Evidence map›Paper›PMID 28674181›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2017

Lung Epithelial Cell-Derived Microvesicles Regulate Macrophage Migration via MicroRNA-17/221-Induced Integrin β

Heedoo Lee, Duo Zhang, Jingxuan Wu, Leo E Otterbein, Yang Jin

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 70 papers.

0numbers the graph read from it
0cells of the map it votes in
70citing papers in PubMed
5.1field-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

70 citing papers in PubMed, 101 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Pilot study ofRespiratory research · 2025
    Article
  5. Review
  6. Article
  7. Article
  8. Harmonising cellular conversations: decoding the vital roles of extracellular vesicles in respiratory system intercellular communications.European respiratory review : an official journal of the European Respiratory Society · 2024
    Review
  9. Review
  10. Review
  11. Article
  12. Review
  13. Article
  14. Review
  15. Extracellular vesicle-encapsulated CC16 as novel nanotherapeutics for treatment of acute lung injury.Molecular therapy : the journal of the American Society of Gene Therapy · 2023
    Article
  16. Review
  17. Article
  18. Review
  19. Article
  20. Article

10 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

5 authors at 2 institutions in 1 country.

Heedoo LeeDivision of Pulmonary and Critical Care Medicine, Department of Medicine, Boston University, Boston, MA 02118; and.ORCID 0000-0002-2168-3643
Duo ZhangDivision of Pulmonary and Critical Care Medicine, Department of Medicine, Boston University, Boston, MA 02118; and.
Jingxuan WuDivision of Pulmonary and Critical Care Medicine, Department of Medicine, Boston University, Boston, MA 02118; and.ORCID 0000-0002-3128-7601
Leo E OtterbeinDepartment of Surgery, Harvard Medical School, Beth Israel Deaconess Medical Center, Boston, MA 02215.
Yang JinDivision of Pulmonary and Critical Care Medicine, Department of Medicine, Boston University, Boston, MA 02118; and yjin1@bu.edu.
Boston University · USBeth Israel Deaconess Medical Center · US

Funding

Cross talk between cav-1 and flot1 in lung injuryR01HL102076 · NHLBI · BRIGHAM AND WOMEN'S HOSPITAL · PI JIN, YANG · 2011 to 2015
$2.1M
Development of the RNA molecule-enriched, cell type-specific exosomesR33AI121644 · NIAID · BOSTON UNIVERSITY MEDICAL CAMPUS · PI JIN, YANG · 2018 to 2020
$1.4M
Mechanistic insights into the systemic inflammation and organ failure in sepsisR01GM111313 · NIGMS · BRIGHAM AND WOMEN'S HOSPITAL · PI JIN, YANG · 2014 to 2017
$1.3M
Development of the RNA molecule-enriched, cell type-specific exosomesR21AI121644 · NIAID · BOSTON UNIVERSITY MEDICAL CAMPUS · PI JIN, YANG · 2016 to 2017
$444k
NHLBI NIH HHS R01 HL102076NIAID NIH HHS R21 AI121644NIAID NIH HHS R33 AI121644NIGMS NIH HHS R01 GM111313
6 · The paper itself

Abstract

Robust lung inflammation is one of the prominent features in the pathogenesis of acute lung injury (ALI). Macrophage migration and recruitment are often seen at the early stage of lung inflammatory responses to noxious stimuli. Using an acid inhalation-induced lung injury model, we explored the mechanisms by which acid exposure initiates macrophage recruitment and migration during development of ALI. The lung epithelium comprises a large surface area and functions as a first-line defense against noxious insults. We found that acid exposure induced a remarkable microvesicle (MV) release from lung epithelium as detected in bronchoalveolar lavage fluid. Significantly elevated RNA, rather than protein, was found in these epithelium-derived MVs after acid and included several highly elevated microRNAs, including microRNA (miR)-17 and miR-221. Acid-induced epithelial MV release promoted macrophage migration in vitro and recruitment into the lung in vivo and required, in part, MV shuttling of miR-17 and/or miR-221. Mechanistically, acid-induced epithelial MV miR-17/221 promoted β

Indexed as

Cell-Derived MicroparticlesAcute Lung InjuryAnimalsBronchoalveolar Lavage FluidCell MovementDisease Models, AnimalEpithelial CellsHydrochloric AcidInflammationIntegrin beta1LungMacrophagesMiceMicroRNAsHydrochloric AcidIntegrin beta1MicroRNAsMirn17 microRNA, mouseMIRN221 microRNA, mouse

Identifiers

PMID28674181
PMCPMC5561736
OpenAlexW2731262794

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.