocol is to provide a straightforward and standardized method for inner ear tissue processing for researchers, possibly new to the field, interested in working with the mouse cochlea. Included here are protocols for dissection, fixation, embedding, cryosectioning, and immunostaining. Section immunostaining is one of the best methods for examining individual cells within the context of the entire cochlea.
Key steps include dissecting the inner ear away from the skull, fixing the tissue using 4% paraformaldehyde, embedding with Optimal Cutting Temperature compound, cryosectioning, and immunostaining with antibodies targeting specific proteins expressed by the cochlea.
Included in our methods are special considerations made for the cochlea given its 
shape and structure.&#160;Reasonably good focus and dissection skills are needed, as tissue damage can affect the quality of immunostaining and consistency among samples. However, with the procedures we outline, most users can be trained in a few weeks to make beautiful preparations. Overall, this protocol offers a valuable way to promote research to understand auditory development, function, and disease in mouse models.

This protocol, intended for novice users of mouse inner ear tissue, comprehensively details steps for processing mouse inner ears at different developmental stages for section immunostaining.

小鼠内耳组织的冷冻切片和免疫染色：从胚胎阶段到成人阶段

This protocol details general histology methods for preparing inner ear samples from embryonic, neonatal, and adult mice. The purpose of this protocol is ...

Morphological and Functional Evaluation of Ribbon Synapses at Specific Frequency Regions of the Mouse Cochlea

Cochlear inner hair cells (IHCs) transmit acoustic signals to spiral ganglion neurons (SGNs) through ribbon synapses. Several experimental studies have indicated that hair cell synapses may be the initial targets in sensorineural hearing loss (SNHL). Such studies have proposed the concept of cochlear &#34;synaptopathy&#34;, which refers to alterations in ribbon synapse number, structure, or function that result in abnormal synaptic transmission between IHCs and SGNs. While cochlear synaptopathy is irreversible, it does not affect the hearing threshold. In noise-induced experimental models, restricted damage to IHC synapses in select frequency regions is employed to identify the environmental factors that specifically cause synaptopathy, as well as the physiological consequences of disturbing this inner ear circuit. Here, we present a protocol for analyzing cochlear synaptic morphology and function at a specific frequency region in adult mice. In this protocol, cochlear localization of specific frequency regions is performed using place-frequency maps in conjunction with cochleogram data, following which the morphological characteristics of ribbon synapses are evaluated via synaptic immunostaining. The functional status of ribbon synapses is then determined based on the amplitudes of auditory brainstem response (ABR) wave I. The present report demonstrates that this approach can be used to deepen our understanding of the pathogenesis and mechanisms of synaptic dysfunction in the cochlea, which may aid in the development of novel therapeutic interventions.

This manuscript describes an experimental protocol for evaluating the morphological characteristics and functional status of ribbon synapses in normal mice. The present model is also suitable for noise-induced and age-related cochlear synaptopathy-restricted models. The correlative results of previous mouse studies are also discussed.

小鼠耳蜗特定频率区域带状带突起的形态和功能评估

Cochlear inner hair cells (IHCs) transmit acoustic signals to spiral ganglion neurons (SGNs) through ribbon synapses. Several experimental studies have ...

