Evidence map›Paper›PMID 30355788›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2018

Circulating Plasma Extracellular Vesicles from Septic Mice Induce Inflammation via MicroRNA- and TLR7-Dependent Mechanisms.

Jinjin Xu, Yan Feng, Anjana Jeyaram, Steven M Jay, Lin Zou, Wei Chao

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 95 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
95citing papers in PubMed, 2 pooled it
4.4field-weighted citation impact, top 4% 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

95 citing papers in PubMed, 2 syntheses or guidelines pooled it, 126 citations in OpenAlex.

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  18. miR-574-5p in epigenetic regulation and Toll-like receptor signaling.Cell communication and signaling : CCS · 2024
    Review
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  20. Article

35 more citing papers are in PubMed but not listed here.

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.

Jinjin XuTranslational Research Program, Department of Anesthesiology and Center for Shock Trauma Anesthesiology Research, University of Maryland School of Medicine, Baltimore, MD 21201.ORCID 0000-0001-6154-9521
Yan FengTranslational Research Program, Department of Anesthesiology and Center for Shock Trauma Anesthesiology Research, University of Maryland School of Medicine, Baltimore, MD 21201.
Anjana JeyaramFischell Department of Bioengineering, University of Maryland, College Park, MD 20742.ORCID 0000-0002-2181-4367
Steven M JayFischell Department of Bioengineering, University of Maryland, College Park, MD 20742.ORCID 0000-0002-3827-5988
Lin ZouTranslational Research Program, Department of Anesthesiology and Center for Shock Trauma Anesthesiology Research, University of Maryland School of Medicine, Baltimore, MD 21201; wchao@som.umaryland.edu lzou@som.umaryland.edu.
Wei ChaoTranslational Research Program, Department of Anesthesiology and Center for Shock Trauma Anesthesiology Research, University of Maryland School of Medicine, Baltimore, MD 21201; wchao@som.umaryland.edu lzou@som.umaryland.edu.ORCID 0000-0002-2505-1360
University of Maryland, Baltimore · USUniversity of Maryland, College Park · US

Funding

Function and mechanisms of extracellular microRNAs in sepsis-induced lung injuryR35GM124775 · NIGMS · UNIVERSITY OF MARYLAND BALTIMORE · PI Lin Zou · 2017 to 2026
$3.2M
Role of TLR-cfB Signaling in SepsisR01GM097259 · NIGMS · UNIVERSITY OF MARYLAND BALTIMORE · PI CHAO, WEI · 2012 to 2015
$1.9M
Role of Extracellular MicroRNAs in Myocardial Ischemia-Reperfusion InjuryR01GM117233 · NIGMS · UNIVERSITY OF MARYLAND BALTIMORE · PI CHAO, WEI · 2016 to 2020
$1.6M
Extracellular miRNA-TLR7 Signaling in Sepsis PathogenesisR01GM122908 · NIGMS · UNIVERSITY OF MARYLAND BALTIMORE · PI CHAO, WEI · 2018 to 2019
$618k
NIGMS NIH HHS R01 GM097259NIGMS NIH HHS R01 GM117233NIGMS NIH HHS R01 GM122908NIGMS NIH HHS R35 GM124775
6 · The paper itself

Abstract

We have previously reported that a group of host cellular microRNAs (miRNAs; miR-34a-5p, miR-122-5p, miR-145-5p, miR-146a-5p, miR-210-3p) are released into the blood during sepsis, some of which are capable of inducing complement activation, cytokine production, and leukocyte migration. Extracellular vesicles (EVs) have been proposed as vehicles for extracellular miRNA-mediated intercellular communication. However, the biological function of plasma EVs and the associated miRNAs in sepsis are largely unknown. In this study, we tested the hypothesis that plasma EVs in sepsis are proinflammatory and EV-associated miRNAs are responsible for EV-induced cytokine production. Compared with those of sham mice, the plasma EVs from septic mice were slightly smaller (157 ± 2 versus 191 ± 6 nm,

Indexed as

AnimalsBlood CirculationCells, CulturedCytokinesDisease Models, AnimalExtracellular VesiclesHumansInflammationMacrophagesMembrane GlycoproteinsMiceMicroRNAsMyeloid Differentiation Factor 88PlasmaPolymyxin BSepsisCytokinesMembrane GlycoproteinsMicroRNAsMyeloid Differentiation Factor 88Polymyxin BTLR3 protein, mouseTlr7 protein, mouseToll-Like Receptor 3Toll-Like Receptor 7

Identifiers

PMID30355788
PMCPMC6240609
OpenAlexW2898551860

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.