Evidence map›Paper›PMID 37787089›Full record

ArticleDevelopment (Cambridge, England)2023

Endothelial cell SMAD6 balances Alk1 function to regulate adherens junctions and hepatic vascular development.

Molly R Kulikauskas, Morgan Oatley, Tianji Yu, Ziqing Liu, Lauren Matsumura, Elise Kidder, Dana Ruter, Victoria L Bautch

Open access · hybridAbstract read
In one paragraph

Article in Development (Cambridge, England), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.6field-weighted citation impact, top 29% 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

6 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Generation ofRegenerative therapy · 2024
    Review
  6. Link between mutations inWorld journal of gastrointestinal surgery · 2024
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 1 institution in 1 country.

Molly R KulikauskasCell Biology and Physiology Curriculum, The University of North Carolina, Chapel Hill, NC 27599, USA.ORCID 0000-0001-5186-9740
Morgan OatleyDepartment of Biology, The University of North Carolina, Chapel Hill, NC 27599, USA.
Tianji YuDepartment of Biology, The University of North Carolina, Chapel Hill, NC 27599, USA.
Ziqing LiuDepartment of Biology, The University of North Carolina, Chapel Hill, NC 27599, USA.
Lauren MatsumuraDepartment of Biology, The University of North Carolina, Chapel Hill, NC 27599, USA.
Elise KidderDepartment of Biology, The University of North Carolina, Chapel Hill, NC 27599, USA.
Dana RuterDepartment of Biology, The University of North Carolina, Chapel Hill, NC 27599, USA.
Victoria L BautchCell Biology and Physiology Curriculum, The University of North Carolina, Chapel Hill, NC 27599, USA.ORCID 0000-0003-2135-5153
University of North Carolina at Chapel Hill · US

Funding

Virology Research Program (Program 4)P30CA016086 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI Deborah F. Tate · 1985 to 2026
$201.5M
MOLECULAR AND CELLULAR CONTROL OF ANGIOGENESISR35HL139950 · NHLBI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI BAUTCH, VICTORIA L · 2018 to 2024
$6.4M
NCI NIH HHS P30 CA016086NHLBI NIH HHS R35 HL139950
6 · The paper itself

Abstract

BMP signaling is crucial to blood vessel formation and function, but how pathway components regulate vascular development is not well-understood. Here, we find that inhibitory SMAD6 functions in endothelial cells to negatively regulate ALK1-mediated responses, and it is required to prevent vessel dysmorphogenesis and hemorrhage in the embryonic liver vasculature. Reduced Alk1 gene dosage rescued embryonic hepatic hemorrhage and microvascular capillarization induced by Smad6 deletion in endothelial cells in vivo. At the cellular level, co-depletion of Smad6 and Alk1 rescued the destabilized junctions and impaired barrier function of endothelial cells depleted for SMAD6 alone. Mechanistically, blockade of actomyosin contractility or increased PI3K signaling rescued endothelial junction defects induced by SMAD6 loss. Thus, SMAD6 normally modulates ALK1 function in endothelial cells to regulate PI3K signaling and contractility, and SMAD6 loss increases signaling through ALK1 that disrupts endothelial cell junctions. ALK1 loss-of-function also disrupts vascular development and function, indicating that balanced ALK1 signaling is crucial for proper vascular development and identifying ALK1 as a 'Goldilocks' pathway in vascular biology that requires a certain signaling amplitude, regulated by SMAD6, to function properly.

Indexed as

Adherens JunctionsEndothelial CellsActivin Receptors, Type IIHemorrhageHumansLiverPhosphatidylinositol 3-KinasesSmad6 ProteinActivin Receptors, Type IIACVRL1 protein, humanPhosphatidylinositol 3-KinasesSmad6 ProteinSMAD6 protein, humanAdherens junctionsALK1/ACVRL1BMPContractilityEndothelial cellsLiver developmentLiver sinusoidPI3KSMAD6Vascular barrier

Identifiers

PMID37787089
PMCPMC10629679
OpenAlexW4387297021

What OpenQuestion 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 OpenQuestion graph.