Spatially resolved single-cell RNA sequencing (scRNAseq) is a powerful approach for inferring connections between a cell's identity and its position in a tissue. We recently combined scRNAseq with spatially mapped landmark genes to infer the expression zonation of hepatocytes. However, determining zonation of small cells with low mRNA content, or without highly expressed landmark genes, remains challenging. Here we used paired-cell sequencing, in which mRNA from pairs of attached mouse cells were sequenced and gene expression from one cell type was used to infer the pairs' tissue coordinates. We applied this method to pairs of hepatocytes and liver endothelial cells (LECs). Using the spatial information from hepatocytes, we reconstructed LEC zonation and extracted a landmark gene panel that we used to spatially map LEC scRNAseq data. Our approach revealed the expression of both Wnt ligands and the Dkk3 Wnt antagonist in distinct pericentral LEC sub-populations. This approach can be used to reconstruct spatial expression maps of non-parenchymal cells in other tissues.
Journal article
Paired-cell sequencing enables spatial gene expression mapping of liver endothelial cells
Nature Biotechnology, Vol.36(10), pp.962-+
Oct/2018
Abstract
Details
- Title
- Paired-cell sequencing enables spatial gene expression mapping of liver endothelial cells
- Creators
- Keren Bahar Halpern (null) - 972WIS_INST___122Rom Shenhav (null) - 972WIS_INST___122Hassan Massalha (null) - 972WIS_INST___122Beata Toth (null) - The Weizmann Institute of ScienceAdi Egozi (null) - 972WIS_INST___122Efi E. Massasa (null) - The Weizmann Institute of ScienceChiara Medgalia (null) - The Weizmann Institute of ScienceEyal David (null) - The Weizmann Institute of ScienceAmir Giladi (null) - 972WIS_INST___120Andreas E. Moor (null) - 972WIS_INST___122Ziv Porat (null) - 972WIS_INST___113Ido Amit (null) - 972WIS_INST___120Shalev Itzkovitz (Corresponding Author) - 972WIS_INST___122
- Resource Type
- Journal article
- Publication Details
- Nature Biotechnology, Vol.36(10), pp.962-+; Oct/2018
- Number of pages
- 12
- Language
- English
- DOI
- https://doi.org/10.1038/nbt.4231
- Grant note
- We thank M. Kolesnikov and S. Jung (Weizmann Institute) for the C57BL/6-Actb-DsRed.T3 mice and D. Jaitin (Weizmann Institute) for the C57BL/6-Tg(CAG-EGFP) mice. S.I. is supported by the Henry Chanoch Krenter Institute for Biomedical Imaging and Genomics, The Leir Charitable Foundations, Richard Jakubskind Laboratory of Systems Biology, Cymerman-Jakubskind Prize, The Lord Sieff of Brimpton Memorial Fund, the I-CORE program of the Planning and Budgeting Committee and the Israel Science Foundation (grants 1902/ 12 and 1796/12), the Israel Science Foundation grant No. 1486/16, the EMBO Young Investigator Program and the European Research Council under the European Union's Seventh Framework Programme (FP7/2007-2013)/ERC grant agreement number 335122, the Bert L. and N. Kuggie Vallee Foundation and the Howard Hughes Medical Institute (HHMI) international research scholar award. S.I. is the incumbent of the Philip Harris and Gerald Ronson Career Development Chair.
- Record Identifier
- 993268210103596
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