Evidence map›Paper›PMID 36634143›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2023

Upregulation of Robo4 expression by SMAD signaling suppresses vascular permeability and mortality in endotoxemia and COVID-19 models.

Maaya Morita, Aki Yoneda, Nagisa Tokunoh, Tatsumi Masaki, Keisuke Shirakura, Mayumi Kinoshita, Rina Hashimoto, Naoya Shigesada, Junya Takahashi, Masashi Tachibana and 15 more

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
3.4field-weighted citation impact, top 8% 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

12 citing papers in PubMed, 22 citations in OpenAlex.

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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

25 authors at 6 institutions in 1 country.

Maaya MoritaGraduate School of Pharmaceutical Sciences, Osaka University, Osaka 565-0871, Japan.
Aki YonedaGraduate School of Pharmaceutical Sciences, Osaka University, Osaka 565-0871, Japan.
Nagisa TokunohResearch Institute for Microbial Diseases, Osaka University, Osaka 565-0871, Japan.
Tatsumi MasakiGraduate School of Pharmaceutical Sciences, Osaka University, Osaka 565-0871, Japan.
Keisuke ShirakuraGraduate School of Pharmaceutical Sciences, Osaka University, Osaka 565-0871, Japan.ORCID 0000-0002-9487-9495
Mayumi KinoshitaGraduate School of Pharmaceutical Sciences, Osaka University, Osaka 565-0871, Japan.
Rina HashimotoCenter for iPS Cell Research and Application, Kyoto University, Kyoto 606-8507, Japan.ORCID 0000-0002-7174-4563
Naoya ShigesadaGraduate School of Pharmaceutical Sciences, Osaka University, Osaka 565-0871, Japan.
Junya TakahashiGraduate School of Pharmaceutical Sciences, Osaka University, Osaka 565-0871, Japan.
Masashi TachibanaGraduate School of Pharmaceutical Sciences, Osaka University, Osaka 565-0871, Japan.ORCID 0000-0002-0376-508X
Shota TanakaGraduate School of Pharmaceutical Sciences, Osaka University, Osaka 565-0871, Japan.
Masanori ObanaGraduate School of Pharmaceutical Sciences, Osaka University, Osaka 565-0871, Japan.
Nobumasa HinoGraduate School of Pharmaceutical Sciences, Osaka University, Osaka 565-0871, Japan.
Masahito IkawaGraduate School of Pharmaceutical Sciences, Osaka University, Osaka 565-0871, Japan.ORCID 0000-0001-9859-6217
Kazutake TsujikawaGraduate School of Pharmaceutical Sciences, Osaka University, Osaka 565-0871, Japan.
Chikako OnoResearch Institute for Microbial Diseases, Osaka University, Osaka 565-0871, Japan.
Yoshiharu MatsuuraResearch Institute for Microbial Diseases, Osaka University, Osaka 565-0871, Japan.
Hiroyasu KidoyaDepartment of Integrative Vascular Biology, Faculty of Medical Sciences, University of Fukui, Fukui 910-1193, Japan.
Nobuyuki TakakuraResearch Institute for Microbial Diseases, Osaka University, Osaka 565-0871, Japan.
Yoshiaki KubotaDepartment of Anatomy, Keio University School of Medicine, Tokyo 160-8582, Japan.ORCID 0000-0001-6672-4122
Takefumi DoiGraduate School of Pharmaceutical Sciences, Osaka University, Osaka 565-0871, Japan.
Kazuo TakayamaCenter for iPS Cell Research and Application, Kyoto University, Kyoto 606-8507, Japan.ORCID 0000-0002-1132-2457
Yasuo YoshiokaGraduate School of Pharmaceutical Sciences, Osaka University, Osaka 565-0871, Japan.
Yasushi FujioGraduate School of Pharmaceutical Sciences, Osaka University, Osaka 565-0871, Japan.
Yoshiaki OkadaGraduate School of Pharmaceutical Sciences, Osaka University, Osaka 565-0871, Japan.ORCID 0000-0002-2962-244X
Osaka University of Pharmaceutical Sciences · JPOsaka International Cancer Institute · JPKyoto University · JPKeio University · JPThe University of Osaka · JPUniversity of Fukui · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

There is an urgent need to develop novel drugs to reduce the mortality from severe infectious diseases with the emergence of new pathogens, including Coronavirus disease 2019 (COVID-19). Although current drugs effectively suppress the proliferation of pathogens, immune cell activation, and inflammatory cytokine functions, they cannot completely reduce mortality from severe infections and sepsis. In this study, we focused on the endothelial cell-specific protein, Roundabout 4 (Robo4), which suppresses vascular permeability by stabilizing endothelial cells, and investigated whether enhanced Robo4 expression could be a novel therapeutic strategy against severe infectious diseases. Endothelial-specific overexpression of Robo4 suppresses vascular permeability and reduces mortality in lipopolysaccharide (LPS)-treated mice. Screening of small molecules that regulate Robo4 expression and subsequent analysis revealed that two competitive small mothers against decapentaplegic (SMAD) signaling pathways, activin receptor-like kinase 5 (ALK5)-SMAD2/3 and ALK1-SMAD1/5, positively and negatively regulate Robo4 expression, respectively. An ALK1 inhibitor was found to increase Robo4 expression in mouse lungs, suppress vascular permeability, prevent extravasation of melanoma cells, and decrease mortality in LPS-treated mice. The inhibitor suppressed severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2)-induced endothelial barrier disruption and decreased mortality in mice infected with SARS-CoV-2. These results indicate that enhancing Robo4 expression is an efficient strategy to suppress vascular permeability and mortality in severe infectious diseases, including COVID-19, and that small molecules that upregulate Robo4 can be potential therapeutic agents against these diseases.

Indexed as

COVID-19EndotoxemiaAnimalsCapillary PermeabilityEndothelial CellsLipopolysaccharidesMiceReceptors, Cell SurfaceSARS-CoV-2Signal TransductionUp-RegulationLipopolysaccharidesReceptors, Cell SurfaceRobo4 protein, mouseCOVID-19infectious diseaseRoundabout 4SMADvascular permeability

Identifiers

PMID36634143
PMCPMC9934020
OpenAlexW4315709061

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.