Evidence map›Paper›PMID 36120937›Full record

ArticleJournal of leukocyte biology2022

Advanced age is associated with changes in alveolar macrophages and their responses to the stress of traumatic injury.

Devin M Boe, Holly J Hulsebus, Kevin M Najarro, Juliet E Mullen, Hyunmin Kim, Aik Choon Tan, Rachel H McMahan, Elizabeth J Kovacs

Abstract read
In one paragraph

Article in Journal of leukocyte biology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing 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

15 citing papers in PubMed.

  1. Review
  2. Review
  3. Macrophages on demand: How tissue trauma shapes their role.European journal of trauma and emergency surgery : official publication of the European Trauma Society · 2026
    Review
  4. Single-Cell Insights Into Macrophage Subtypes in Pulmonary Infections.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Review
  5. Article
  6. Parenchymal and inflammatory responses to ozone exposure in the aging healthy and surfactant protein C mutant lung.American journal of physiology. Lung cellular and molecular physiology · 2025
    Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Review
  12. Reducing the excessive inflammation after burn injury in aged mice by maintaining a healthier intestinal microbiome.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2024
    Article
  13. The guardians of pulmonary harmony: alveolar macrophages orchestrating the symphony of lung inflammation and tissue homeostasis.European respiratory review : an official journal of the European Respiratory Society · 2024
    Review
  14. Review
  15. Aging and macrophages: Not standing the test of time?Journal of leukocyte biology · 2022
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors.

Devin M BoeDepartment of Surgery, University of Colorado Anschutz Medical Campus, Aurora, Colorado, USA.
Holly J HulsebusDepartment of Surgery, University of Colorado Anschutz Medical Campus, Aurora, Colorado, USA.
Kevin M NajarroDepartment of Surgery, University of Colorado Anschutz Medical Campus, Aurora, Colorado, USA.
Juliet E MullenDepartment of Surgery, University of Colorado Anschutz Medical Campus, Aurora, Colorado, USA.
Hyunmin KimDepartment of Biostatistics and Bioinformatics, University of Colorado Anschutz Medical Campus, Aurora, Colorado, USA.
Aik Choon TanDepartment of Biostatistics and Bioinformatics, University of Colorado Anschutz Medical Campus, Aurora, Colorado, USA.
Rachel H McMahanDepartment of Surgery, University of Colorado Anschutz Medical Campus, Aurora, Colorado, USA.
Elizabeth J KovacsDepartment of Surgery, University of Colorado Anschutz Medical Campus, Aurora, Colorado, USA.

Funding

University of Colorado Cancer Center Support Grant - Lung Cancer Patient-Derived Xenografts with Autologous Human Immune SystemsP30CA046934 · NCI · UNIVERSITY OF COLORADO DENVER · PI James V Degregori · 1988 to 2026
$117.0M
Aging, macrophage mediators, and burn trauma: SupplementR01AG018859 · NIA · UNIVERSITY OF COLORADO DENVER · PI KOVACS, ELIZABETH J. · 2001 to 2024
$7.6M
Alcohol and Burn Trauma: Multi-organ Inflammatory ResponsesR35GM131831 · NIGMS · UNIVERSITY OF COLORADO DENVER · PI ELIZABETH J. KOVACS · 2019 to 2026
$3.5M
Alcohol and Lung Immunity in the AgedR21AA026295 · NIAAA · UNIVERSITY OF COLORADO DENVER · PI KOVACS, ELIZABETH J. · 2018 to 2019
$408k
Ethanol effects on pulmonary innate immunity in a murine model of agingF31AA027687 · NIAAA · UNIVERSITY OF COLORADO DENVER · PI HULSEBUS, HOLLY J · 2019 to 2021
$101k
Multi-organ Inflammatory Responses after Burn TraumaI01BX004335 · VA · VA EASTERN COLORADO HEALTH CARE SYSTEM · PI KOVACS, ELIZABETH J. · 2019 to 2023
–
BLRD VA I01 BX004335NCI NIH HHS P30 CA046934NIAAA NIH HHS F31 AA027687NIAAA NIH HHS R21 AA026295NIA NIH HHS R01 AG018859NIGMS NIH HHS R35 GM131831
6 · The paper itself

Abstract

Alveolar macrophages (AMs) are tissue-resident cells of the lower airways that perform many homeostatic functions critical for pulmonary health and protection against pathogens. However, little is known about the factors that shape AMs during healthy aging. In these studies, we sought to characterize age-related changes in AM phenotype, function, and responses to a physiologic stressor, that is, distal injury. Age was associated with a wide range of changes in cell surface receptor and gene expression by AMs, reflecting a unique alternatively activated phenotype. AMs from aged mice also exhibited markers of cellular senescence along with down-regulation of genes involved in growth and cell cycle pathways relative to young controls. Furthermore, AMs from aged mice showed a stunted transcriptional response to distal injury compared with AMs from young mice. Many changes were found to involve glucocorticoid-regulated genes, and corticosteroid treatment of primary AMs ex vivo revealed diminished transcriptional responses in cells from aged animals. These results demonstrate that there is a complex age-dependent AM phenotype associated with dysregulated stress hormone signaling that may interfere with AM responses to physiologic stressors and could contribute to AM dysfunction and the decline of pulmonary immunity during healthy aging.

Indexed as

LungMacrophages, AlveolarAnimalsMiceSignal Transductionglucocorticoidsinflammationinjurylungssenescence

Identifiers

PMID36120937
PMCPMC10150914

What OpenQuestion holds

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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.