Evidence map›Paper›PMID 12484607›Full record

ReviewTexas Heart Institute journal2002

Cellular precursors of the coronary arteries.

Ramón Muñoz-Chápuli, Mauricio González-Iriarte, Rita Carmona, Gerardo Atencia, David Macías, José María Pérez-Pomares

Open access · greenAbstract readReview
In one paragraph

Review in Texas Heart Institute journal, 2002. 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
1.0field-weighted citation impact, top 26% 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

17 citing papers in PubMed, 60 citations in OpenAlex.

  1. The Formation of Coronary Vessels in Cardiac Development and Disease.Cold Spring Harbor perspectives in biology · 2020
    Review
  2. Article
  3. Case report: a common trunk of the coronary arteries.Surgical and radiologic anatomy : SRA · 2017
    Article
  4. Article
  5. Review
  6. The clinical anatomy of the coronary arteries.Journal of cardiovascular translational research · 2013
    Review
  7. Article
  8. Article
  9. Article
  10. Expression of lymphatic markers during avian and mouse cardiogenesis.Anatomical record (Hoboken, N.J. : 2007) · 2010
    Article
  11. Article
  12. Coronary vessel development and insight towards neovascular therapy.International journal of experimental pathology · 2009
    Review
  13. Article
  14. Coronary endothelial proliferation and morphogenesis are regulated by a VEGF-mediated pathway.Developmental dynamics : an official publication of the American Association of Anatomists · 2009
    Article
  15. Review
  16. Review
  17. 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

6 authors at 1 institution in 1 country.

Ramón Muñoz-ChápuliDepartment of Animal Biology, Faculty of Science, University of Málaga, Málaga, Spain.
Mauricio González-Iriarte
Rita Carmona
Gerardo Atencia
David Macías
José María Pérez-Pomares
Universidad de Málaga · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Coronary vessels develop from a primary vascular network that differentiates in the subepicardium through a process of vasculogenesis, that is, self-assembly of mesenchymal vascular progenitors. Further growth of the subepicardial vascular plexus through a complex process of angiogenesis, vascular remodeling, and arterialization of specific branches gives rise to the definitive coronary system. This report is intended to summarize current knowledge on the origin of the coronary vascular progenitors and to provide new insights suggested by recent findings. It has been established that the mesenchymal precursors of the vascular smooth muscle cells and the adventitial fibroblasts originate from an epithelial-mesenchymal transformation of the epicardial mesothelium. We report herein experimental evidence that the precursors of the coronary endothelium are also epicardium-derived cells (EPDCs). The evidence shown includes co-localization of mesothelial and endothelial molecular markers as well as cell lineage studies performed through direct labeling of the epicardial cells. If this proposal is confirmed, the early EPDCs might be found to have a competence similar to that shown by the recently discovered bipotential vascular progenitor cells, which are able to differentiate into endothelium or smooth muscle depending on their exposure to VEGF or PDGF-BB. It is conceivable that the earliest EPDCs differentiate into endothelial cells in response to myocardially secreted VEGF, while subsequent EPDCs, recruited by the nascent capillaries via PDGFRbeta signaling, differentiate into percytes and smooth muscle cells.

Indexed as

Coronary Vessel AnomaliesEndothelium, VascularHumansMyocytes, Smooth Muscle

Identifiers

PMID12484607
PMCPMC140285
OpenAlexW1453493201

What OpenQuestion holds

Textmetadata
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.