Evidence map›Paper›PMID 40263573›Full record

ReviewNature cell biology2025

Effects of embryonic origin, tissue cues and pathological signals on fibroblast diversity in humans.

Marta Torregrossa, Lindsay Davies, Machens Hans-Günther, Jan C Simon, Sandra Franz, Yuval Rinkevich

Abstract readReview
PubMed Publisher
In one paragraph

Review in Nature cell biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
–field-weighted citation impact
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

9 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. May In focus in HCB.Histochemistry and cell biology · 2025
    Article
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

6 authors.

Marta TorregrossaDepartment of Dermatology, Venereology and Allergology, Leipzig University Medical Faculty, Leipzig, Germany.
Lindsay DaviesDepartment of Microbiology, Tumor and Cell Biology, Karolinska Institute, Stockholm, Sweden.
Machens Hans-GüntherDepartment for Plastic Surgery and Hand Surgery, Klinikum Rechts der Isar, School of Medicine, Technical University of Munich, Munich, Germany.
Jan C SimonDepartment of Dermatology, Venereology and Allergology, Leipzig University Medical Faculty, Leipzig, Germany.
Sandra Franz *Department of Dermatology, Venereology and Allergology, Leipzig University Medical Faculty, Leipzig, Germany. sandra.franz@medizin.uni-leipzig.de.ORCID http://orcid.org/0000-0002-3449-2723
Yuval Rinkevich *Chinese Institutes for Medical Research, Beijing, China. yuval.rinkevich@cimrbj.ac.cn.

Funding

Deutsche Forschungsgemeinschaft (German Research Foundation) FR2671/5-1
6 · The paper itself

Abstract

Fibroblasts, once perceived as a uniform cell type, are now recognized as a mosaic of distinct populations with specialized roles in tissue homeostasis and pathology. Here we provide a global overview of the expanding compendium of fibroblast cell types and states, their diverse lineage origins and multifaceted functions across various human organs. By integrating insights from developmental biology, lineage tracing and single-cell technologies, we highlight the complex nature of fibroblasts. We delve into their origination from embryonic mesenchyme and tissue-resident populations, elucidating lineage-specific behaviours in response to physiological cues. Furthermore, we highlight the pivotal role of fibroblasts in orchestrating tissue repair, connective tissue remodelling and immune modulation across diverse pathologies. This knowledge is essential to develop novel fibroblast-targeted therapies to restore steady-state fibroblast function and advance regenerative medicine strategies across multiple diseases.

Indexed as

Cell LineageFibroblastsAnimalsCell DifferentiationHumansSignal Transduction

Identifiers

PMID40263573

What Socratic holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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 Socratic graph.