{"title":"Hybridization Chain Reaction for mRNA Localization in Single Cells from Mouse and Human Cryosections.","authors":"Aaron A May-Zhang, Joseph T Benthal, E Michelle Southard-Smith","doi":"10.1002/cpz1.439","DOIUrl":null,"url":null,"abstract":"<p><p>In situ hybridization has been a robust method for detection of mRNA expression in whole-mount samples or tissue sections for more than 50 years. Recent technical advances for in situ hybridization have incorporated oligo-based probes that attain greater tissue penetration and signal amplification steps with restricted localization for visualization of specific mRNAs within single cells. One such method is third-generation in situ hybridization chain reaction (V3HCR). Here, we report an optimized protocol for V3HCR detection of gene expression using sectioned frozen tissues from mouse and human on microscope slides. Our methods and modifications for cryosectioning, tissue fixation, and processing over a three-day V3HCR protocol are detailed along with recommendations for aliquoting and storing V3HCR single-stranded DNA probes and hairpin amplifiers. In addition, we describe a method for blocking background signal from lipofuscin, a highly autofluorescent material that is widespread in human neurons and often complicates imaging efforts. After testing multiple strategies for reduction of lipofuscin, we determined that application of a lipofuscin quencher dye is compatible with V3HCR, in contrast to other methods like cupric sulfate quenching or Sudan Black B blocking that cause V3HCR signal loss. This adaptation enables application of V3HCR for in situ detection of gene expression in human neuronal populations that are otherwise problematic due to lipofuscin autofluorescence. © 2022 Wiley Periodicals LLC. Basic Protocol: Mouse and human fresh-frozen tissue in situ hybridization chain reaction on microscope slides Support Protocol: Aliquoting of HCR probes and hairpins.</p>","PeriodicalId":11174,"journal":{"name":"Current Protocols","volume":"2 5","pages":"e439"},"PeriodicalIF":0.0000,"publicationDate":"2022-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9202517/pdf/nihms-1800310.pdf","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current Protocols","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1002/cpz1.439","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
In situ hybridization has been a robust method for detection of mRNA expression in whole-mount samples or tissue sections for more than 50 years. Recent technical advances for in situ hybridization have incorporated oligo-based probes that attain greater tissue penetration and signal amplification steps with restricted localization for visualization of specific mRNAs within single cells. One such method is third-generation in situ hybridization chain reaction (V3HCR). Here, we report an optimized protocol for V3HCR detection of gene expression using sectioned frozen tissues from mouse and human on microscope slides. Our methods and modifications for cryosectioning, tissue fixation, and processing over a three-day V3HCR protocol are detailed along with recommendations for aliquoting and storing V3HCR single-stranded DNA probes and hairpin amplifiers. In addition, we describe a method for blocking background signal from lipofuscin, a highly autofluorescent material that is widespread in human neurons and often complicates imaging efforts. After testing multiple strategies for reduction of lipofuscin, we determined that application of a lipofuscin quencher dye is compatible with V3HCR, in contrast to other methods like cupric sulfate quenching or Sudan Black B blocking that cause V3HCR signal loss. This adaptation enables application of V3HCR for in situ detection of gene expression in human neuronal populations that are otherwise problematic due to lipofuscin autofluorescence. © 2022 Wiley Periodicals LLC. Basic Protocol: Mouse and human fresh-frozen tissue in situ hybridization chain reaction on microscope slides Support Protocol: Aliquoting of HCR probes and hairpins.
小鼠和人单细胞冷冻切片mRNA定位的杂交链式反应。
原位杂交已经是一种强大的方法来检测mRNA表达在全挂载样品或组织切片超过50年。原位杂交的最新技术进步已经纳入了寡基探针,这种探针可以实现更大的组织渗透和信号放大步骤,同时限制了单个细胞内特定mrna的可视化定位。其中一种方法是第三代原位杂交链反应(V3HCR)。在这里,我们报告了一种优化的V3HCR基因表达检测方案,该方案使用小鼠和人的切片冷冻组织在显微镜载玻片上进行检测。我们的方法和修改冷冻切片,组织固定和处理超过三天的V3HCR协议详细介绍了ali引用和存储V3HCR单链DNA探针和发夹放大器的建议。此外,我们描述了一种阻断来自脂褐素的背景信号的方法,脂褐素是一种在人类神经元中广泛存在的高度自荧光材料,通常使成像工作复杂化。在测试了多种减少脂褐素的策略后,我们确定脂褐素猝灭剂染料的应用与V3HCR兼容,而其他方法如硫酸铜淬火或苏丹黑B阻断会导致V3HCR信号丢失。这种适应性使V3HCR能够应用于人类神经元群体中基因表达的原位检测,否则由于脂褐素自身荧光而存在问题。©2022 Wiley期刊有限责任公司基本方案:小鼠和人类新鲜冷冻组织在显微镜载玻片上的原位杂交链反应支持方案:HCR探针和发夹的alicitation。
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