Evidence map›Paper›PMID 34140509›Full record

ArticleNature communications2021

Single-cell RNA-seq reveals fibroblast heterogeneity and increased mesenchymal fibroblasts in human fibrotic skin diseases.

Cheng-Cheng Deng, Yong-Fei Hu, Ding-Heng Zhu, Qing Cheng, Jing-Jing Gu, Qing-Lan Feng, Li-Xue Zhang, Ying-Ping Xu, Dong Wang, Zhili Rong and 1 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 299 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
299citing papers in PubMed, 2 pooled it
58.0field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

299 citing papers in PubMed, 2 syntheses or guidelines pooled it, 437 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Trial
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  5. Review
  6. Review
  7. Article
  8. Article
  9. Identification and characterization of POSTNJournal of orthopaedic translation · 2026
    Article
  10. Article
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  12. A practical toolbox for modelling fibrosis in vitro.Nature biomedical engineering · 2026
    Review
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  20. Collagen-producing eye cell atlas reveals distinct fibroblast fates in early injury vs. fibrotic subretinal disease.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article

239 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors at 2 institutions in 2 countries.

Cheng-Cheng Deng *Dermatology Hospital, Southern Medical University, Guangzhou, China.ORCID 0000-0001-9616-1607
Yong-Fei Hu *Dermatology Hospital, Southern Medical University, Guangzhou, China.ORCID 0000-0002-9288-0994
Ding-Heng Zhu *Dermatology Hospital, Southern Medical University, Guangzhou, China.
Qing ChengDermatology Hospital, Southern Medical University, Guangzhou, China.
Jing-Jing GuDermatology Hospital, Southern Medical University, Guangzhou, China.
Qing-Lan FengDermatology Hospital, Southern Medical University, Guangzhou, China.
Li-Xue ZhangDermatology Hospital, Southern Medical University, Guangzhou, China.
Ying-Ping XuDermatology Hospital, Southern Medical University, Guangzhou, China.
Dong WangDermatology Hospital, Southern Medical University, Guangzhou, China.ORCID 0000-0002-6860-6864
Zhili RongDermatology Hospital, Southern Medical University, Guangzhou, China. rongzhili@smu.edu.cn.ORCID 0000-0002-1699-7074
Bin YangDermatology Hospital, Southern Medical University, Guangzhou, China. yangbin1@smu.edu.cn.ORCID 0000-0002-7155-6079
Southern Medical University · CNMinistry of Education · BN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Fibrotic skin disease represents a major global healthcare burden, characterized by fibroblast hyperproliferation and excessive accumulation of extracellular matrix. Fibroblasts are found to be heterogeneous in multiple fibrotic diseases, but fibroblast heterogeneity in fibrotic skin diseases is not well characterized. In this study, we explore fibroblast heterogeneity in keloid, a paradigm of fibrotic skin diseases, by using single-cell RNA-seq. Our results indicate that keloid fibroblasts can be divided into 4 subpopulations: secretory-papillary, secretory-reticular, mesenchymal and pro-inflammatory. Interestingly, the percentage of mesenchymal fibroblast subpopulation is significantly increased in keloid compared to normal scar. Functional studies indicate that mesenchymal fibroblasts are crucial for collagen overexpression in keloid. Increased mesenchymal fibroblast subpopulation is also found in another fibrotic skin disease, scleroderma, suggesting this is a broad mechanism for skin fibrosis. These findings will help us better understand skin fibrotic pathogenesis, and provide potential targets for fibrotic disease therapies.

Indexed as

Cell Adhesion MoleculesCollagenExtracellular MatrixFibroblastsGene Expression RegulationGene OntologyHumansKeloidLigandsMesodermRNA-SeqScleroderma, SystemicSingle-Cell AnalysisSkin DiseasesCell Adhesion MoleculesCollagenLigandsPOSTN protein, human

Identifiers

PMID34140509
PMCPMC8211847
OpenAlexW3171631195

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.