Evidence mapPaperPMID 39768155Full record

ArticleCells2024

The Role of Activated Stromal Cells in Fibrotic Foci Formation and Reversion.

Nataliya Andreevna Basalova, Maksim Alexandrovich Vigovskiy, Vladimir Sergeevich Popov, Evgeniya Alexandrovna Lagereva, Olga Alexandrovna Grigorieva, Anastasia Yuryevna Efimenko

Abstract read
In one paragraph

Article in Cells, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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.

Nataliya Andreevna BasalovaCentre for Regenerative Medicine, Medical Research and Educational Institute, Lomonosov Moscow State University, 119192 Moscow, Russia.
Maksim Alexandrovich VigovskiyCentre for Regenerative Medicine, Medical Research and Educational Institute, Lomonosov Moscow State University, 119192 Moscow, Russia.ORCID 0000-0003-2103-8158
Vladimir Sergeevich PopovCentre for Regenerative Medicine, Medical Research and Educational Institute, Lomonosov Moscow State University, 119192 Moscow, Russia.ORCID 0000-0002-5039-7152
Evgeniya Alexandrovna LagerevaCentre for Regenerative Medicine, Medical Research and Educational Institute, Lomonosov Moscow State University, 119192 Moscow, Russia.ORCID 0000-0002-6701-0487
Olga Alexandrovna GrigorievaCentre for Regenerative Medicine, Medical Research and Educational Institute, Lomonosov Moscow State University, 119192 Moscow, Russia.
Anastasia Yuryevna EfimenkoCentre for Regenerative Medicine, Medical Research and Educational Institute, Lomonosov Moscow State University, 119192 Moscow, Russia.ORCID 0000-0002-0696-1369

Funding

Russian Science Foundation 23-15-00198
6 · The paper itself

Abstract

Fibrotic focus is a pivotal morphofunctional unit in developing fibrosis in various tissues. For most fibrotic diseases, including progressive forms, the foci are considered unable to remodel and contribute to the worsening of prognosis. Unfortunately, the dynamics of the fibrotic focus formation and resolution remains understudied. A number of data suggest that the key cell type for focus formation are activated stromal cells marked by fibroblast activated protein alpha (FAPα) due to their high capacity for extracellular matrix (ECM) remodeling. We evaluated the dynamics of fibrotic focus formation and the contribution of the main cell types, including FAPα+ cells, in this process using a murine model of bleomycin-induced lung fibrosis. We revealed the very early appearance of FAPα+ cells in lungs after injury and assumed their important involvement to the myofibroblast pool formation. During the first month after bleomycin administration, FAPα+ cells colocalize with CD206+ M2 macrophages. Interestingly, during the reversion stage, we unexpectedly observed the specific structured foci formed by CD90+FAPα+ cells, which we suggested calling "remodeling foci". Our findings highlight the crucial role of activated stromal cells in fibrosis initiation, progression, and reversion and provide emerging issues regarding the novel targets for antifibrotic therapy.

Indexed as

BleomycinStromal CellsAnimalsDisease Models, AnimalEndopeptidasesExtracellular MatrixFibroblast Activation Protein AlphaFibrosisHumansLungMacrophagesMembrane ProteinsMiceMice, Inbred C57BLMyofibroblastsPulmonary FibrosisBleomycinEndopeptidasesFibroblast Activation Protein AlphaMembrane Proteinsactivated stromal cellsCD90 (THY-1)FAPαfibroblast activation proteinfibrosismyofibroblasts

Identifiers

PMID39768155
PMCPMC11674712

What Socratic holds

Textmetadata
LicenceCC BY
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.