dc.contributor.author | Norreen-Thorsen, Marthe | |
dc.contributor.author | Struck, Eike Christopher | |
dc.contributor.author | Öling, Sofia Maria | |
dc.contributor.author | Zwahlen, Martin | |
dc.contributor.author | Von Feilitzen, Kalle | |
dc.contributor.author | Odeberg, Jacob | |
dc.contributor.author | Lindskog, Cecilia | |
dc.contributor.author | Pontén, Fredrik | |
dc.contributor.author | Uhlén, Mathias | |
dc.contributor.author | Dusart, Philip James | |
dc.contributor.author | Butler, Lynn | |
dc.date.accessioned | 2022-11-15T07:51:22Z | |
dc.date.available | 2022-11-15T07:51:22Z | |
dc.date.issued | 2022-07-12 | |
dc.description.abstract | 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. | en_US |
dc.identifier.citation | Norreen-Thorsen, Struck, Öling, Zwahlen, Von Feilitzen, Odeberg, Lindskog, Pontén, Uhlén, Dusart, Butler. A human adipose tissue cell-type transcriptome atlas. Cell reports. 2022;40(2) | en_US |
dc.identifier.cristinID | FRIDAID 2058418 | |
dc.identifier.doi | 10.1016/j.celrep.2022.111046 | |
dc.identifier.issn | 2211-1247 | |
dc.identifier.uri | https://hdl.handle.net/10037/27364 | |
dc.language.iso | eng | en_US |
dc.publisher | Elsevier | en_US |
dc.relation.ispartof | Norreen-Thorsen, M. (2023). The identification of cell type defining genes across human tissues and the functional study of the endothelial adhesion G protein-coupled receptor L4. (Doctoral thesis). <a href=https://hdl.handle.net/10037/29399>https://hdl.handle.net/10037/29399</a> | |
dc.relation.ispartof | Struck, E.C. (2023). The Endothelial Cell Response to Inflammation, the Functional Role of the Endothelial-enriched Protein KANK3 and the Adipose Tissue Transcriptome. (Doctoral thesis). <a href=https://hdl.handle.net/10037/31501>https://hdl.handle.net/10037/31501</a>. | |
dc.relation.journal | Cell reports | |
dc.rights.accessRights | openAccess | en_US |
dc.rights.holder | Copyright 2022 The Author(s) | en_US |
dc.rights.uri | https://creativecommons.org/licenses/by/4.0 | en_US |
dc.rights | Attribution 4.0 International (CC BY 4.0) | en_US |
dc.title | A human adipose tissue cell-type transcriptome atlas | en_US |
dc.type.version | publishedVersion | en_US |
dc.type | Journal article | en_US |
dc.type | Tidsskriftartikkel | en_US |
dc.type | Peer reviewed | en_US |