Evidence map›Paper›PMID 30168730›Full record

ArticleAmerican journal of physiology. Heart and circulatory physiology2018

Notch signaling regulates arterial vasoreactivity through opposing functions of Jagged1 and Dll4 in the vessel wall.

Sanchita Basu, Iulia Barbur, Alexander Calderon, Suhanti Banerjee, Aaron Proweller

Open access · bronzeAbstract read
In one paragraph

Article in American journal of physiology. Heart and circulatory physiology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.7field-weighted citation impact, top 27% 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

10 citing papers in PubMed, 14 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Progress to Clarify HowBiomolecules · 2024
    Review
  6. Notch Signaling in Acute Inflammation and Sepsis.International journal of molecular sciences · 2023
    Review
  7. Article
  8. Article
  9. Article
  10. "Yin and Yang" for Notch signaling in the mature vasculature.American journal of physiology. Heart and circulatory physiology · 2018
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors at 1 institution in 1 country.

Sanchita BasuDepartment of Medicine, Case Cardiovascular Research Institute and University Hospitals Harrington Heart and Vascular Institute, Case Western Reserve University , Cleveland, Ohio.
Iulia BarburDepartment of Medicine, Case Cardiovascular Research Institute and University Hospitals Harrington Heart and Vascular Institute, Case Western Reserve University , Cleveland, Ohio.
Alexander CalderonDepartment of Medicine, Case Cardiovascular Research Institute and University Hospitals Harrington Heart and Vascular Institute, Case Western Reserve University , Cleveland, Ohio.
Suhanti BanerjeeDepartment of Medicine, Case Cardiovascular Research Institute and University Hospitals Harrington Heart and Vascular Institute, Case Western Reserve University , Cleveland, Ohio.
Aaron ProwellerDepartment of Medicine, Case Cardiovascular Research Institute and University Hospitals Harrington Heart and Vascular Institute, Case Western Reserve University , Cleveland, Ohio.
Case Western Reserve University · US

Funding

Mechanisms of hypoxia-induced angiogenic control by vascular smooth muscleR01HL128281 · NHLBI · CASE WESTERN RESERVE UNIVERSITY · PI PROWELLER, AARON, RAMIREZ-BERGERON, DIANA L · 2016 to 2019
$2.1M
Vascular Smooth Muscle Notch Signaling in Arterial Patterning and FunctionR01HL096603 · NHLBI · CASE WESTERN RESERVE UNIVERSITY · PI PROWELLER, AARON · 2009 to 2013
$1.9M
NHLBI NIH HHS R01 HL096603NHLBI NIH HHS R01 HL128281
6 · The paper itself

Abstract

Functional interactions between endothelial cells (ECs) and smooth muscle cells (SMCs) in the arterial wall are necessary for controlling vasoreactivity that underlies vascular resistance and tone. Key signaling pathways converge on the phosphorylation of myosin light chain (p-MLC), the molecular signature of force production in SMCs, through coordinating the relative activities of myosin light chain kinase (MLCK) and myosin phosphatase (MP). Notch signaling in the vessel wall serves critical roles in arterial formation and maturation and has been implicated in arterial vasoregulation. In this report, we hypothesized that Notch signaling through ligands Jagged1 (in SMCs) and delta-like protein-4 (Dll4; in ECs) regulates vasoreactivity via homotypic (SMC-SMC) and heterotypic (EC-SMC) cell interactions. Using ligand induction assays, we demonstrated that Jagged1 selectively induced smooth muscle MLCK gene expression and p-MLC content while inhibiting MP function (i.e., increased Ca

Indexed as

VasoconstrictionVasodilationAdaptor Proteins, Signal TransducingAnimalsArteriesCalcium-Binding ProteinsCells, CulturedEndothelium, VascularIntracellular Signaling Peptides and ProteinsJagged-1 ProteinMaleMembrane ProteinsMiceMice, Inbred C57BLMuscle, Smooth, VascularMyosin-Light-Chain KinaseAdaptor Proteins, Signal TransducingCalcium-Binding Proteinscardiac myosin light chain kinase, mouseDLL4 protein, mouseIntracellular Signaling Peptides and ProteinsJagged-1 ProteinMembrane ProteinsMyosin-Light-Chain KinaseMyosin-Light-Chain PhosphataseNitric OxidePpp1r12a protein, mouseReceptors, Notchdelta-like protein-4Jagged1Notch signalingsmooth musclevasoreactivity

Identifiers

PMID30168730
PMCPMC6336965
OpenAlexW2889087919

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.