Fibroblast atlas: Shared and specific cell types across tissues

Understanding the heterogeneity of fibroblasts depends on decoding the complexity of cell subtypes, their origin, distribution, and interactions with other cells. Here, we integrated 249,156 fibroblasts from 73 studies across 10 tissues to present a single-cell atlas of fibroblasts. We provided a high-resolution classification of 18 fibroblast subtypes. In particular, we revealed a previously undescribed cell population, TSPAN8<sup>+</sup> chromatin remodeling fibroblasts, characterized by high expression of genes with functions related to histone modification and chromatin remodeling. Moreover, TSPAN8<sup>+</sup> chromatin remodeling fibroblasts were detectable in spatial transcriptome data and multiplexed immunofluorescence assays. Compared with other fibroblast subtypes, TSPAN8<sup>+</sup> chromatin remodeling fibroblasts exhibited higher scores in cell differentiation and resident fibroblast, mainly interacting with endothelial cells and T cells through ligand <i>VEGFA</i> and receptor <i>F2R</i>, and their presence was associated with poor prognosis. Our analyses comprehensively defined the shared and specific characteristics of fibroblast subtypes across tissues and provided a user-friendly data portal, Fibroblast Atlas.

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Publication Details

Journal
Science Advances
Published
2025-04-02
DOI
https://doi.org/10.1126/sciadv.ado0173
Citations
18
Primary Topic
Single-cell and spatial transcriptomics
Type
article
Field-Weighted Citation Impact
14.51
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article

Fibroblast atlas: Shared and specific cell types across tissues

Nan Zhang, Mingyue Liu, Yunyan Gu, Bo Chen et al.
18 citations
Science Advances
Single-cell and spatial transcriptomics
14.51
article

Fibroblast atlas: Shared and specific cell types across tissues

Nan Zhang, Mingyue Liu, Yunyan Gu, Bo Chen, Huiming Han, Kai Xiong, Songmei Zhai, Kaidong Liu, Yanrui Cui, Xingyang Shi, Shaocong Sang, Erliang Guo
article en
18 citations

Abstract

Understanding the heterogeneity of fibroblasts depends on decoding the complexity of cell subtypes, their origin, distribution, and interactions with other cells. Here, we integrated 249,156 fibroblasts from 73 studies across 10 tissues to present a single-cell atlas of fibroblasts. We provided a high-resolution classification of 18 fibroblast subtypes. In particular, we revealed a previously undescribed cell population, TSPAN8<sup>+</sup> chromatin remodeling fibroblasts, characterized by high expression of genes with functions related to histone modification and chromatin remodeling. Moreover, TSPAN8<sup>+</sup> chromatin remodeling fibroblasts were detectable in spatial transcriptome data and multiplexed immunofluorescence assays. Compared with other fibroblast subtypes, TSPAN8<sup>+</sup> chromatin remodeling fibroblasts exhibited higher scores in cell differentiation and resident fibroblast, mainly interacting with endothelial cells and T cells through ligand <i>VEGFA</i> and receptor <i>F2R</i>, and their presence was associated with poor prognosis. Our analyses comprehensively defined the shared and specific characteristics of fibroblast subtypes across tissues and provided a user-friendly data portal, Fibroblast Atlas.

Science AdvancesVol. 11(14)
Harbin Medical University (CN), Third Affiliated Hospital of Harbin Medical University (CN)
No poverty
Openalex Percentile: Top 1%
Single-cell and spatial transcriptomics
14.51
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