Evidence map›Paper›PMID 32371953›Full record

ArticleNature communications2020

A single-cell transcriptomic landscape of primate arterial aging.

Weiqi Zhang, Shu Zhang, Pengze Yan, Jie Ren, Moshi Song, Jingyi Li, Jinghui Lei, Huize Pan, Si Wang, Xibo Ma and 10 more

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Nature communications, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 119 papers.

0numbers the graph read from it
0cells of the map it votes in
119citing papers in PubMed
8.4field-weighted citation impact, top 1% 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

119 citing papers in PubMed, 164 citations in OpenAlex.

  1. Review
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  16. Biomarkers of ageing of humans and non-human primates.Nature reviews. Molecular cell biology · 2025
    Review
  17. Review
  18. Article
  19. Article
  20. Article

59 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

20 authors at 5 institutions in 3 countries.

Weiqi Zhang *CAS Key Laboratory of Genomic and Precision Medicine, Beijing Institute of Genomics, Chinese Academy of Sciences, Beijing, 100101, China.ORCID http://orcid.org/0000-0002-8885-5104
Shu Zhang *College of Life Sciences, Peking University, Beijing, 100871, China.
Pengze Yan *University of Chinese Academy of Sciences, Beijing, 100049, China.
Jie Ren *Biomedical Institute for Pioneering Investigation via Convergence, Peking University, Beijing, 100871, China.
Moshi SongUniversity of Chinese Academy of Sciences, Beijing, 100049, China.
Jingyi LiNational Laboratory of Biomacromolecules, CAS Center for Excellence in Biomacromolecules, Institute of Biophysics, Chinese Academy of Sciences, Beijing, 100101, China.
Jinghui LeiBeijing Institute for Brain Disorders, Advanced Innovation Center for Human Brain Protection, and National Clinical Research Center for Geriatric Disorders, Xuanwu Hospital Capital Medical University, Beijing, China.
Huize PanNational Laboratory of Biomacromolecules, CAS Center for Excellence in Biomacromolecules, Institute of Biophysics, Chinese Academy of Sciences, Beijing, 100101, China.
Si WangUniversity of Chinese Academy of Sciences, Beijing, 100049, China.
Xibo MaUniversity of Chinese Academy of Sciences, Beijing, 100049, China.
Shuai MaNational Laboratory of Biomacromolecules, CAS Center for Excellence in Biomacromolecules, Institute of Biophysics, Chinese Academy of Sciences, Beijing, 100101, China.
Hongyu LiNational Laboratory of Biomacromolecules, CAS Center for Excellence in Biomacromolecules, Institute of Biophysics, Chinese Academy of Sciences, Beijing, 100101, China.
Fei SunNational Laboratory of Biomacromolecules, CAS Center for Excellence in Biomacromolecules, Institute of Biophysics, Chinese Academy of Sciences, Beijing, 100101, China.
Haifeng WanUniversity of Chinese Academy of Sciences, Beijing, 100049, China.
Wei LiUniversity of Chinese Academy of Sciences, Beijing, 100049, China.ORCID http://orcid.org/0000-0001-7864-404X
Piu ChanBeijing Institute for Brain Disorders, Advanced Innovation Center for Human Brain Protection, and National Clinical Research Center for Geriatric Disorders, Xuanwu Hospital Capital Medical University, Beijing, China.
Qi ZhouUniversity of Chinese Academy of Sciences, Beijing, 100049, China.
Guang-Hui LiuNational Laboratory of Biomacromolecules, CAS Center for Excellence in Biomacromolecules, Institute of Biophysics, Chinese Academy of Sciences, Beijing, 100101, China. ghliu@ioz.ac.cn.ORCID http://orcid.org/0000-0001-9289-8177
Fuchou TangCollege of Life Sciences, Peking University, Beijing, 100871, China. tangfuchou@pku.edu.cn.ORCID http://orcid.org/0000-0002-8625-7717
Jing QuUniversity of Chinese Academy of Sciences, Beijing, 100049, China. qujing@ioz.ac.cn.ORCID http://orcid.org/0000-0002-3988-5067
Chinese Academy of Sciences · CNCapital Medical University · CNPeking University · CNInstitute for Stem Cell Biology and Regenerative Medicine · INInstitute of Automation · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Our understanding of how aging affects the cellular and molecular components of the vasculature and contributes to cardiovascular diseases is still limited. Here we report a single-cell transcriptomic survey of aortas and coronary arteries in young and old cynomolgus monkeys. Our data define the molecular signatures of specialized arteries and identify eight markers discriminating aortic and coronary vasculatures. Gene network analyses characterize transcriptional landmarks that regulate vascular senility and position FOXO3A, a longevity-associated transcription factor, as a master regulator gene that is downregulated in six subtypes of monkey vascular cells during aging. Targeted inactivation of FOXO3A in human vascular endothelial cells recapitulates the major phenotypic defects observed in aged monkey arteries, verifying FOXO3A loss as a key driver for arterial endothelial aging. Our study provides a critical resource for understanding the principles underlying primate arterial aging and contributes important clues to future treatment of age-associated vascular disorders.

Indexed as

AgingAnimalsAortaCoronary VesselsEndothelial CellsEndothelium, VascularForkhead Box Protein O3Macaca fascicularisSingle-Cell AnalysisTranscriptomeForkhead Box Protein O3FOXO3 protein, human

Identifiers

PMID32371953
PMCPMC7200799
OpenAlexW3022882962

What OpenQuestion holds

Textmetadata
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.