Evidence map›Paper›PMID 34301845›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2021

Macrophage-Derived MicroRNA-21 Drives Overwhelming Glycolytic and Inflammatory Response during Sepsis via Repression of the PGE

Paulo De Melo, Annie Rocio Pineros Alvarez, Xiang Ye, Amondrea Blackman, Jose Carlos Alves-Filho, Alexandra I Medeiros, Jeffrey Rathmell, Heather Pua, C Henrique Serezani

Open access · greenAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 1 pooled it
1.4field-weighted citation impact, top 19% 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

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

  1. Pooled it
  2. Establishment of a murine resident dermal macrophage cell line.bioRxiv : the preprint server for biology · 2026
    Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Diagnostic and prognostic values ofNon-coding RNA research · 2023
    Article
  10. Article
  11. MicroRNAs in Macrophages: Regulators of Activation and Function.Journal of immunology (Baltimore, Md. : 1950) · 2023
    Review
  12. Article
  13. Article
  14. Article
  15. Microvesicle-Derived miRNAs Regulate Proinflammatory Macrophage Activation in the Lung Following Ozone Exposure.Toxicological sciences : an official journal of the Society of Toxicology · 2022
    Article
  16. Review
  17. 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

9 authors at 3 institutions in 2 countries.

Paulo De MeloDivision of Infectious Diseases, Department of Medicine, Vanderbilt University Medical Center, Nashville, TN.
Annie Rocio Pineros AlvarezIndiana Biosciences Research Institute, Indianapolis, IN.ORCID 0000-0003-0135-7549
Xiang YeDepartment of Pathology, Microbiology, and Immunology, Vanderbilt University Medical Center, Nashville, TN.ORCID 0000-0002-8694-8710
Amondrea BlackmanDivision of Infectious Diseases, Department of Medicine, Vanderbilt University Medical Center, Nashville, TN.ORCID 0000-0003-0785-938X
Jose Carlos Alves-FilhoDepartment of Pharmacology, School of Medicine of Ribeirão Preto, University of São Paulo, São Paulo, Brazil.ORCID 0000-0002-9918-8714
Alexandra I MedeirosDepartment of Biological Sciences, School of Pharmaceutical Sciences, São Paulo State University, Araraquara, São Paulo, Brazil.ORCID 0000-0001-6048-3647
Jeffrey RathmellDepartment of Pathology, Microbiology, and Immunology, Vanderbilt University Medical Center, Nashville, TN.ORCID 0000-0002-4106-3396
Heather PuaDepartment of Pathology, Microbiology, and Immunology, Vanderbilt University Medical Center, Nashville, TN.
C Henrique SerezaniDivision of Infectious Diseases, Department of Medicine, Vanderbilt University Medical Center, Nashville, TN; h.serezan@vumc.org.ORCID 0000-0002-5363-415X
Vanderbilt University Medical Center · USUniversidade de São Paulo · BRIndiana Biosciences Research Institute · US

Funding

Tumor Immunology and Microenvironment Research ProgramP30CA068485 · NCI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI STACIE B DUSETZINA · 1995 to 2026
$172.8M
Translational Analysis CoreP30DK058404 · NIDDK · VANDERBILT UNIVERSITY MEDICAL CENTER · PI RICHARD M. PEEK · 2002 to 2026
$29.9M
Vanderbilt Diabetes Research CenterP30DK020593 · NIDDK · VANDERBILT UNIVERSITY MEDICAL CENTER · PI ALVIN C POWERS · 2012 to 2026
$29.3M
Exploiting metabolic vulnerabilities of CD4 T cell subsets to control inflammatory diseaseR01DK105550 · NIDDK · VANDERBILT UNIVERSITY MEDICAL CENTER · PI Jeffrey C Rathmell · 2015 to 2026
$4.7M
Phosphatase and tensin homolog PTEN actions in polymicrobial sepsisR01HL124159 · NHLBI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI SEREZANI, C. HENRIQUE · 2014 to 2022
$4.2M
Initiative for Maximizing Student Development (IMSD) at VanderbiltT32GM139800 · NIGMS · VANDERBILT UNIVERSITY · PI RHOADES (STERLING), JULIE A, SEREZANI, C. HENRIQUE · 2021 to 2025
$3.7M
Prostaglandin E2 Actions and Enhanced Susceptibility to Skin Infection in Diabetic MiceR01DK122147 · NIDDK · VANDERBILT UNIVERSITY MEDICAL CENTER · PI SEREZANI, C. HENRIQUE · 2020 to 2022
$1.7M
T cell metabolism as a determinant of differentiation in allergic asthmaR01HL108006 · NHLBI · VANDERBILT UNIVERSITY · PI RATHMELL, JEFFREY C. · 2011 to 2014
$1.5M
MicroRNA-23 Cluster Regulation of Helper T cell Differentiation and FunctionK08AI116949 · NIAID · VANDERBILT UNIVERSITY MEDICAL CENTER · PI PUA, HEATHER H · 2015 to 2019
$828k
XFe96 AnalyzerS10OD018015 · OD · VANDERBILT UNIVERSITY · PI LANNIGAN, DEBORAH · 2014 to 2014
$200k
NCI NIH HHS P30 CA068485NHLBI NIH HHS R01 HL108006NHLBI NIH HHS R01 HL124159NIAID NIH HHS K08 AI116949NIDDK NIH HHS P30 DK020593NIDDK NIH HHS P30 DK058404NIDDK NIH HHS R01 DK105550NIDDK NIH HHS R01 DK122147NIGMS NIH HHS T32 GM139800NIH HHS S10 OD018015
6 · The paper itself

Abstract

Myeloid cells are critical for systemic inflammation, microbial control, and organ damage during sepsis. MicroRNAs are small noncoding RNAs that can dictate the outcome of sepsis. The role of myeloid-based expression of microRNA-21 (miR-21) in sepsis is inconclusive. In this study, we show that sepsis enhanced miR-21 expression in both peritoneal macrophages and neutrophils from septic C57BL/6J mice, and the deletion of miR-21 locus in myeloid cells (miR-21

Indexed as

AnimalsCells, CulturedCellular ReprogrammingDinoprostoneGlycolysisHumansInflammationInterleukin-10Macrophages, PeritonealMiceMice, Inbred C57BLMice, KnockoutMicroRNAsNeutrophilsSepsisDinoprostoneInterleukin-10MicroRNAsMIRN21 microRNA, mouse

Identifiers

PMID34301845
PMCPMC8323968
OpenAlexW3184695310

What OpenQuestion holds

Textmetadata
LicenceTDM
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.