Evidence map›Paper›PMID 30721157›Full record

ArticleJCI insight2019

Single cell RNA sequencing identifies unique inflammatory airspace macrophage subsets.

Kara J Mould, Nathan D Jackson, Peter M Henson, Max Seibold, William J Janssen

Abstract read
In one paragraph

Article in JCI insight, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 157 papers.

0numbers the graph read from it
0cells of the map it votes in
157citing papers in PubMed
–field-weighted citation impact
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

157 citing papers in PubMed.

  1. Myeloid cell reprogramming drives enhanced defense againstProceedings of the National Academy of Sciences of the United States of America · 2026
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97 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.

Kara J MouldDivision of Pulmonary, Critical Care and Sleep Medicine, Department of Medicine, National Jewish Health, Denver, Colorado, USA.
Nathan D JacksonCenter for Genes, Environment, and Health and.
Peter M HensonDivision of Pulmonary Sciences and Critical Care Medicine, Department of Medicine, University of Colorado - Anschutz Medical Campus, Aurora, Colorado, USA.
Max SeiboldDivision of Pulmonary Sciences and Critical Care Medicine, Department of Medicine, University of Colorado - Anschutz Medical Campus, Aurora, Colorado, USA.
William J JanssenDivision of Pulmonary, Critical Care and Sleep Medicine, Department of Medicine, National Jewish Health, Denver, Colorado, USA.

Funding

Lung Macrophage Programming in Acute Lung InjuryR35HL140039 · NHLBI · NATIONAL JEWISH HEALTH · PI JANSSEN, WILLIAM · 2018 to 2024
$6.4M
Mechanisms of lung macrophage programming by MUC5B during health and diseaseR01HL130938 · NHLBI · UNIVERSITY OF COLORADO DENVER · PI EVANS, CHRISTOPHER M · 2016 to 2025
$5.2M
Macrophage endocytosis in resolving lung inflammationR01HL114381 · NHLBI · NATIONAL JEWISH HEALTH · PI HENSON, PETER M · 2013 to 2016
$2.6M
Metabolic Reprogramming of Recruited Alveolar Macrophages by Arginine In Acute Lung InjuryK08HL141648 · NHLBI · NATIONAL JEWISH HEALTH · PI MOULD, KARA J · 2018 to 2022
$798k
Metabolic Programming of Alveolar Macrophages During Lung RepairF32HL131397 · NHLBI · UNIVERSITY OF COLORADO DENVER · PI MOULD, KARA J · 2016 to 2016
$66k
NHLBI NIH HHS F32 HL131397NHLBI NIH HHS K08 HL141648NHLBI NIH HHS R01 HL114381NHLBI NIH HHS R01 HL130938NHLBI NIH HHS R35 HL140039
6 · The paper itself

Abstract

Macrophages are well recognized for their dual roles in orchestrating inflammatory responses and regulating tissue repair. In almost all acutely inflamed tissues, 2 main subclasses of macrophages coexist. These include embryonically derived resident tissue macrophages and BM-derived recruited macrophages. While it is clear that macrophage subsets categorized in this fashion display distinct transcriptional and functional profiles, whether all cells within these categories and in the same inflammatory microenvironment share similar functions or whether further specialization exists has not been determined. To investigate inflammatory macrophage heterogeneity on a more granular level, we induced acute lung inflammation in mice and performed single cell RNA sequencing of macrophages isolated from the airspaces during health, peak inflammation, and resolution of inflammation. In doing so, we confirm that cell origin is the major determinant of alveolar macrophage (AM) programing, and, to our knowledge, we describe 2 previously uncharacterized, transcriptionally distinct subdivisions of AMs based on proliferative capacity and inflammatory programing.

Indexed as

Sequence Analysis, RNAAnimalsArginaseGene Expression ProfilingGene Expression RegulationGene Regulatory NetworksInflammationLipopolysaccharide ReceptorsMacrophages, AlveolarMaleMembrane GlycoproteinsMiceMice, Inbred C57BLNitric Oxide Synthase Type IIPneumoniaReceptors, ImmunologicArg1 protein, mouseArginaseCd14 protein, mouseLipopolysaccharide ReceptorsMembrane GlycoproteinsMRC1 protein, mouseNitric Oxide Synthase Type IINos2 protein, mouseReceptors, ImmunologicImmunologyMacrophagesPulmonology

Identifiers

PMID30721157
PMCPMC6483508

What OpenQuestion holds

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Registered trials

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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.