Evidence map›Paper›PMID 32366833›Full record

ArticleCell death & disease2020

Atypical chemokine receptor ACKR3/CXCR7 controls postnatal vasculogenesis and arterial specification by mesenchymal stem cells via Notch signaling.

Sung-Tai Wei, Yen-Chih Huang, Mei-Ling Hsieh, Yu-Jung Lin, Woei-Cherng Shyu, Hui-Chen Chen, Chia-Hung Hsieh

Open access · goldAbstract read
In one paragraph

Article in Cell death & disease, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.0field-weighted citation impact, top 25% of its field
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

16 citing papers in PubMed, 21 citations in OpenAlex.

  1. Persistent ZnAdvanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
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  16. Modulation of p75International journal of molecular sciences · 2021
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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

7 authors at 2 institutions in 1 country.

Sung-Tai Wei *Graduate Institute of Biomedical Sciences, China Medical University, Taichung, Taiwan.
Yen-Chih Huang *Graduate Institute of Biomedical Sciences, China Medical University, Taichung, Taiwan.
Mei-Ling HsiehGraduate Institute of Immunology, China Medical University, Taichung, Taiwan.
Yu-Jung LinGraduate Institute of Biomedical Sciences, China Medical University, Taichung, Taiwan.
Woei-Cherng ShyuGraduate Institute of Immunology, China Medical University, Taichung, Taiwan.
Hui-Chen ChenGraduate Institute of Biomedical Sciences, China Medical University, Taichung, Taiwan.
Chia-Hung HsiehGraduate Institute of Biomedical Sciences, China Medical University, Taichung, Taiwan. chhsiehcmu@mail.cmu.edu.tw.
China Medical University · TWChina Medical University Hospital · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mesenchymal stem cells (MSCs) are known to play a role in postnatal vasculogenesis and hold great promise for vascular regeneration. However, the mechanisms by which the endothelial differentiation and specification of MSCs remain unclear. We examined the potential role and molecular mechanisms of atypical chemokine receptor ACKR3/CXCR7 in MSC-mediated endothelial cell differentiation and specification. Here, we showed that vascular endothelial growth factor (VEGF) and platelet-derived growth factor (PDGF) activate CXCR7 expression on MSCs through PDGF receptors, PDGFRα and PDGFRβ-mediated phosphoinositide 3-kinase (PI3K)/Akt signaling. Genetic and pharmacologic blockage of CXCR7 on MSCs suppressed the VEGF or stromal cell-derived factor 1 (SDF)-1-induced the capacity for vasculogenesis in vitro and in vivo. Moreover, CXCR7 gain of function markedly promoted vasculogenesis by MSCs in vitro and in vivo and induced endothelial differentiation along the arterial endothelial cell lineage via upregulation of Notch signaling. However, blockade of Notch signaling inhibited CXCR7-induced vasculogensis by MSCs. These results indicate CXCR7 is a critical regulator of MSC-mediated postnatal vasculogenesis and arterial specification via Notch signaling.

Indexed as

Neovascularization, PhysiologicSignal TransductionAnimalsArteriesCell LineChemokine CXCL12HumansMaleMesenchymal Stem CellsMice, Inbred C57BLMuscle CellsPhosphatidylinositol 3-KinasesPlatelet-Derived Growth FactorReceptor, Platelet-Derived Growth Factor alphaReceptor, Platelet-Derived Growth Factor betaReceptors, CXCRACKR3 protein, humanChemokine CXCL12Phosphatidylinositol 3-KinasesPlatelet-Derived Growth FactorReceptor, Platelet-Derived Growth Factor alphaReceptor, Platelet-Derived Growth Factor betaReceptors, CXCRReceptors, NotchRNA, MessengerVascular Endothelial Growth Factor A

Identifiers

PMID32366833
PMCPMC7198625
OpenAlexW3023573036

What OpenQuestion holds

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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 OpenQuestion graph.