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A human adipose tissue cell-type transcriptome atlas

The importance of defining cell-type-specific genes is well acknowledged. Technological advances facilitate high-resolution sequencing of single cells, but practical challenges remain. Adipose tissue is composed primarily of adipocytes, large buoyant cells requiring extensive, artefact-generating pr...

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Published in:Cell reports (Cambridge) 2022, Vol.40 (2), p.111046-111046, Article 111046
Main Authors: Norreen-Thorsen, Marthe, Struck, Eike Christopher, Öling, Sofia, Zwahlen, Martin, Von Feilitzen, Kalle, Odeberg, Jacob, Lindskog, Cecilia, Pontén, Fredrik, Uhlén, Mathias, Dusart, Philip James, Butler, Lynn Marie
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container_title Cell reports (Cambridge)
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creator Norreen-Thorsen, Marthe
Struck, Eike Christopher
Öling, Sofia
Zwahlen, Martin
Von Feilitzen, Kalle
Odeberg, Jacob
Lindskog, Cecilia
Pontén, Fredrik
Uhlén, Mathias
Dusart, Philip James
Butler, Lynn Marie
description The importance of defining cell-type-specific genes is well acknowledged. Technological advances facilitate high-resolution sequencing of single cells, but practical challenges remain. Adipose tissue is composed primarily of adipocytes, large buoyant cells requiring extensive, artefact-generating processing for separation and analysis. Thus, adipocyte data are frequently absent from single-cell RNA sequencing (scRNA-seq) datasets, despite being the primary functional cell type. Here, we decipher cell-type-enriched transcriptomes from unfractionated human adipose tissue RNA-seq data. We profile all major constituent cell types, using 527 visceral adipose tissue (VAT) or 646 subcutaneous adipose tissue (SAT) samples, identifying over 2,300 cell-type-enriched transcripts. Sex-subset analysis uncovers a panel of male-only cell-type-enriched genes. By resolving expression profiles of genes differentially expressed between SAT and VAT, we identify mesothelial cells as the primary driver of this variation. This study provides an accessible method to profile cell-type-enriched transcriptomes using bulk RNA-seq, generating a roadmap for adipose tissue biology. [Display omitted] •Uses publicly available adipose tissue bulk RNA-seq data from two human fat depots•Enriched genes in 10 cell types profiled using an integrative correlation analysis•Comparative analysis identifies depot- and sex-specific cell-type-enriched genes•Method circumvents technical challenges with adipose tissue scRNA-seq analysis Norreen-Thorsen et al. use an integrative correlation analysis of human adipose tissue RNA-seq data, identifying >2,000 cell-type-enriched coding and non-coding transcripts. Comparative analyses highlight transcripts with visceral and subcutaneous depot-specific and/or sex-specific cell-type enrichment. The method allows profiling of adipocytes, whose physical characteristics make analysis with other methods challenging.
doi_str_mv 10.1016/j.celrep.2022.111046
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2211-1247
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source BACON - Elsevier - GLOBAL_SCIENCEDIRECT-OPENACCESS; NORA - Norwegian Open Research Archives
subjects adipocytes
adipose tissue
cell profiling
Medicin och hälsovetenskap
RNA-seq
title A human adipose tissue cell-type transcriptome atlas
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