Evidence map›Paper›PMID 41701654›Full record

ArticleJCI insight2026

Dll4 assembles the umbilical cord and placental vasculature.

Derek C Sung, Hana A Ahanger, Sweta Narayan, Jesse A Pace, Mei Chen, Jisheng Yang, Siqi Gao, T C S Keller, Jenna Bockman, Xiaowen Chen and 5 more

Abstract read
In one paragraph

Article in JCI insight, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

15 authors.

Derek C SungCardiovascular Institute, Department of Medicine, and.
Hana A AhangerCardiovascular Institute, Department of Medicine, and.
Sweta NarayanCardiovascular Institute, Department of Medicine, and.
Jesse A PaceCardiovascular Institute, Department of Medicine, and.
Mei ChenCardiovascular Institute, Department of Medicine, and.
Jisheng YangCardiovascular Institute, Department of Medicine, and.
Siqi GaoCardiovascular Institute, Department of Medicine, and.
T C S KellerCardiovascular Institute, Department of Medicine, and.
Jenna BockmanCardiovascular Institute, Department of Medicine, and.
Xiaowen ChenCardiovascular Institute, Department of Medicine, and.
Erica NguyenCardiovascular Institute, Department of Medicine, and.
Alan T TangCardiovascular Institute, Department of Medicine, and.
Patricia Mericko-IshizukaCardiovascular Institute, Department of Medicine, and.
Ivan MaillardDivision of Hematologic Malignancies, Department of Medicine & Human Oncology and Pathogenesis Program, Memorial Sloan Kettering Cancer Center, New York, New York, USA.
Mark L KahnCardiovascular Institute, Department of Medicine, and.

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI SELWYN M VICKERS · 1985 to 2026
$347.4M
NCI NIH HHS P30 CA008748
6 · The paper itself

Abstract

Proper development of the umbilical cord and placental vasculature is essential for embryonic development. While the allantois is known give rise to endothelial cells (ECs) within the placenta, whether the allantois gives rise to ECs in the umbilical cord is debated. Furthermore, a lack of genetic tools to study placental vascular development independent of the embryo proper has hindered robust investigation into the primary cause of vascular defects from early studies utilizing global KOs. In this study, we delineate the contribution of the allantois to the umbilical vessels and utilize a mouse genetic tool previously developed by our lab to revisit the role of Notch signaling during placental development. We show that the allantois has mosaic contribution to the umbilical endothelium with higher contributions closer to the placenta. Allantoic deletion of Dll4 disrupts umbilical cord and placental vascular formation with secondary defects in the heart. Lastly, we identify Unc5b downstream of Notch signaling that restricts EC migration while promoting chemokine signaling for vascular smooth muscle cell (vSMC) recruitment to arteries. These findings identify a genetic tool for investigating placental vascular development and give insights into the ontogeny and mechanisms of placental vascular and umbilical cord development.

Indexed as

Adaptor Proteins, Signal TransducingCalcium-Binding ProteinsPlacentaUmbilical CordAllantoisAnimalsCell MovementEndothelial CellsFemaleHumansMembrane ProteinsMiceMice, KnockoutNeovascularization, PhysiologicPlacentationPregnancyAdaptor Proteins, Signal TransducingCalcium-Binding ProteinsDLL4 protein, mouseMembrane ProteinsReceptors, NotchAngiogenesisDevelopmentEndothelial cellsReproductive biologyVascular biology

Identifiers

PMID41701654
PMCPMC13134719

What Socratic 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 Socratic graph.