Cochlear Surface Preparation in the Adult Mouse

Auditory processing in the cochlea depends on the integrity of the mechanosensory hair cells. Over a lifetime, hearing loss can be acquired from numerous etiologies such as exposure to excessive noise, the use of ototoxic medications, bacterial or viral ear infections, head injuries, and the aging process. Loss of sensory hair cells is a common pathological feature of the varieties of acquired hearing loss. Additionally, the inner hair cell synapse can be damaged by mild insults. Therefore, surface preparations of cochlear epithelia, in combination with immunolabeling techniques and confocal imagery, are a very useful tool for the investigation of cochlear pathologies, including losses of ribbon synapses and sensory hair cells, changes in protein levels in hair cells and supporting cells, hair cell regeneration, and determination of report gene expression (i.e., GFP) for verification of successful transduction and identification of transduced cell types. The cochlea, a bony spiral-shaped structure in the inner ear, holds the auditory sensory end organ, the organ of Corti (OC). Sensory hair cells and surrounding supporting cells in the OC are contained in the cochlear duct and rest on the basilar membrane, organized in a tonotopic fashion with high-frequency detection occurring in the base and low-frequency in the apex. With the availability of molecular and genetic information and the ability to manipulate genes by knockout and knock-in techniques, mice have been widely used in biological research, including in hearing science. However, the adult mouse cochlea is miniscule, and the cochlear epithelium is encapsulated in a bony labyrinth, making microdissection difficult. Although dissection techniques have been developed and used in many laboratories, this modified microdissection method using cell and tissue adhesive is easier and more convenient. It can be used in all types of adult mouse cochleae following decalcification.

This article presents a modified cochlear surface preparation method that requires decalcification and use of a cell and tissue adhesive to adhere the pieces of cochlear epithelia to 10 mm round cover slips for immunohistochemistry in adult mouse cochleae.

成年小鼠中的科利耳表面制备

Auditory processing in the cochlea depends on the integrity of the mechanosensory hair cells. Over a lifetime, hearing loss can be acquired from numerous ...

Whole Neonatal Cochlear Explants as an In vitro Model

Untreated hearing loss imposes significant costs on the global healthcare system and impairs individuals' quality of life. Sensorineural hearing loss is characterized by the cumulative and irreversible loss of sensory hair cells and auditory nerves in the cochlea. Entire and vital cochlear explants are one of the fundamental tools in hearing research to detect hair cell loss and to characterize the molecular mechanisms of the inner ear cells. Many years ago, a protocol for neonatal cochlear isolation was developed, and although it has been modified over time, it still holds potential for improvement. 
This paper presents an optimized protocol for isolating and culturing whole neonatal cochlear explants in multi-well culture chambers that enables the study of hair cells and spiral ganglion neuron cells along the entire length of the cochlea. The protocol was tested using cochlear explants from mice and rats. Healthy cochlear explants were obtained to study the interaction between hair cells, spiral ganglion neuron cells, and the surrounding supporting cells. 
One of the main advantages of this method is that it simplifies the organ culture steps without compromising the quality of the explants. All three turns of the organ of Corti are attached to the bottom of the chamber, which facilitates in vitro experiments and the comprehensive analysis of the explants. We provide some examples of cochlear images from different experiments with live and fixed explants, demonstrating that the explants retain their structure despite exposure to ototoxic drugs. This optimized protocol can be widely used for the integrative analysis of the mammalian cochlea.

Whole Neonatal Cochlear Explants as an In vitro Model

The current protocol updates previous protocols and incorporates relatively straightforward approaches for culturing high-quality cochlear explants. This provides reliable data acquisition and high-resolution imaging in live and fixed cells. This protocol supports the ongoing trend of studying inner ear cells.

整个新生儿耳蜗外植体作为 体外 模型

Untreated hearing loss imposes significant costs on the global healthcare system and impairs individuals' quality of life. Sensorineural hearing loss is ...

Dissection of the Auditory Bulla in Postnatal Mice: Isolation of the Middle Ear Bones and Histological Analysis

In most mammals, auditory ossicles in the middle ear, including the malleus, incus and stapes, are the smallest bones. In mice, a bony structure called the auditory bulla houses the ossicles, whereas the auditory capsule encloses the inner ear, namely the cochlea and semicircular canals. Murine ossicles are essential for hearing and thus of great interest to researchers in the field of otolaryngology, but their metabolism, development, and evolution are highly relevant to other fields. Altered bone metabolism can affect hearing function in adult mice, and various gene-deficient mice show changes in morphogenesis of auditory ossicles in utero. Although murine auditory ossicles are tiny, their manipulation is feasible if one understands their anatomical orientation and 3D structure. Here, we describe how to dissect the auditory bulla and capsule of postnatal mice and then isolate individual ossicles by removing part of the bulla. We also discuss how to embed the bulla and capsule in different orientations to generate paraffin or frozen sections suitable for preparation of longitudinal, horizontal, or frontal sections of the malleus. Finally, we enumerate anatomical differences between mouse and human auditory ossicles. These methods would be useful in analyzing pathological, developmental and evolutionary aspects of auditory ossicles and the middle ear in mice.

