Evidence map›Paper›PMID 38703771›Full record

ArticleCell stem cell2024

Vascular architecture regulates mesenchymal stromal cell heterogeneity via P53-PDGF signaling in the mouse incisor.

Tingwei Guo, Fei Pei, Mingyi Zhang, Takahiko Yamada, Jifan Feng, Junjun Jing, Thach-Vu Ho, Yang Chai

Abstract read
In one paragraph

Article in Cell stem cell, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing 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

17 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. Targeting Arterial Dysfunction in Cardiovascular Disease Using Stem Cell-Based Therapies.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2026
    Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. Stem Cell Niche Concept: Search for Current Expert Consensus.International journal of molecular sciences · 2025
    Review
  10. Article
  11. Single-cell transcriptomics identifies PDGFRAInternational journal of oral science · 2025
    Article
  12. Article
  13. A spatially organizedScience advances · 2025
    Article
  14. Review
  15. Article
  16. Article
  17. 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

8 authors.

Tingwei GuoCenter for Craniofacial Molecular Biology, University of Southern California, Los Angeles, CA 90033, USA.
Fei PeiCenter for Craniofacial Molecular Biology, University of Southern California, Los Angeles, CA 90033, USA.
Mingyi ZhangCenter for Craniofacial Molecular Biology, University of Southern California, Los Angeles, CA 90033, USA.
Takahiko YamadaCenter for Craniofacial Molecular Biology, University of Southern California, Los Angeles, CA 90033, USA.
Jifan FengCenter for Craniofacial Molecular Biology, University of Southern California, Los Angeles, CA 90033, USA.
Junjun JingCenter for Craniofacial Molecular Biology, University of Southern California, Los Angeles, CA 90033, USA.
Thach-Vu HoCenter for Craniofacial Molecular Biology, University of Southern California, Los Angeles, CA 90033, USA.
Yang ChaiCenter for Craniofacial Molecular Biology, University of Southern California, Los Angeles, CA 90033, USA. Electronic address: ychai@usc.edu.

Funding

DOCTORAL AND POST-DOCTORAL TRAINING IN CRANIOFACIAL BIOLOGYT90DE021982 · NIDCR · UNIVERSITY OF SOUTHERN CALIFORNIA · PI PAINE, MICHAEL LANSDELL · 2011 to 2025
$6.2M
TGF BETA SIGNALING AND MANDIBULAR MORPHOGENESISR01DE012711 · NIDCR · UNIVERSITY OF SOUTHERN CALIFORNIA · PI CHAI, YANG · 1999 to 2023
$5.7M
TGF BETA SIGNALING AND CRANIOFACIAL MORPHOGENESISR37DE012711 · NIDCR · UNIVERSITY OF SOUTHERN CALIFORNIA · PI CHAI, YANG · 2009 to 2018
$4.3M
MOLECULAR REGULATORY MECHANISM OF MESENCHYMAL STEM CELLS IN ADULT MOUSE INCISORSR01DE025221 · NIDCR · UNIVERSITY OF SOUTHERN CALIFORNIA · PI Yang Chai · 2016 to 2026
$4.3M
NIDCR NIH HHS R01 DE012711NIDCR NIH HHS R01 DE025221NIDCR NIH HHS R37 DE012711NIDCR NIH HHS T90 DE021982
6 · The paper itself

Abstract

Mesenchymal stem cells (MSCs) reside in niches to maintain tissue homeostasis and contribute to repair and regeneration. Although the physiological functions of blood and lymphatic vasculature are well studied, their regulation of MSCs as niche components remains largely unknown. Using adult mouse incisors as a model, we uncover the role of Trp53 in regulating vascular composition through THBS2 to maintain mesenchymal tissue homeostasis. Loss of Trp53 in GLI1+ progeny increases arteries and decreases other vessel types. Platelet-derived growth factors from arteries deposit in the MSC region and interact with PDGFRA and PDGFRB. Significantly, PDGFRA+ and PDGFRB+ cells differentially contribute to defined cell lineages in the adult mouse incisor. Collectively, our results highlight Trp53's importance in regulating the vascular niche for MSCs. They also shed light on how different arterial cells provide unique cues to regulate MSC subpopulations and maintain their heterogeneity. Furthermore, they provide mechanistic insight into MSC-vasculature crosstalk.

Indexed as

IncisorMesenchymal Stem CellsSignal TransductionTumor Suppressor Protein p53AnimalsMicePlatelet-Derived Growth FactorReceptor, Platelet-Derived Growth Factor alphaReceptor, Platelet-Derived Growth Factor betaPlatelet-Derived Growth FactorReceptor, Platelet-Derived Growth Factor alphaReceptor, Platelet-Derived Growth Factor betaTrp53 protein, mouseTumor Suppressor Protein p53heterogeneity of MSCsPDGF signalingstem cell nicheTrp53vasculature

Identifiers

PMID38703771
PMCPMC11162319

What OpenQuestion 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 OpenQuestion graph.