Venkatesan Nandakumar, Boggs Kristin, Liu Hong-Xiang
1 Regenerative Bioscience Center, University of Georgia , Athens, Georgia .
2 Department of Animal and Dairy Science, College of Agricultural and Environmental Sciences, University of Georgia , Athens, Georgia .
Tissue Eng Part C Methods. 2016 Apr;22(4):332-7. doi: 10.1089/ten.TEC.2015.0377. Epub 2016 Jan 25.
Molecular labeling in whole-mount tissues provides an efficient way to obtain general information about the formation, maintenance, degeneration, and regeneration of many organs and tissues. However, labeling of lingual taste buds in whole tongue tissues in adult mice has been problematic because of the strong permeability barrier of the tongue epithelium. In this study, we present a simple method for labeling taste buds in the intact tongue epithelial sheet of an adult mouse. Following intralingual protease injection and incubation, immediate fixation of the tongue on mandible in 4% paraformaldehyde enabled the in situ shape of the tongue epithelium to be well maintained after peeling. The peeled epithelium was accessible to taste bud labeling with a pan-taste cell marker, keratin 8, and a type II taste cell marker, α-gustducin, in all three types of taste papillae, that is, fungiform, foliate, and circumvallate. Overnight incubation of tongue epithelial sheets with primary and secondary antibodies was sufficient for intense labeling of taste buds with both fluorescent and DAB visualizations. Labeled individual taste buds were easy to identify and quantify. This protocol provides an efficient way for phenotypic analyses of taste buds, especially regarding distribution pattern and number.
全组织分子标记为获取有关许多器官和组织的形成、维持、退化及再生的一般信息提供了一种有效方法。然而,由于舌上皮具有强大的渗透屏障,成年小鼠全舌组织中舌味蕾的标记一直存在问题。在本研究中,我们提出了一种在成年小鼠完整舌上皮片中标记味蕾的简单方法。经舌内蛋白酶注射和孵育后,将舌立即固定于下颌骨上并置于4%多聚甲醛中,使得舌上皮在剥离后能够很好地保持原位形态。用泛味细胞标记物角蛋白8和II型味细胞标记物α - 味导素对剥离的上皮进行味蕾标记时,在所有三种类型的味乳头(即菌状乳头、叶状乳头和轮廓乳头)中均能实现。舌上皮片与一抗和二抗过夜孵育足以通过荧光和DAB显色对味蕾进行强烈标记。标记的单个味蕾易于识别和定量。该方案为味蕾的表型分析,特别是关于分布模式和数量的分析,提供了一种有效方法。