We present a protocol to isolate the auditory bulla, capsule, and ossicles from postnatal mice for whole mount and histological analysis.

在出生后的小鼠听泡解剖:中耳骨骼和组织学分析的分离

In most mammals, auditory ossicles in the middle ear, including the malleus, incus and stapes, are the smallest bones. In mice, a bony structure called ...

生物学

Dissection of the Endolymphatic Sac from Mice

The study of mutant mouse models of human hearing and balance disorders has unraveled many structural and functional changes which may contribute to the human phenotypes. Although important progress has been done in the understanding of the development and function of the neurosensory epithelia of the cochlea and vestibula, limited knowledge is available regarding the development, cellular composition, molecular pathways and functional characteristics of the endolymphatic sac. This is, in large part, due to the difficulty of visualizing and microdissecting this tissue, which is an epithelium comprised of only one cell layer. The study presented here describes an approach to access and microdissect the endolymphatic sac from the wild-type mouse inner ear at different ages. The result of a similar dissection is shown in a pendrin-deficient mouse model of enlargement of the vestibular aqueduct. A transgenic mouse with a fluorescent endolymphatic sac is presented. This reporter mouse can be used to readily visualize the endolymphatic sac with limited dissection and determine its size. It can also be used as an educational tool to teach how to dissect the endolymphatic sac. These dissection procedures should facilitate further characterization of this understudied part of the inner ear.

<meta charset="utf8"></head><body>小鼠内淋巴囊解剖

This study describes how to dissect the endolymphatic sac from the inner ear of the mouse at different ages. The result of a similar dissection is shown in an Slc26a4-null mouse model of enlargement of the endolymphatic sac. A transgenic mouse with a fluorescent reporter expressed in the endolymphatic sac is presented as a model to readily visualize the endolymphatic sac, and educational tool.

小鼠内淋巴囊解剖

The study of mutant mouse models of human hearing and balance disorders has unraveled many structural and functional changes which may contribute to the ...

在Ciliopathy鼠标突变耳蜗平面 - 细胞极性表型的评价

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此视频中的章节

小鼠胚胎植耳蜗的文化和基因转移通过电穿孔

隔离LacZ基因表达的小鼠内耳组织用流式细胞仪检测细胞

老鼠耳蜗外植体的长期时间推移成像

全山解剖和成年小鼠耳蜗的免疫

小鼠内耳组织的冷冻切片和免疫染色：从胚胎阶段到成人阶段

小鼠耳蜗特定频率区域带状带突起的形态和功能评估

成年小鼠中的科利耳表面制备

整个新生儿耳蜗外植体作为体外模型

在出生后的小鼠听泡解剖:中耳骨骼和组织学分析的分离

小鼠内淋巴囊解剖

在Ciliopathy鼠标突变耳蜗平面 - 细胞极性表型的评价

摘要

探索更多视频

此视频中的章节

小鼠胚胎植耳蜗的文化和基因转移通过电穿孔

隔离LacZ基因表达的小鼠内耳组织用流式细胞仪检测细胞

老鼠耳蜗外植体的长期时间推移成像

全山解剖和成年小鼠耳蜗的免疫

小鼠内耳组织的冷冻切片和免疫染色：从胚胎阶段到成人阶段

小鼠耳蜗特定频率区域带状带突起的形态和功能评估

成年小鼠中的科利耳表面制备

整个新生儿耳蜗外植体作为 体外 模型

在出生后的小鼠听泡解剖:中耳骨骼和组织学分析的分离

小鼠内淋巴囊解剖

整个新生儿耳蜗外植体作为体外模型