Center for Advanced Tissue Imaging, Laboratory of Immune System Biology, National Institute of Allergy and Infectious Diseases, NIH, Bethesda, MD 20892;
Lymphocyte Biology Section, Laboratory of Immune System Biology, National Institute of Allergy and Infectious Diseases, NIH, Bethesda, MD 20892.
Proc Natl Acad Sci U S A. 2020 Dec 29;117(52):33455-33465. doi: 10.1073/pnas.2018488117. Epub 2020 Dec 21.
The diverse composition of mammalian tissues poses challenges for understanding the cell-cell interactions required for organ homeostasis and how spatial relationships are perturbed during disease. Existing methods such as single-cell genomics, lacking a spatial context, and traditional immunofluorescence, capturing only two to six molecular features, cannot resolve these issues. Imaging technologies have been developed to address these problems, but each possesses limitations that constrain widespread use. Here we report a method that overcomes major impediments to highly multiplex tissue imaging. "Iterative bleaching extends multiplexity" (IBEX) uses an iterative staining and chemical bleaching method to enable high-resolution imaging of >65 parameters in the same tissue section without physical degradation. IBEX can be employed with various types of conventional microscopes and permits use of both commercially available and user-generated antibodies in an "open" system to allow easy adjustment of staining panels based on ongoing marker discovery efforts. We show how IBEX can also be used with amplified staining methods for imaging strongly fixed tissues with limited epitope retention and with oligonucleotide-based staining, allowing potential cross-referencing between flow cytometry, cellular indexing of transcriptomes and epitopes by sequencing, and IBEX analysis of the same tissue. To facilitate data processing, we provide an open-source platform for automated registration of iterative images. IBEX thus represents a technology that can be rapidly integrated into most current laboratory workflows to achieve high-content imaging to reveal the complex cellular landscape of diverse organs and tissues.
哺乳动物组织的多样化组成对理解维持器官稳态所需的细胞间相互作用以及在疾病过程中空间关系如何受到干扰提出了挑战。现有的方法,如单细胞基因组学,缺乏空间背景,而传统的免疫荧光技术只能捕捉到两个到六个分子特征,无法解决这些问题。已经开发出成像技术来解决这些问题,但每种技术都存在限制,限制了其广泛应用。在这里,我们报告了一种克服高度多重组织成像主要障碍的方法。“迭代漂白扩展多重性”(IBEX)使用迭代染色和化学漂白方法,在同一组织切片中实现>65 个参数的高分辨率成像,而不会造成物理降解。IBEX 可以与各种类型的传统显微镜一起使用,并允许在“开放”系统中使用商业上可获得的和用户生成的抗体,以根据正在进行的标记物发现工作轻松调整染色面板。我们展示了如何将 IBEX 与放大染色方法结合使用,以对具有有限表位保留的强固定组织进行成像,并与基于寡核苷酸的染色结合使用,允许在流式细胞术、通过测序对转录物和表位进行细胞索引以及对同一组织进行 IBEX 分析之间进行潜在的交叉引用。为了便于数据处理,我们提供了一个用于迭代图像自动配准的开源平台。因此,IBEX 代表了一种可以快速集成到大多数当前实验室工作流程中的技术,以实现高内涵成像,揭示各种器官和组织的复杂细胞景观。