Evidence map›Paper›PMID 38733496›Full record

ArticleAngiogenesis2024

Distinct roles of SOX9 in self-renewal of progenitors and mesenchymal transition of the endothelium.

Jilai Zhao, Laura Sormani, Sebastien Jacquelin, Haiming Li, Cassandra Styke, Chenhao Zhou, Jonathan Beesley, Linus Oon, Simranpreet Kaur, Seen-Ling Sim and 7 more

Abstract read
In one paragraph

Article in Angiogenesis, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
  2. Oxidized LDL Induces Pro-Inflammatory Transcriptomic and Epigenomic Responses in Human CD4FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2026
    Article
  3. 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

17 authors.

Jilai Zhao *Frazer Institute, The University of Queensland, Dermatology Research Centre, Experimental Dermatology Group, Brisbane, QLD, 4102, Australia.ORCID 0000-0002-2354-3230
Laura Sormani *Frazer Institute, The University of Queensland, Dermatology Research Centre, Experimental Dermatology Group, Brisbane, QLD, 4102, Australia.ORCID 0000-0002-0838-2088
Sebastien JacquelinMater Research, Translational Research Institute, Macrophage Biology Laboratory, Brisbane, QLD, 4102, Australia.ORCID 0000-0001-5087-3641
Haiming LiFrazer Institute, The University of Queensland, Dermatology Research Centre, Experimental Dermatology Group, Brisbane, QLD, 4102, Australia.ORCID 0000-0002-6991-8114
Cassandra StykeFrazer Institute, The University of Queensland, Dermatology Research Centre, Experimental Dermatology Group, Brisbane, QLD, 4102, Australia.ORCID 0000-0002-7911-7855
Chenhao ZhouFrazer Institute, The University of Queensland, Dermatology Research Centre, Experimental Dermatology Group, Brisbane, QLD, 4102, Australia.
Jonathan BeesleyCancer Research Program, QIMR Berghofer Medical Research Institute, Brisbane, QLD, 4006, Australia.ORCID 0000-0003-1942-325X
Linus OonFrazer Institute, The University of Queensland, Dermatology Research Centre, Experimental Dermatology Group, Brisbane, QLD, 4102, Australia.
Simranpreet KaurFrazer Institute, The University of Queensland, Dermatology Research Centre, Experimental Dermatology Group, Brisbane, QLD, 4102, Australia.
Seen-Ling SimFrazer Institute, The University of Queensland, Dermatology Research Centre, Experimental Dermatology Group, Brisbane, QLD, 4102, Australia.
Ho Yi WongFrazer Institute, The University of Queensland, Dermatology Research Centre, Experimental Dermatology Group, Brisbane, QLD, 4102, Australia.ORCID 0000-0002-1245-4056
James DightFrazer Institute, The University of Queensland, Dermatology Research Centre, Experimental Dermatology Group, Brisbane, QLD, 4102, Australia.ORCID 0000-0002-9415-2368
Ghazaleh HashemiFrazer Institute, The University of Queensland, Dermatology Research Centre, Experimental Dermatology Group, Brisbane, QLD, 4102, Australia.ORCID 0000-0002-1326-8992
Abbas ShafieeFrazer Institute, The University of Queensland, Dermatology Research Centre, Experimental Dermatology Group, Brisbane, QLD, 4102, Australia.ORCID 0000-0002-8885-9025
Edwige RoyFrazer Institute, The University of Queensland, Dermatology Research Centre, Experimental Dermatology Group, Brisbane, QLD, 4102, Australia.ORCID 0000-0003-1991-5844
Jatin PatelCentre for Ageing Research Program, Queensland University of Technology, Brisbane, QLD, 4102, Australia.ORCID 0000-0002-3511-0029
Kiarash KhosrotehraniFrazer Institute, The University of Queensland, Dermatology Research Centre, Experimental Dermatology Group, Brisbane, QLD, 4102, Australia. k.khosrotehrani@uq.edu.au.ORCID 0000-0002-6406-4076

Funding

Department of Defense PR190852
6 · The paper itself

Abstract

Regenerative capabilities of the endothelium rely on vessel-resident progenitors termed endothelial colony forming cells (ECFCs). This study aimed to investigate if these progenitors are impacted by conditions (i.e., obesity or atherosclerosis) characterized by increased serum levels of oxidized low-density lipoprotein (oxLDL), a known inducer of Endothelial-to-Mesenchymal Transition (EndMT). Our investigation focused on understanding the effects of EndMT on the self-renewal capabilities of progenitors and the associated molecular alterations. In the presence of oxLDL, ECFCs displayed classical features of EndMT, through reduced endothelial gene and protein expression, function as well as increased mesenchymal genes, contractility, and motility. Additionally, ECFCs displayed a dramatic loss in self-renewal capacity in the presence of oxLDL. RNA-sequencing analysis of ECFCs exposed to oxLDL validated gene expression changes suggesting EndMT and identified SOX9 as one of the highly differentially expressed genes. ATAC sequencing analysis identified SOX9 binding sites associated with regions of dynamic chromosome accessibility resulting from oxLDL exposure, further pointing to its importance. EndMT phenotype and gene expression changes induced by oxLDL in vitro or high fat diet (HFD) in vivo were reversed by the silencing of SOX9 in ECFCs or the endothelial-specific conditional knockout of Sox9 in murine models. Overall, our findings support that EndMT affects vessel-resident endothelial progenitor's self-renewal. SOX9 activation is an early transcriptional event that drives the mesenchymal transition of endothelial progenitor cells. The identification of the molecular network driving EndMT in vessel-resident endothelial progenitors presents a new avenue in understanding and preventing a range of condition where this process is involved.

Indexed as

Lipoproteins, LDLSOX9 Transcription FactorAnimalsAtherosclerosisCell Self RenewalEndothelial CellsEndothelial Progenitor CellsEpithelial-Mesenchymal TransitionHumansMaleMiceMice, Inbred C57BLLipoproteins, LDLoxidized low density lipoproteinSOX9 protein, humanSox9 protein, mouseSOX9 Transcription FactorEndothelial colony forming cells (ECFCs)Endothelial-to-mesenchymal transition (EndMT)High fat diet (HFD)Oxidized low-density lipoprotein (oxLDL)Sox9Vessel-resident endothelial progenitors

Identifiers

PMID38733496
PMCPMC11303482

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.