Department of Bioengineering, University of California San Diego, La Jolla, CA, USA.
Program in Bioinformatics and Systems Biology, University of California San Diego, La Jolla, CA, USA.
Nat Commun. 2024 Mar 20;15(1):2511. doi: 10.1038/s41467-024-46437-y.
In situ transcriptomic techniques promise a holistic view of tissue organization and cell-cell interactions. There has been a surge of multiplexed RNA in situ mapping techniques but their application to human tissues has been limited due to their large size, general lower tissue quality and high autofluorescence. Here we report DART-FISH, a padlock probe-based technology capable of profiling hundreds to thousands of genes in centimeter-sized human tissue sections. We introduce an omni-cell type cytoplasmic stain that substantially improves the segmentation of cell bodies. Our enzyme-free isothermal decoding procedure allows us to image 121 genes in large sections from the human neocortex in <10 h. We successfully recapitulated the cytoarchitecture of 20 neuronal and non-neuronal subclasses. We further performed in situ mapping of 300 genes on a diseased human kidney, profiled >20 healthy and pathological cell states, and identified diseased niches enriched in transcriptionally altered epithelial cells and myofibroblasts.
原位转录组技术有望提供组织整体结构和细胞间相互作用的全景图。目前已经涌现出许多多重 RNA 原位映射技术,但由于其体积较大、组织质量一般较低以及自发荧光较强,这些技术在人类组织中的应用受到限制。在这里,我们报告了 DART-FISH,这是一种基于锁式探针的技术,能够对厘米大小的人体组织切片中的数百到数千个基因进行分析。我们引入了一种全能细胞类型细胞质染色剂,可大大改善细胞体的分割。我们的无酶等温解码程序允许我们在不到 10 小时的时间内对人类新皮层的大片组织进行 121 个基因的成像。我们成功地重现了 20 种神经元和非神经元亚类的细胞结构。我们进一步对 300 个基因在患病人类肾脏上进行了原位映射,分析了 >20 种健康和病理细胞状态,并鉴定出富含转录改变上皮细胞和肌成纤维细胞的病变龛位。