Nature Communications (Mar 2024)

Mapping human tissues with highly multiplexed RNA in situ hybridization

  • Kian Kalhor,
  • Chien-Ju Chen,
  • Ho Suk Lee,
  • Matthew Cai,
  • Mahsa Nafisi,
  • Richard Que,
  • Carter R. Palmer,
  • Yixu Yuan,
  • Yida Zhang,
  • Xuwen Li,
  • Jinghui Song,
  • Amanda Knoten,
  • Blue B. Lake,
  • Joseph P. Gaut,
  • C. Dirk Keene,
  • Ed Lein,
  • Peter V. Kharchenko,
  • Jerold Chun,
  • Sanjay Jain,
  • Jian-Bing Fan,
  • Kun Zhang

DOI
https://doi.org/10.1038/s41467-024-46437-y
Journal volume & issue
Vol. 15, no. 1
pp. 1 – 17

Abstract

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Abstract 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 20 healthy and pathological cell states, and identified diseased niches enriched in transcriptionally altered epithelial cells and myofibroblasts.