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DestVI identifies continuums of cell types in spatial transcriptomics data
The function of mammalian cells is largely influenced by their tissue microenvironment. Advances in spatial transcriptomics open the way for studying these important determinants of cellular function by enabling a transcriptome-wide evaluation of gene expression in situ. A critical limitation of the...
Autores principales: | , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9756396/ https://www.ncbi.nlm.nih.gov/pubmed/35449415 http://dx.doi.org/10.1038/s41587-022-01272-8 |
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author | Lopez, Romain Li, Baoguo Keren-Shaul, Hadas Boyeau, Pierre Kedmi, Merav Pilzer, David Jelinski, Adam David, Eyal Wagner, Allon Addadi, Yoseph Elhanani, Ofer Fatelevich, Michal Yankielowicz-Keren, Leeat Golani, Ofra Ronchese, Franca Jordan, Michael I. Amit, Ido Yosef, Nir |
author_facet | Lopez, Romain Li, Baoguo Keren-Shaul, Hadas Boyeau, Pierre Kedmi, Merav Pilzer, David Jelinski, Adam David, Eyal Wagner, Allon Addadi, Yoseph Elhanani, Ofer Fatelevich, Michal Yankielowicz-Keren, Leeat Golani, Ofra Ronchese, Franca Jordan, Michael I. Amit, Ido Yosef, Nir |
author_sort | Lopez, Romain |
collection | PubMed |
description | The function of mammalian cells is largely influenced by their tissue microenvironment. Advances in spatial transcriptomics open the way for studying these important determinants of cellular function by enabling a transcriptome-wide evaluation of gene expression in situ. A critical limitation of the current technologies, however, is that their resolution is limited to niches (spots) of sizes well beyond that of a single cell, thus providing measurements for cell aggregates which may mask critical interactions between neighboring cells of different types. While joint analysis with single-cell RNA-sequencing (scRNA-seq) can be leveraged to alleviate this problem, current analyses are limited to a discrete view of cell type proportion inside every spot. This limitation becomes critical in the common case where, even within a cell type, there is a continuum of cell states that cannot be clearly demarcated but reflects important differences in the way cells function and interact with their surroundings. To address this, we developed Deconvolution of Spatial Transcriptomics profiles using Variational Inference (DestVI), a probabilistic method for multi-resolution analysis for spatial transcriptomics that explicitly models continuous variation within cell types. Using simulations, we demonstrate that DestVI is capable of providing higher resolution compared to the existing methods and that it can estimate gene expression by every cell type inside every spot. We then introduce an automated pipeline that uses DestVI for analysis of single tissue sections and comparison between tissues. We apply this pipeline to study immune crosstalk within lymph nodes following infection and explore the spatial organization of a mouse tumor model. In both cases, we demonstrate that DestVI can provide a high resolution and accurate spatial characterization of the cellular organization of these tissues, and that it is capable of identifying important cell-type-specific changes in gene expression - between different tissue regions or between conditions. DestVI is available as an open-source software package in the scvi-tools codebase (https://scvi-tools.org). |
format | Online Article Text |
id | pubmed-9756396 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
record_format | MEDLINE/PubMed |
spelling | pubmed-97563962022-12-16 DestVI identifies continuums of cell types in spatial transcriptomics data Lopez, Romain Li, Baoguo Keren-Shaul, Hadas Boyeau, Pierre Kedmi, Merav Pilzer, David Jelinski, Adam David, Eyal Wagner, Allon Addadi, Yoseph Elhanani, Ofer Fatelevich, Michal Yankielowicz-Keren, Leeat Golani, Ofra Ronchese, Franca Jordan, Michael I. Amit, Ido Yosef, Nir Nat Biotechnol Article The function of mammalian cells is largely influenced by their tissue microenvironment. Advances in spatial transcriptomics open the way for studying these important determinants of cellular function by enabling a transcriptome-wide evaluation of gene expression in situ. A critical limitation of the current technologies, however, is that their resolution is limited to niches (spots) of sizes well beyond that of a single cell, thus providing measurements for cell aggregates which may mask critical interactions between neighboring cells of different types. While joint analysis with single-cell RNA-sequencing (scRNA-seq) can be leveraged to alleviate this problem, current analyses are limited to a discrete view of cell type proportion inside every spot. This limitation becomes critical in the common case where, even within a cell type, there is a continuum of cell states that cannot be clearly demarcated but reflects important differences in the way cells function and interact with their surroundings. To address this, we developed Deconvolution of Spatial Transcriptomics profiles using Variational Inference (DestVI), a probabilistic method for multi-resolution analysis for spatial transcriptomics that explicitly models continuous variation within cell types. Using simulations, we demonstrate that DestVI is capable of providing higher resolution compared to the existing methods and that it can estimate gene expression by every cell type inside every spot. We then introduce an automated pipeline that uses DestVI for analysis of single tissue sections and comparison between tissues. We apply this pipeline to study immune crosstalk within lymph nodes following infection and explore the spatial organization of a mouse tumor model. In both cases, we demonstrate that DestVI can provide a high resolution and accurate spatial characterization of the cellular organization of these tissues, and that it is capable of identifying important cell-type-specific changes in gene expression - between different tissue regions or between conditions. DestVI is available as an open-source software package in the scvi-tools codebase (https://scvi-tools.org). 2022-09 2022-04-21 /pmc/articles/PMC9756396/ /pubmed/35449415 http://dx.doi.org/10.1038/s41587-022-01272-8 Text en http://www.nature.com/authors/editorial_policies/license.html#termsUsers may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms |
spellingShingle | Article Lopez, Romain Li, Baoguo Keren-Shaul, Hadas Boyeau, Pierre Kedmi, Merav Pilzer, David Jelinski, Adam David, Eyal Wagner, Allon Addadi, Yoseph Elhanani, Ofer Fatelevich, Michal Yankielowicz-Keren, Leeat Golani, Ofra Ronchese, Franca Jordan, Michael I. Amit, Ido Yosef, Nir DestVI identifies continuums of cell types in spatial transcriptomics data |
title | DestVI identifies continuums of cell types in spatial transcriptomics data |
title_full | DestVI identifies continuums of cell types in spatial transcriptomics data |
title_fullStr | DestVI identifies continuums of cell types in spatial transcriptomics data |
title_full_unstemmed | DestVI identifies continuums of cell types in spatial transcriptomics data |
title_short | DestVI identifies continuums of cell types in spatial transcriptomics data |
title_sort | destvi identifies continuums of cell types in spatial transcriptomics data |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9756396/ https://www.ncbi.nlm.nih.gov/pubmed/35449415 http://dx.doi.org/10.1038/s41587-022-01272-8 |
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