Evidence map›Paper›PMID 42033568›Full record

ArticleTissue engineering and regenerative medicine2026

Intralesional Adipose-Derived Stem Cells Reverse Established Dermal Fibrosis and Modulate Angiogenesis-Related Readouts in a Murine Systemic Sclerosis Model.

Eunji Lee, Yeon Hee Ryu, Su Jin Lee, So Hyun Kwon, Suk-Ho Moon

Abstract read
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Article in Tissue engineering and regenerative medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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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

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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

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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.

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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

5 authors.

Eunji LeeDepartment of Medical Sciences, College of Medicine, The Catholic University of Korea, Seoul, Republic of Korea.
Yeon Hee RyuDepartment of Medical Sciences, College of Medicine, The Catholic University of Korea, Seoul, Republic of Korea.
Su Jin LeeDepartment of Medical Sciences, College of Medicine, The Catholic University of Korea, Seoul, Republic of Korea.
So Hyun KwonDepartment of Medical Sciences, College of Medicine, The Catholic University of Korea, Seoul, Republic of Korea.
Suk-Ho MoonDepartment of Medical Sciences, College of Medicine, The Catholic University of Korea, Seoul, Republic of Korea. nasuko@catholic.ac.kr.ORCID http://orcid.org/0000-0003-1866-2910

Funding

Korea Institute for Advanced Study 23C0124L1Ministry of Health and Welfare HI22C1314
6 · The paper itself

Abstract

backgroundSystemic sclerosis (SSc) is characterized by progressive dermal fibrosis and microvascular dysfunction, and no approved therapy reliably reverses established skin fibrosis or durably restores microvascular perfusion. Adipose-derived stem cells (ASCs) possess anti-fibrotic, immunomodulatory, and vascular-related parameters properties, but their therapeutic impact in a strictly therapeutic (rather than preventive) SSc-like setting remains incompletely defined.

methodsBleomycin-induced systemic sclerosis model was induced in male C57BL/6 mice by daily subcutaneous bleomycin injections (100 μg) into dorsal skin for 28 days. On day 14, mice received a single intralesional injection of ASCs (1 × 10

resultsIntralesional ASC administration significantly attenuated bleomycin-induced dermal fibrosis, reducing dermal thickness (244.0-163.5 μm) and collagen area fraction (87.2-62.8%). Hydroxyproline content decreased from 0.187 to 0.121 μg/mg tissue. ASC treatment also suppressed profibrotic and inflammatory transcripts (α-SMA ~ 3.99-fold, TGF-β1 ~ 6.07-fold, TNF-α ~ 7.48-fold, IL-6 ~ 2.36-fold vs. BLM + PBS) and increased vascular responses transcripts (VEGF ~ 2.65-fold, CD34 ~ 1.28-fold vs. BLM + PBS). ASC co-culture suppressed profibrotic activation of TGF-β1-stimulated fibroblasts, reducing profibrotic expression (α-SMA ~ 2.5-fold, TGF-β1 ~ 3.5 -fold, and COL1A1 ~ 2.7-fold).

conclusionsA single intralesional ASC injection alleviated established bleomycin-induced dermal fibrosis and was associated with vascular-related changes in fibrotic tissue. These effects may involve paracrine-mediated suppression of TGF-β1-driven fibroblast activation, supporting ASCs as a promising regenerative strategy for systemic sclerosis skin disease.

Indexed as

Adipose TissueAngiogenesisDermisScleroderma, SystemicStem CellsStem Cell TransplantationAnimalsBleomycinDisease Models, AnimalFibroblastsFibrosisInjections, IntralesionalMaleMiceMice, Inbred C57BLSkinBleomycinAdipose-derived stem cellsAngiogenesisFibrosisLaser doppler perfusion imagingSystemic sclerosis

Identifiers

PMID42033568
PMCPMC13212885

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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.