Evidence map›Paper›PMID 26780829›Full record

ArticleeLife2016

Heart of glass anchors Rasip1 at endothelial cell-cell junctions to support vascular integrity.

Bart-Jan de Kreuk, Alexandre R Gingras, James Dr Knight, Jian J Liu, Anne-Claude Gingras, Mark H Ginsberg

Open access · goldAbstract read
In one paragraph

Article in eLife, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
3.0field-weighted citation impact, top 10% 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

32 citing papers in PubMed, 58 citations in OpenAlex.

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  7. A cell atlas of thoracic aortic perivascular adipose tissue: a focus on mechanotransducers.American journal of physiology. Heart and circulatory physiology · 2024
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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 2 institutions in 2 countries.

Bart-Jan de KreukDepartment of Medicine, University of California, San Diego, San Diego, United States.
Alexandre R GingrasDepartment of Medicine, University of California, San Diego, San Diego, United States.
James Dr KnightLunenfeld-Tanenbaum Research Institute, Mount Sinai Hospital, Toronto, Canada.
Jian J LiuDepartment of Medicine, University of California, San Diego, San Diego, United States.
Anne-Claude GingrasLunenfeld-Tanenbaum Research Institute, Mount Sinai Hospital, Toronto, Canada.
Mark H GinsbergDepartment of Medicine, University of California, San Diego, San Diego, United States.ORCID http://orcid.org/0000-0002-5685-5417
Mount Sinai Hospital · CAUniversity of California San Diego · US

Funding

The Interaction of TPO and Integrins in Hematopoiesis CellsP01HL078784 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI GINSBERG, MARK HOWARD · 2005 to 2019
$28.3M
Somatic mutation(s) and cellular changes in CCM pathogenesisP01NS092521 · NINDS · DUKE UNIVERSITY · PI MARCHUK, DOUGLAS A. · 2015 to 2024
$12.9M
KRIT1 and Vascular IntegrityR01HL106489 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI GINSBERG, MARK HOWARD · 2011 to 2017
$2.3M
Composition and Functions of the Integrin Activation ComplexR01HL117807 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI GINSBERG, MARK HOWARD · 2014 to 2017
$1.5M
NHLBI NIH HHS P01 HL078784NHLBI NIH HHS R01 HL106489NHLBI NIH HHS R01 HL117807NINDS NIH HHS P01 NS092521
6 · The paper itself

Abstract

Heart of Glass (HEG1), a transmembrane receptor, and Rasip1, an endothelial-specific Rap1-binding protein, are both essential for cardiovascular development. Here we performed a proteomic screen for novel HEG1 interactors and report that HEG1 binds directly to Rasip1. Rasip1 localizes to forming endothelial cell (EC) cell-cell junctions and silencing HEG1 prevents this localization. Conversely, mitochondria-targeted HEG1 relocalizes Rasip1 to mitochondria in cells. The Rasip1-binding site in HEG1 contains a 9 residue sequence, deletion of which abrogates HEG1's ability to recruit Rasip1. HEG1 binds to a central region of Rasip1 and deletion of this domain eliminates Rasip1's ability to bind HEG1, to translocate to EC junctions, to inhibit ROCK activity, and to maintain EC junctional integrity. These studies establish that the binding of HEG1 to Rasip1 mediates Rap1-dependent recruitment of Rasip1 to and stabilization of EC cell-cell junctions.

Indexed as

Cell LineEndothelial CellsHumansIntercellular JunctionsIntracellular Signaling Peptides and ProteinsMembrane ProteinsProtein BindingHEG1 protein, humanIntracellular Signaling Peptides and ProteinsMembrane ProteinsRASIP1 protein, humancell biologydevelopmental biologyendothelial cellsHeart of GlasshumanRap1Rasip1Rho Kinasestem cells

Identifiers

PMID26780829
PMCPMC4733052
OpenAlexW2262241890

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.