Evidence map›Paper›PMID 36692963›Full record

ArticleJCI insight2023

Origin, prospective identification, and function of circulating endothelial colony-forming cells in mice and humans.

Yang Lin, Kimihiko Banno, Chang-Hyun Gil, Jered Myslinski, Takashi Hato, William C Shelley, Hongyu Gao, Xiaoling Xuei, Yunlong Liu, David P Basile and 9 more

Abstract read
In one paragraph

Article in JCI insight, 2023. 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. Article
  2. Review
  3. Direct in vivo reprogramming to relieve tissue ischemia via induced vasculogenesis.Molecular therapy : the journal of the American Society of Gene Therapy · 2025
    Review
  4. Article
  5. Article
  6. Article
  7. Review
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  9. Article
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  11. Article
  12. Review
  13. Article
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  16. Article
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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

19 authors.

Yang LinDepartment of Pediatrics, Indiana University School of Medicine, Indianapolis, Indiana, USA.
Kimihiko BannoDepartment of Pediatrics, Indiana University School of Medicine, Indianapolis, Indiana, USA.
Chang-Hyun GilDepartment of Pediatrics, Indiana University School of Medicine, Indianapolis, Indiana, USA.
Jered MyslinskiDepartment of Medicine.
Takashi HatoDepartment of Medicine.
William C ShelleyDepartment of Pediatrics, Indiana University School of Medicine, Indianapolis, Indiana, USA.
Hongyu GaoDepartment of Medical and Molecular Genetics, and.
Xiaoling XueiDepartment of Medical and Molecular Genetics, and.
Yunlong LiuDepartment of Medical and Molecular Genetics, and.
David P BasileDepartment of Anatomy Cell Biology and Physiology, Indiana University School of Medicine, Indianapolis, Indiana, USA.
Momoko YoshimotoDepartment of Pediatrics, Indiana University School of Medicine, Indianapolis, Indiana, USA.
Nutan PrasainDepartment of Pediatrics, Indiana University School of Medicine, Indianapolis, Indiana, USA.
Stefan P TarnawskyDepartment of Pediatrics, Indiana University School of Medicine, Indianapolis, Indiana, USA.
Ralf H AdamsMax Planck Institute for Molecular Biomedicine, Muenster, Germany.
Katsuhiko NaruseDepartment of Obstetrics & Gynecology, Nara Medical University, Kashihara, Nara, Japan.
Junko YoshidaDepartment of Physiology II, Nara Medical University, Kashihara, Nara, Japan.
Michael P MurphyDepartment of Surgery.
Kyoji HorieDepartment of Physiology II, Nara Medical University, Kashihara, Nara, Japan.
Mervin C YoderDepartment of Pediatrics, Indiana University School of Medicine, Indianapolis, Indiana, USA.

Funding

NITRIC OXIDE IN THE PATHOGENESIS OF DIABETIC RETINOPATHYR01EY012601 · NEI · UNIVERSITY OF FLORIDA · PI Julia V Busik, Maria Bartolomeo Grant · 1998 to 2026
$9.6M
A Clinical and Histological Analysis of Mesenchymal Stem Cells in AmputationR01HL128827 · NHLBI · INDIANA UNIVERSITY INDIANAPOLIS · PI MURPHY, MICHAEL PATRICK · 2016 to 2019
$1.8M
HSC-Independent Mechanisms Underlying JMMLR21CA202296 · NCI · INDIANA UNIVERSITY INDIANAPOLIS · PI KAPUR, REUBEN, YODER, MERVIN C. · 2016 to 2017
$375k
NCI NIH HHS R21 CA202296NEI NIH HHS R01 EY012601NHLBI NIH HHS R01 HL128827
6 · The paper itself

Abstract

Most circulating endothelial cells are apoptotic, but rare circulating endothelial colony-forming cells (C-ECFCs), also known as blood outgrowth endothelial cells, with proliferative and vasculogenic activity can be cultured; however, the origin and naive function of these C-ECFCs remains obscure. Herein, detailed lineage tracing revealed murine C-ECFCs emerged in the early postnatal period, displayed high vasculogenic potential with enriched frequency of clonal proliferative cells compared with tissue-resident ECFCs, and were not committed to or derived from the BM hematopoietic system but from tissue-resident ECFCs. In humans, C-ECFCs were present in the CD34bright cord blood mononuclear subset, possessed proliferative potential and in vivo vasculogenic function in a naive or cultured state, and displayed a single cell transcriptome sharing some umbilical venous endothelial cell features, such as a higher protein C receptor and extracellular matrix gene expression. This study provides an advance for the field by identifying the origin, naive function, and antigens to prospectively isolate C-ECFCs for translational studies.

Indexed as

Endothelial CellsExtracellular MatrixAnimalsClone CellsEndothelial Protein C ReceptorHumansMiceProspective StudiesEndothelial Protein C ReceptorEndothelial cellsVascular Biology

Identifiers

PMID36692963
PMCPMC10077473

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.