Open-ST: High-resolution spatial transcriptomics in 3D

Marie Schott(Max Delbrück Center), Daniel León-Periñán(Max Delbrück Center), Elena Splendiani(Max Delbrück Center), Leon Strenger(Max Delbrück Center), Jan Robin Licha(Max Delbrück Center), Tancredi Massimo Pentimalli(Max Delbrück Center), Simon Schallenberg(Humboldt-Universität zu Berlin), Jonathan Alles(Max Delbrück Center), Sarah Samut Tagliaferro(Max Delbrück Center), Anastasiya Boltengagen(Max Delbrück Center), Sebastian Ehrig(Max Delbrück Center), Stefano Abbiati(Max Delbrück Center), Steffen Dommerich(Humboldt-Universität zu Berlin), Massimiliano Pagani(University of Milan), Elisabetta Ferretti(Sapienza University of Rome), Giuseppe Macino(Max Delbrück Center), Nikos Karaiskos(Max Delbrück Center), Nikolaus Rajewsky(Max Delbrück Center)
bioRxiv (Cold Spring Harbor Laboratory)
December 23, 2023
Cited by 26Open Access
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Abstract

Abstract Spatial transcriptomics (ST) methods have been developed to unlock molecular mechanisms underlying tissue development, homeostasis, or disease. However, there is a need for easy-to-use, high-resolution, cost-efficient, and 3D-scalable methods. Here, we report Open-ST, a sequencing-based, open-source experimental and computational resource to address these challenges and to study the molecular organization of tissues in 3D. In mouse brain, Open-ST captured transcripts at subcellular resolution and reconstructed cell types. In primary tumor and patient-matched healthy/metastatic lymph nodes, Open-ST captured the diversity of immune, stromal and tumor populations in space. Distinct cell states were organized around cell-cell communication hotspots in the tumor, but not the metastasis. Strikingly, the 3D reconstruction and multimodal analysis of the metastatic lymph node revealed spatially contiguous structures not visible in 2D and potential biomarkers precisely at the 3D tumor/lymph node boundary. We anticipate Open-ST to accelerate the identification of spatial molecular mechanisms in 2D and 3D.


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