Evidence map›Paper›PMID 39308190›Full record

ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2024

Spatiotemporal Analysis of Mesenchymal Stem Cells Fate Determination by Inflammatory Niche Following Soft Tissue Injury at a Single-Cell Level.

Chen Kan, Zhenya Tan, Haitao Wang, Wei Wang, Jiazhao Yang, Ya Zhang, Xiaoling Lu, Qirong Cheng, Lanyi Chai, Chao Peng and 9 more

Abstract read
In one paragraph

Article in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing 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

24 citing papers in PubMed.

  1. Review
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  7. Article
  8. Review
  9. The cellular basis of fibrotic tendon healing: now in higher definition.American journal of physiology. Cell physiology · 2026
    Review
  10. Article
  11. The Role of Phagocytic Cells in the Achilles Tendon.International journal of molecular sciences · 2026
    Review
  12. Review
  13. Article
  14. Review
  15. Article
  16. Article
  17. Review
  18. Article
  19. Deciphering the Regulatory Networks of the Migrasome-Associated Cell Subpopulation in Heterotopic Ossification via Multi-Omics Analysis.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2025
    Article
  20. 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

19 authors.

Chen KanDepartment of Pathophysiology, School of Basic Medical Sciences, Anhui Medical University, Hefei, 230032, China.
Zhenya TanDepartment of Pathophysiology, School of Basic Medical Sciences, Anhui Medical University, Hefei, 230032, China.
Haitao WangDepartment of Physiology and Biomedical Engineering, Mayo Clinic, Rochester, MN, 55905, USA.
Wei WangDepartment of Pathophysiology, School of Basic Medical Sciences, Anhui Medical University, Hefei, 230032, China.
Jiazhao YangDepartment of Orthopedics, The First Affiliated Hospital of USTC, Hefei, 230001, China.
Ya ZhangDepartment of Pathophysiology, School of Basic Medical Sciences, Anhui Medical University, Hefei, 230032, China.
Xiaoling LuDepartment of Pathophysiology, School of Basic Medical Sciences, Anhui Medical University, Hefei, 230032, China.
Qirong ChengDepartment of Pathophysiology, School of Basic Medical Sciences, Anhui Medical University, Hefei, 230032, China.
Lanyi ChaiDepartment of Pathophysiology, School of Basic Medical Sciences, Anhui Medical University, Hefei, 230032, China.
Chao PengDepartment of Pathophysiology, School of Basic Medical Sciences, Anhui Medical University, Hefei, 230032, China.
Jicheng ZhuDepartment of Pathophysiology, School of Basic Medical Sciences, Anhui Medical University, Hefei, 230032, China.
Chenghang ZhuDepartment of Pathophysiology, School of Basic Medical Sciences, Anhui Medical University, Hefei, 230032, China.
Hailin WangDepartment of Pathophysiology, School of Basic Medical Sciences, Anhui Medical University, Hefei, 230032, China.
Li ZhanDepartment of Pathophysiology, School of Basic Medical Sciences, Anhui Medical University, Hefei, 230032, China.
Keqiong LinDepartment of Pathophysiology, School of Basic Medical Sciences, Anhui Medical University, Hefei, 230032, China.
Yakun LiuDepartment of Pathophysiology, School of Basic Medical Sciences, Anhui Medical University, Hefei, 230032, China.
Lingqiang ZhangState Key Laboratory of Medical Proteomics, National Center for Protein Sciences (Beijing), Beijing Institute of Lifeomics, Beijing, 100850, China.
Haitao FanDepartment of Orthopedics, The First Affiliated Hospital of Ningbo University, Ningbo, 315010, China.
Hong ZhengDepartment of Pathophysiology, School of Basic Medical Sciences, Anhui Medical University, Hefei, 230032, China.ORCID 0000-0002-4048-6530

Funding

Chinese scholarship council Research Collaboration Project, Scientific Research Project 0107048202Chinese scholarship council Research Collaboration Project, Scientific Research Project 2019xkjT004Chinese scholarship council Research Collaboration Project, Scientific Research Project XJ2020019Chinese scholarship council Research Collaboration Project, Scientific Research Project YJS20210259Collaborative Innovation Project of Anhui Universities GXXT-2021-063Natural Science Foundation of China 81870085Natural Science Foundation of China 82102573Natural Science Foundation of China 82173004Postdoctoral Fellowship Program of CPSF GZC20240010
6 · The paper itself

Abstract

Heterotopic ossification (HO), often arising in response to traumatic challenges, results from the aberrant osteochondral differentiation of mesenchymal stem cells (MSCs). Nevertheless, the impact of trauma-induced inflammatory exposure on MSC fate determination remains ambiguous. In this study, the cellular diversity within inflammatory lesions is elucidated, comprising MSCs and several innate and adaptive immune cells. It is observed that quiescent MSCs transition into cycling MSCs, subsequently giving rise to chondrogenic (cMSC) and/or osteogenic (oMSC) lineages within the inflammatory microenvironment following muscle or tendon injuries, as revealed through single-cell RNA sequencing (scRNA-seq), spatial transcriptome and lineage tracing analysis. Moreover, these investigations demonstrate that neutrophils and natural killer (NK) cells enhance transition of quiescent MSCs into cycling MSCs, which is also controlled by M1 macrophages, a subpopulation of macrophages can also stimulate cMSC and oMSC production from cycling MSCs. Additionally, M2 macrophages, CD4

Indexed as

Cell DifferentiationChondrogenesisInflammationMesenchymal Stem CellsAnimalsDisease Models, AnimalMiceMice, Inbred C57BLOsteogenesisSingle-Cell AnalysisSpatio-Temporal Analysisheterotopic ossificationinflammatory microenvironmentmesenchymal stem cellsosteoimmunology

Identifiers

PMID39308190
PMCPMC11578311

What Socratic holds

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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.