Evidence map›Paper›PMID 32909945›Full record

ArticleeLife2020

Vascular dimorphism ensured by regulated proteoglycan dynamics favors rapid umbilical artery closure at birth.

Sumeda Nandadasa, Jason M Szafron, Vai Pathak, Sae-Il Murtada, Caroline M Kraft, Anna O'Donnell, Christian Norvik, Clare Hughes, Bruce Caterson, Miriam S Domowicz and 7 more

Open access · goldAbstract read
In one paragraph

Article in eLife, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.4field-weighted citation impact, top 19% 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

14 citing papers in PubMed, 22 citations in OpenAlex.

  1. Review
  2. Article
  3. Feto-placental blood vessel development.Development (Cambridge, England) · 2025
    Review
  4. Review
  5. Article
  6. The mouse allantois: new insights at the embryonic-extraembryonic interface.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2022
    Review
  7. Article
  8. Article
  9. Article
  10. The versican-hyaluronan complex provides an essential extracellular matrix niche for Flk1Matrix biology : journal of the International Society for Matrix Biology · 2021
    Article
  11. Article
  12. Aggrecan in Cardiovascular Development and Disease.The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society · 2020
    Review
  13. Article
  14. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

17 authors at 7 institutions in 3 countries.

Sumeda NandadasaDepartment of Biomedical Engineering, Cleveland Clinic Lerner Research Institute, Cleveland, United States.ORCID 0000-0002-4954-6376
Jason M SzafronDepartment of Biomedical Engineering, Yale University, New Haven, United States.ORCID 0000-0001-9476-5175
Vai PathakCase Comprehensive Cancer Center, Case Western Reserve University, Cleveland, United States.
Sae-Il MurtadaDepartment of Biomedical Engineering, Yale University, New Haven, United States.
Caroline M KraftDepartment of Biomedical Engineering, Cleveland Clinic Lerner Research Institute, Cleveland, United States.
Anna O'DonnellDepartment of Biomedical Engineering, Cleveland Clinic Lerner Research Institute, Cleveland, United States.
Christian NorvikDepartment of Experimental Medical Science and Wallenberg Center for Molecular Medicine, Lund University, Lund, Sweden.
Clare HughesThe Sir Martin Evans Building, School of Biosciences, Cardiff University, Cardiff, United Kingdom.ORCID 0000-0003-4726-5877
Bruce CatersonThe Sir Martin Evans Building, School of Biosciences, Cardiff University, Cardiff, United Kingdom.
Miriam S DomowiczDepartment of Pediatrics, University of Chicago, Chicago, United States.ORCID 0000-0001-7860-4427
Nancy B SchwartzDepartment of Pediatrics, University of Chicago, Chicago, United States.
Karin Tran-LundmarkDepartment of Experimental Medical Science and Wallenberg Center for Molecular Medicine, Lund University, Lund, Sweden.
Martina VeiglCase Comprehensive Cancer Center, Case Western Reserve University, Cleveland, United States.
David SedwickDepartment of Medicine, Case Western Reserve University, Cleveland, United States.
Elliot H PhilipsonDepartment of Biomedical Engineering, Cleveland Clinic Lerner Research Institute, Cleveland, United States.
Jay D HumphreyDepartment of Biomedical Engineering, Yale University, New Haven, United States.ORCID 0000-0003-1011-2025
Suneel S ApteDepartment of Biomedical Engineering, Cleveland Clinic Lerner Research Institute, Cleveland, United States.ORCID 0000-0001-8441-1226
Cleveland Clinic Lerner College of Medicine · USCase Western Reserve University · USYale University · USCardiff University · GBLund University · SEUniversity of Chicago · USCleveland Clinic · US

Funding

TUMOR METABOLISM PROGRAMP30CA043703 · NCI · CASE WESTERN RESERVE UNIVERSITY · PI Amar Desai · 1987 to 2026
$142.3M
VERSICAN PROTEOLYSIS AND REGULATION OF VASCULAR SMOOTH MUSCLEP01HL107147 · NHLBI · CLEVELAND CLINIC LERNER COM-CWRU · PI HASCALL, VINCENT CHARLES · 2011 to 2017
$16.1M
Proteoglycan dynamics in pathogenesis of thoracic aortic aneurysm and dissectionR56HL141130 · NHLBI · CLEVELAND CLINIC LERNER COM-CWRU · PI APTE, SUNEEL S · 2018 to 2018
$400k
NCI NIH HHS P30 CA043703NHLBI NIH HHS P01 HL107147NHLBI NIH HHS R56 HL141130NICHD NIH HHS HHSN267200800009CNIH HHS CA43703NIH HHS HL107147NIH HHS HL141130
6 · The paper itself

Abstract

The umbilical artery lumen closes rapidly at birth, preventing neonatal blood loss, whereas the umbilical vein remains patent longer. Here, analysis of umbilical cords from humans and other mammals identified differential arterial-venous proteoglycan dynamics as a determinant of these contrasting vascular responses. The umbilical artery, but not the vein, has an inner layer enriched in the hydrated proteoglycan aggrecan, external to which lie contraction-primed smooth muscle cells (SMC). At birth, SMC contraction drives inner layer buckling and centripetal displacement to occlude the arterial lumen, a mechanism revealed by biomechanical observations and confirmed by computational analyses. This vascular dimorphism arises from spatially regulated proteoglycan expression and breakdown. Mice lacking aggrecan or the metalloprotease ADAMTS1, which degrades proteoglycans, demonstrate their opposing roles in umbilical vascular dimorphism, including effects on SMC differentiation. Umbilical vessel dimorphism is conserved in mammals, suggesting that differential proteoglycan dynamics and inner layer buckling were positively selected during evolution.

Indexed as

Myocytes, Smooth MuscleUmbilical ArteriesADAMTS1 ProteinAggrecansAnimalsCell DifferentiationFemaleHumansMice, TransgenicParturitionPregnancyADAMTS1 ProteinAdamts1 protein, mouseAggrecansbirthcomputational biologydevelopmental biologyextracellular matrixhumanmouseproteoglycanssystems biologyumbilical cordvascular engineeringvascular smooth muscle

Identifiers

PMID32909945
PMCPMC7529456
OpenAlexW3085511446

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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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.