Evidence map›Paper›PMID 33980844›Full record

ArticleNature communications2021

Mitofusin-2 stabilizes adherens junctions and suppresses endothelial inflammation via modulation of β-catenin signaling.

Young-Mee Kim, Sarah Krantz, Ankit Jambusaria, Peter T Toth, Hyung-Geun Moon, Isuru Gunarathna, Gye Young Park, Jalees Rehman

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
2.6field-weighted citation impact, top 9% 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

20 citing papers in PubMed, 43 citations in OpenAlex.

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  20. Review
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

8 authors at 1 institution in 1 country.

Young-Mee KimDivision of Cardiology, Department of Medicine, University of Illinois at Chicago, Chicago, IL, USA. youngmee@uic.edu.ORCID 0000-0001-6616-2393
Sarah KrantzDivision of Cardiology, Department of Medicine, University of Illinois at Chicago, Chicago, IL, USA.
Ankit JambusariaDivision of Cardiology, Department of Medicine, University of Illinois at Chicago, Chicago, IL, USA.ORCID 0000-0003-3039-2300
Peter T TothDepartment of Pharmacology and Regenerative Medicine, University of Illinois at Chicago, Chicago, IL, USA.ORCID 0000-0003-2168-0124
Hyung-Geun MoonDivision of Pulmonary, Critical Care, Sleep and Allergy, Department of Medicine, University of Illinois at Chicago, Chicago, IL, USA.
Isuru GunarathnaDivision of Cardiology, Department of Medicine, University of Illinois at Chicago, Chicago, IL, USA.
Gye Young ParkDivision of Pulmonary, Critical Care, Sleep and Allergy, Department of Medicine, University of Illinois at Chicago, Chicago, IL, USA.
Jalees RehmanDivision of Cardiology, Department of Medicine, University of Illinois at Chicago, Chicago, IL, USA. jalees@uic.edu.ORCID 0000-0002-2787-9292
University of Illinois Chicago · US

Funding

Virology Research Program (Program 4)P30CA016086 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI David Darr · 1985 to 2026
$201.5M
TRPC6 Regulation of Lung Endothelial Barrier FunctionP01HL060678 · NHLBI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI MALIK, ASRAR B. · 2000 to 2020
$40.1M
TRAINING PROGRAM IN LUNG BIOLOGY AND PATHOBIOLOGYT32HL007829 · NHLBI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI DOLLY MEHTA · 1995 to 2026
$15.6M
Integration Free IPS Cells-Derived Progenitors for Cardiac RegenerationR01HL126516 · NHLBI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI REHMAN, JALEES · 2015 to 2019
$3.0M
Amplification Mechanisms of Lung Endothelial Inflammation During Acute Lung InjuryR01HL152515 · NHLBI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI REHMAN, JALEES · 2021 to 2024
$2.3M
Training Program in Personalized Cardiovascular Medicine (TPIPCVM)T32HL139439 · NHLBI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI DARBAR, DAWOOD · 2018 to 2022
$2.1M
Role of alternatively activated macrophages in allergic asthmaR01HL126852 · NHLBI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI PARK, GYE YOUNG · 2016 to 2020
$2.0M
Endothelial Instruction of Macrophage Fate in Inflammatory InjuryR01HL154538 · NHLBI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI REHMAN, JALEES · 2021 to 2021
$128k
NCI NIH HHS P30 CA016086NHLBI NIH HHS P01 HL060678NHLBI NIH HHS R01 HL126516NHLBI NIH HHS R01 HL126852NHLBI NIH HHS R01 HL152515NHLBI NIH HHS R01 HL154538NHLBI NIH HHS T32 HL007829NHLBI NIH HHS T32 HL139439
6 · The paper itself

Abstract

Endothelial barrier integrity is ensured by the stability of the adherens junction (AJ) complexes comprised of vascular endothelial (VE)-cadherin as well as accessory proteins such as β-catenin and p120-catenin. Disruption of the endothelial barrier due to disassembly of AJs results in tissue edema and the influx of inflammatory cells. Using three-dimensional structured illumination microscopy, we observe that the mitochondrial protein Mitofusin-2 (Mfn2) co-localizes at the plasma membrane with VE-cadherin and β-catenin in endothelial cells during homeostasis. Upon inflammatory stimulation, Mfn2 is sulfenylated, the Mfn2/β-catenin complex disassociates from the AJs and Mfn2 accumulates in the nucleus where Mfn2 negatively regulates the transcriptional activity of β-catenin. Endothelial-specific deletion of Mfn2 results in inflammatory activation, indicating an anti-inflammatory role of Mfn2 in vivo. Our results suggest that Mfn2 acts in a non-canonical manner to suppress the inflammatory response by stabilizing cell-cell adherens junctions and by binding to the transcriptional activator β-catenin.

Indexed as

Adherens JunctionsAnimalsAntigens, CDbeta CateninBlotting, WesternCadherin 5CadherinsCell LineCell MembraneFemaleGTP PhosphohydrolasesHumansImmunoprecipitationMaleMiceMice, Inbred C57BLAntigens, CDbeta CateninCadherin 5CadherinsGTP PhosphohydrolasesMFN2 protein, humanMitochondrial Proteins

Identifiers

PMID33980844
PMCPMC8115264
OpenAlexW3161593843

What OpenQuestion holds

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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.