Evidence map›Paper›PMID 35679261›Full record

ArticleAmerican journal of respiratory cell and molecular biology2022

TLR7 Mediates Acute Respiratory Distress Syndrome in Sepsis by Sensing Extracellular miR-146a.

Huang Huang, Jing Zhu, Lili Gu, Jiang Hu, Xiujing Feng, Weiliang Huang, Sheng Wang, Yang Yang, Ping Cui, Shao-Hsuan Lin and 10 more

Open access · greenAbstract read
In one paragraph

Article in American journal of respiratory cell and molecular biology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed, 1 pooled it
2.3field-weighted citation impact, top 11% 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

22 citing papers in PubMed, 1 synthesis or guideline pooled it, 27 citations in OpenAlex.

  1. Pooled it
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  19. Myeloid Extracellular Vesicles: New Players in Indirect Lung Injury.American journal of respiratory cell and molecular biology · 2023
    Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

20 authors at 3 institutions in 1 country.

Huang HuangCenter for Shock, Trauma, and Anesthesiology Research and.ORCID 0000-0002-7858-7855
Jing ZhuCenter for Shock, Trauma, and Anesthesiology Research and.
Lili GuCenter for Shock, Trauma, and Anesthesiology Research and.ORCID 0000-0003-4727-4036
Jiang HuCenter for Shock, Trauma, and Anesthesiology Research and.ORCID 0000-0001-5284-0421
Xiujing FengCenter for Shock, Trauma, and Anesthesiology Research and.ORCID 0000-0002-8887-3302
Weiliang HuangDepartment of Pharmaceutical Sciences, School of Pharmacy, University of Maryland, Baltimore, Maryland.ORCID 0000-0002-9608-2172
Sheng WangCenter for Shock, Trauma, and Anesthesiology Research and.ORCID 0000-0002-5625-403X
Yang YangCenter for Shock, Trauma, and Anesthesiology Research and.ORCID 0000-0002-4178-1259
Ping CuiCenter for Shock, Trauma, and Anesthesiology Research and.ORCID 0000-0002-1272-5661
Shao-Hsuan LinCenter for Shock, Trauma, and Anesthesiology Research and.
Andrew SuenCenter for Shock, Trauma, and Anesthesiology Research and.ORCID 0000-0002-4354-6498
Briana K ShimadaCenter for Shock, Trauma, and Anesthesiology Research and.ORCID 0000-0003-1521-6966
Brittney WilliamsCenter for Shock, Trauma, and Anesthesiology Research and.ORCID 0000-0001-5835-2365
Maureen A KaneDepartment of Pharmaceutical Sciences, School of Pharmacy, University of Maryland, Baltimore, Maryland.ORCID 0000-0002-5525-9170
Yunbo KeCenter for Shock, Trauma, and Anesthesiology Research and.ORCID 0000-0002-4151-9058
Chen-Ou ZhangDivision of Pulmonary and Critical Care Medicine, School of Medicine, and.
Anna A BirukovaDivision of Pulmonary and Critical Care Medicine, School of Medicine, and.ORCID 0000-0003-0535-7693
Konstantin G BirukovCenter for Shock, Trauma, and Anesthesiology Research and.ORCID 0000-0002-0303-5394
Wei ChaoCenter for Shock, Trauma, and Anesthesiology Research and.ORCID 0000-0002-2505-1360
Lin ZouCenter for Shock, Trauma, and Anesthesiology Research and.ORCID 0000-0003-0820-4246
International Trauma Anesthesia and Critical Care Society · USPulmonary and Critical Care Associates · USUniversity of Maryland, Baltimore · US

