Evidence map›Paper›PMID 41226328›Full record

ArticleInternational journal of molecular sciences2025

Activin B Regulates Fibroblasts to Promote Granulation Tissue Formation and Angiogenesis During Murine Skin-Wound Healing via the JNK/ERK Signaling Pathway.

Jinfu Xu, Xueer Wang, Shan Zhao, Xiaofeng Chen, Wei Wu, Yarui Zhang, Qimei Chen, Xunhong Xu, Xinyu Yang, Min Zhang and 1 more

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2025. 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. Review
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.

Jinfu XuDepartment of Histology and Embryology, School of Basic Medical Sciences, Southern Medical University, Guangzhou 510515, China.
Xueer WangDepartment of Histology and Embryology, School of Basic Medical Sciences, Southern Medical University, Guangzhou 510515, China.
Shan ZhaoDepartment of Histology and Embryology, School of Basic Medical Sciences, Southern Medical University, Guangzhou 510515, China.
Xiaofeng ChenDepartment of Histology and Embryology, School of Basic Medical Sciences, Southern Medical University, Guangzhou 510515, China.
Wei WuDepartment of Histology and Embryology, School of Basic Medical Sciences, Southern Medical University, Guangzhou 510515, China.
Yarui ZhangDepartment of Histology and Embryology, School of Basic Medical Sciences, Southern Medical University, Guangzhou 510515, China.
Qimei ChenDepartment of Histology and Embryology, School of Basic Medical Sciences, Southern Medical University, Guangzhou 510515, China.
Xunhong XuDepartment of Histology and Embryology, School of Basic Medical Sciences, Southern Medical University, Guangzhou 510515, China.
Xinyu YangDepartment of Histology and Embryology, School of Basic Medical Sciences, Southern Medical University, Guangzhou 510515, China.
Min ZhangDepartment of Histology and Embryology, School of Basic Medical Sciences, Southern Medical University, Guangzhou 510515, China.ORCID 0009-0009-9545-6759
Lin ZhangDepartment of Histology and Embryology, School of Basic Medical Sciences, Southern Medical University, Guangzhou 510515, China.

Funding

Guangdong Basic and Applied Basic Research Foundation 2019A1515011213National Natural Science Foundation of China 81402613National Natural Science Foundation of China 81703147National Natural Science Foundation of China 82073417
6 · The paper itself

Abstract

Fibroblasts determine repair quality during skin-wound healing. Our previous study found that Activin B promotes keratinocyte proliferation and migration, facilitating re-epithelialization. However, specific mechanisms governing fibroblast function during wound healing remain unclear. Here, we aimed to elucidate the mechanism by which Activin B regulates fibroblast activity during skin-wound healing. Using a murine skin-wound model, we performed hematoxylin-eosin, immunohistochemical, and Masson's trichrome staining to evaluate Activin B's effects on granulation tissue formation, angiogenesis, and collagen fiber synthesis. We assessed Activin B's effects on fibroblast proliferation, migration, and collagen protein synthesis and investigated signaling pathway mechanisms in vitro. Animal experiments showed that Activin B accelerated wound healing by promoting granulation tissue regeneration and angiogenesis without affecting collagen fibers and Type I collagen synthesis. In vitro experiments demonstrated that Activin B modulates fibroblast proliferation and migration by activating JNK and ERK signaling pathways. Activin B may enhance angiogenesis by stimulating fibroblasts to secrete vascular endothelial growth factor, which induces dermal microvascular endothelial cell proliferation, promoting angiogenesis. Thus, we elucidated the dual regulatory paradigm of Activin B in fibroblasts; Activin B drives proliferation and migration via JNK/ERK signaling but does not directly regulate collagen synthesis.

Indexed as

ActivinsFibroblastsGranulation TissueMAP Kinase Signaling SystemNeovascularization, PhysiologicSkinWound HealingAngiogenesisAnimalsCell MovementCell ProliferationCollagenMaleMiceactivin BActivinsCollagenActivin Bangiogenesisfibroblastgranulation tissue formationJNK/ERK signaling pathwayskin-wound healing

Identifiers

PMID41226328
PMCPMC12607779

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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.