Evidence map›Paper›PMID 22844117›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2012

Resolution of experimental lung injury by monocyte-derived inducible nitric oxide synthase.

Franco R D'Alessio, Kenji Tsushima, Neil R Aggarwal, Jason R Mock, Yoshiki Eto, Brian T Garibaldi, Daniel C Files, Claudia R Avalos, Jackie V Rodriguez, Adam T Waickman and 6 more

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
5.4field-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

29 citing papers in PubMed, 46 citations in OpenAlex.

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  8. Journal of microbiology and biotechnology · 2020
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  17. In vivo compartmental analysis of leukocytes in mouse lungs.American journal of physiology. Lung cellular and molecular physiology · 2015
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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

16 authors at 2 institutions in 1 country.

Franco R D'AlessioDivision of Pulmonary and Critical Care Medicine, The Johns Hopkins University School of Medicine, Baltimore, MD 21224, USA. fdaless2@jhmi.edu
Kenji Tsushima
Neil R Aggarwal
Jason R Mock
Yoshiki Eto
Brian T Garibaldi
Daniel C Files
Claudia R Avalos
Jackie V Rodriguez
Adam T Waickman
Sekhar P Reddy
David B Pearse
Venkataramana K Sidhaye
Paul M Hassoun
Michael T Crow
Landon S King
Johns Hopkins University · USJohns Hopkins Medicine · US

Funding

MULTIDISCIPLINARY TRAINING PROGRAM IN LUNG DISEASEST32HL007534 · NHLBI · JOHNS HOPKINS UNIVERSITY · PI Nadia N Hansel, Larissa A. Shimoda · 1985 to 2026
$28.3M
CELLULAR &MOLECULAR MECH OF INFLAMMATORY REACTIONST32AI007247 · NIAID · JOHNS HOPKINS UNIVERSITY · PI Joel L Pomerantz · 1985 to 2026
$10.2M
Phenotype-Specific Immune Responses in the Systemic VasculitidesP30AR053503 · NIAMS · JOHNS HOPKINS UNIVERSITY · PI BINGHAM, CLIFTON O · 2006 to 2015
$6.4M
Determinants of Resolution in Acute Lung InjuryR01HL089346 · NHLBI · JOHNS HOPKINS UNIVERSITY · PI KING, LANDON S · 2008 to 2012
$2.0M
Resolution and repair of acute lung injury by macrophage-derived iNOSR00HL103973 · NHLBI · JOHNS HOPKINS UNIVERSITY · PI D'ALESSIO, FRANCO RAFAEL · 2012 to 2014
$713k
Resolution and repair of acute lung injury by macrophage-derived iNOSK99HL103973 · NHLBI · JOHNS HOPKINS UNIVERSITY · PI D'ALESSIO, FRANCO RAFAEL · 2010 to 2011
$273k
NHLBI NIH HHS HL089346NHLBI NIH HHS K99 HL103973NHLBI NIH HHS R00 HL103973NHLBI NIH HHS R01 HL089346NHLBI NIH HHS T32 HL007534NIAID NIH HHS T32 AI007247NIAMS NIH HHS P30 AR053503
6 · The paper itself

Abstract

Although early events in the pathogenesis of acute lung injury (ALI) have been defined, little is known about the mechanisms mediating resolution. To search for determinants of resolution, we exposed wild type (WT) mice to intratracheal LPS and assessed the response at intervals to day 10, when injury had resolved. Inducible NO synthase (iNOS) was significantly upregulated in the lung at day 4 after LPS. When iNOS-/- mice were exposed to intratracheal LPS, early lung injury was attenuated; however, recovery was markedly impaired compared with WT mice. iNOS-/- mice had increased mortality and sustained increases in markers of lung injury. Adoptive transfer of WT (iNOS+/+) bone marrow-derived monocytes or direct adenoviral gene delivery of iNOS into injured iNOS-/- mice restored resolution of ALI. Irradiated bone marrow chimeras confirmed the protective effects of myeloid-derived iNOS but not of epithelial iNOS. Alveolar macrophages exhibited sustained expression of cosignaling molecule CD86 in iNOS-/- mice compared with WT mice. Ab-mediated blockade of CD86 in iNOS-/- mice improved survival and enhanced resolution of lung inflammation. Our findings show that monocyte-derived iNOS plays a pivotal role in mediating resolution of ALI by modulating lung immune responses, thus facilitating clearance of alveolar inflammation and promoting lung repair.

Indexed as

Acute Lung InjuryAnimalsB7-2 AntigenCell LineCell Line, TransformedDisease Models, AnimalInflammation MediatorsMacrophages, PeritonealMaleMiceMice, CongenicMice, Inbred C57BLMice, KnockoutMonocytesNitric Oxide Synthase Type IIB7-2 AntigenCd86 protein, mouseInflammation MediatorsNitric Oxide Synthase Type IINos2 protein, mouse

Identifiers

PMID22844117
PMCPMC3424351
OpenAlexW1769305035

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.