Funding

Control of Lung Permeability by Oxidized PhospholipidsR01HL076259 · NHLBI · UNIVERSITY OF MARYLAND BALTIMORE · PI BIRUKOV, KONSTANTIN · 2004 to 2023
$6.8M
Training in Cardiovascular Research at the University of HawaiiT32HL115505 · NHLBI · UNIVERSITY OF HAWAII AT MANOA · PI Michelle D Tallquist · 2012 to 2026
$3.8M
Function and mechanisms of extracellular microRNAs in sepsis-induced lung injuryR35GM124775 · NIGMS · UNIVERSITY OF MARYLAND BALTIMORE · PI Lin Zou · 2017 to 2026
$3.2M
Targeting brain inflammation and neurocognitive dysfunction in sepsisR01NS110567 · NINDS · UNIVERSITY OF MARYLAND BALTIMORE · PI CHAO, WEI, WU, JUNFANG · 2019 to 2024
$2.5M
Extracellular miRNAs, innate immunity, and critical illnessR35GM140822 · NIGMS · UNIVERSITY OF MARYLAND BALTIMORE · PI WEI CHAO · 2021 to 2026
$2.5M
Control of septic inflammation and lung microvascular endothelial barrier by cell junction signaling nexusR01HL152761 · NHLBI · UNIVERSITY OF MARYLAND BALTIMORE · PI BIRUKOVA, ANNA · 2021 to 2024
$2.2M
Mechanisms of microvascular endothelial cell injury caused by extracellular histonesR01HL155051 · NHLBI · UNIVERSITY OF MARYLAND BALTIMORE · PI BIRUKOVA, ANNA · 2021 to 2024
$1.8M
Role of Extracellular MicroRNAs in Myocardial Ischemia-Reperfusion InjuryR01GM117233 · NIGMS · UNIVERSITY OF MARYLAND BALTIMORE · PI CHAO, WEI · 2016 to 2020
$1.6M
Modulation of inflammation in aging lungR01HL146829 · NHLBI · UNIVERSITY OF MARYLAND BALTIMORE · PI BIRUKOV, KONSTANTIN · 2020 to 2023
$1.5M
Extracellular miRNA-TLR7 Signaling in Sepsis PathogenesisR01GM122908 · NIGMS · UNIVERSITY OF MARYLAND BALTIMORE · PI CHAO, WEI · 2018 to 2019
$618k
Advanced components for an existing spinning disk confocal in an established core imaging facilityS10OD026698 · OD · UNIVERSITY OF MARYLAND BALTIMORE · PI BLANPIED, THOMAS A · 2019 to 2019
$274k
NHLBI NIH HHS R01 HL076259NHLBI NIH HHS R01 HL146829NHLBI NIH HHS R01 HL152761NHLBI NIH HHS R01 HL155051NHLBI NIH HHS T32 HL115505NIGMS NIH HHS R01 GM117233NIGMS NIH HHS R01 GM122908NIGMS NIH HHS R35 GM124775NIGMS NIH HHS R35 GM140822NIH HHS S10 OD026698NINDS NIH HHS R01 NS110567
6 · The paper itself

Abstract

TLR7 (Toll-like receptor 7), the sensor for single-stranded RNA, contributes to systemic inflammation and mortality in murine polymicrobial sepsis. Recent studies show that extracellular miR-146a-5p serves as a TLR7 ligand and plays an important role in regulating host innate immunity. However, the role of miR-146a-5p and TLR7 signaling in pulmonary inflammation, endothelial activation, and sepsis-associated acute respiratory distress syndrome remains unclear. Here, we show that intratracheal administration of exogenous miR-146a-5p in mice evokes lung inflammation, activates endothelium, and increases endothelial permeability via TLR7-dependent mechanisms. TLR7 deficiency attenuates pulmonary barrier dysfunction and reduces lung inflammatory response in a murine sepsis model. Moreover, the impact of miR-146a-5p-TLR7 signaling on endothelial activation appears to be a secondary effect because TLR7 is undetectable in the human pulmonary artery and microvascular endothelial cells (ECs), which show no response to direct miR-146a-5p treatment

Indexed as

Membrane GlycoproteinsMicroRNAsRespiratory Distress SyndromeSepsisToll-Like Receptor 7AnimalsCulture Media, ConditionedEndothelial CellsHumansMiceCulture Media, ConditionedMembrane GlycoproteinsMicroRNAsMirn146 microRNA, mouseTlr7 protein, mouseToll-Like Receptor 7acute respiratory distress syndromeinnate immunitymicroRNAssepsisToll-like receptors

Identifiers

PMID35679261
PMCPMC9447138
OpenAlexW4281989792

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.