Evidence map›Paper›PMID 37066416›Full record

ArticlebioRxiv : the preprint server for biology2024

Single cell 'omic profiles of human aortic endothelial cells

Maria L Adelus, Jiacheng Ding, Binh T Tran, Austin C Conklin, Anna K Golebiewski, Lindsey K Stolze, Michael B Whalen, Darren A Cusanovich, Casey E Romanoski

Open access · greenAbstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2024. 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, 0 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 1 institution in 1 country.

Maria L AdelusThe Department of Cellular and Molecular Medicine, The University of Arizona, Tucson, AZ 85721, USA.
Jiacheng DingThe Department of Cellular and Molecular Medicine, The University of Arizona, Tucson, AZ 85721, USA.
Binh T TranThe Department of Cellular and Molecular Medicine, The University of Arizona, Tucson, AZ 85721, USA.
Austin C ConklinThe Department of Cellular and Molecular Medicine, The University of Arizona, Tucson, AZ 85721, USA.
Anna K GolebiewskiThe Department of Cellular and Molecular Medicine, The University of Arizona, Tucson, AZ 85721, USA.
Lindsey K StolzeThe Department of Cellular and Molecular Medicine, The University of Arizona, Tucson, AZ 85721, USA.
Michael B WhalenThe Department of Cellular and Molecular Medicine, The University of Arizona, Tucson, AZ 85721, USA.
Darren A CusanovichThe Department of Cellular and Molecular Medicine, The University of Arizona, Tucson, AZ 85721, USA.
Casey E RomanoskiThe Department of Cellular and Molecular Medicine, The University of Arizona, Tucson, AZ 85721, USA.ORCID 0000-0002-0149-225X
University of Arizona · US

Funding

PHYSIOLOGYT32HL007249 · NHLBI · UNIVERSITY OF ARIZONA · PI Brett A Colson, JOHN P KONHILAS · 1985 to 2026
$12.5M
Mechanisms of ERG in Endothelial ActivationR01HL147187 · NHLBI · UNIVERSITY OF ARIZONA · PI ROMANOSKI, CASEY E · 2019 to 2023
$1.9M
Beyond Pseudotime: Enhanced Single-cell Genomics Tools for Understanding the Temporal Dynamics of Development and DiseaseR35GM137896 · NIGMS · UNIVERSITY OF ARIZONA · PI CUSANOVICH, DARREN A · 2020 to 2024
$1.8M
Human endothelial cell heterogeneity and activation in atherosclerosisF30HL162469 · NHLBI · UNIVERSITY OF ARIZONA · PI ADELUS, MARIA · 2022 to 2023
$84k
NHLBI NIH HHS F30 HL162469NHLBI NIH HHS R01 HL147187NHLBI NIH HHS T32 HL007249NIGMS NIH HHS R35 GM137896
6 · The paper itself

Abstract

Objective: Endothelial cells (ECs), macrophages, and vascular smooth muscle cells (VSMCs) are major cell types in atherosclerosis progression, and heterogeneity in EC sub-phenotypes are becoming increasingly appreciated. Still, studies quantifying EC heterogeneity across whole transcriptomes and epigenomes in both Approach and Results: To create an Conclusion: Primary EC cultures contain markedly heterogeneous cell subtypes defined by their molecular profiles. Surprisingly, the perturbations used here, which have been reported by others to be involved in the pathogenesis of atherosclerosis as well as induce endothelial-to-mesenchymal transition (EndMT), only modestly shifted cells between subpopulations, suggesting relatively stable molecular phenotypes in culture. Identifying consistently heterogeneous EC subpopulations between

Identifiers

PMID37066416
PMCPMC10104082
OpenAlexW4362678448

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.