Evidence map›Paper›PMID 41596210›Full record

ReviewInternational journal of molecular sciences2026

Circulating Fibrocytes: Cellular Mediators of Tissue Fibrosis.

Xinya Guo, Jianyu Lu, Yiyao Du, Zhaofan Xia, Shizhao Ji

Abstract readReview
In one paragraph

Review in International journal of molecular sciences, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Xinya GuoDepartment of Burn Surgery, The First Affiliated Hospital of Naval Medical University, Shanghai 200433, China.ORCID 0009-0007-5080-5914
Jianyu LuDepartment of Burn Surgery, The First Affiliated Hospital of Naval Medical University, Shanghai 200433, China.ORCID 0009-0005-2908-5014
Yiyao DuDepartment of Burn Surgery, The First Affiliated Hospital of Naval Medical University, Shanghai 200433, China.ORCID 0009-0005-7444-4813
Zhaofan XiaDepartment of Burn Surgery, The First Affiliated Hospital of Naval Medical University, Shanghai 200433, China.ORCID 0000-0002-8192-2693
Shizhao JiDepartment of Burn Surgery, The First Affiliated Hospital of Naval Medical University, Shanghai 200433, China.ORCID 0000-0002-5083-288X

Funding

Excellent Academic Leader Project of Shanghai Science and Technology Committee 23XD1425000Key Research Center Construction Project of Shanghai 2023ZZ02013National Key R&D Program of China 2024YFA1108405National Natural Science Foundation of China 82472546Science and Technology Innovation Project of Shanghai Science and Technology Committee 25CL2900703Shanghai Top Priority Research Center Project 2023ZZ02013
6 · The paper itself

Abstract

Fibrosis is a pathological condition resulting from an excessive tissue response during the repair process, often affecting various tissues such as the skin, organs, and joints, posing a significant threat to global health. Researchers have made substantial efforts to explore the endogenous mechanisms underlying fibrosis in recent years and have developed several therapeutic strategies to block this process. Historically, research on fibrotic diseases has focused on identifying highly relevant therapeutic targets and developing effective antifibrotic drugs. However, due to the complexity of the mechanisms of fibrosis and its effector cells, the effectiveness of antifibrotic therapies remains limited. With the advancement of high-throughput omics technologies and machine learning tools, we now have a clearer understanding of cellular heterogeneity, intercellular interactions, and the specific roles of cells in various biological processes. This enables tracking the trajectory of different cell types during the fibrotic process, facilitating early identification and discovery of new targets for fibrosis treatment, and conducting more precise targeted research. Supported by these novel technologies, numerous studies have revealed that, in addition to normal fibroblasts, a group of bone marrow-derived fibrocytes also contributes to the fibrosis of both parenchymal and non-parenchymal organs and tissues. Circulating fibrocytes are hematopoietic-derived cells that are recruited to injury sites during injury, disease, and aging, acting as participants in inflammation and tissue repair, and directly or indirectly promoting fibrosis in various tissues throughout the body. This review summarizes the general characteristics of circulating fibrocytes, the molecular mechanisms involved in their recruitment to different tissues, the process of their differentiation into fibroblasts, their potential roles in various diseases, and the latest research developments in this field. Given the key role of circulating fibrocytes in fibrosis across multiple tissues, they may serve as promising targets for the development of novel antifibrotic therapies.

Indexed as

FibroblastsFibrosisAnimalsHumanscirculating fibrocytesfibrosis

Identifiers

PMID41596210
PMCPMC12840654

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.