Evidence map›Paper›PMID 15563692›Full record

ArticleAmerican journal of respiratory cell and molecular biology2005

Monocytes recruited to the lungs of mice during immune inflammation ingest apoptotic cells poorly.

Jeffrey H Jennings, Derek J Linderman, Bin Hu, Joanne Sonstein, Jeffrey L Curtis

Open access · greenAbstract read
In one paragraph

Article in American journal of respiratory cell and molecular biology, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
0.8field-weighted citation impact, top 28% 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

18 citing papers in PubMed, 34 citations in OpenAlex.

  1. Recent advances in TAM mechanisms in lung diseases.Journal of translational medicine · 2025
    Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. TAM receptor signaling in immune homeostasis.Annual review of immunology · 2015
    Review
  7. Article
  8. Advances in gene therapy technologies to treat retinitis pigmentosa.Clinical ophthalmology (Auckland, N.Z.) · 2014
    Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Article
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 1 institution in 1 country.

Jeffrey H JenningsDivision of Pulmonary and Critical Care Medicine, Department of Internal Medicine, University of Michigan Health System, Ann Arbor, MI 48105, USA.
Derek J Linderman
Bin Hu
Joanne Sonstein
Jeffrey L Curtis
Michigan Medicine · US

Funding

SURFACTANT PROTEINS AND RESPIRATORY DISTRESS SYNDROMER37HL034788 · NHLBI · PENNSYLVANIA STATE UNIV HERSHEY MED CTR · PI FLOROS, JOANNA · 1996 to 2005
$3.2M
PULMONARY LYMPHOCYTE APOPTOSIS AND CELL CYCLE ARRESTR01HL056309 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI CURTIS, JEFFREY LOUIS · 1996 to 2010
$2.5M
NHLBI NIH HHS R01 HL056309NHLBI NIH HHS R01 HL56309NHLBI NIH HHS R37 HL034788NHLBI NIH HHS R37 HL34788
6 · The paper itself

Abstract

Apoptotic cells must be cleared to resolve inflammation, but few resident alveolar macrophages (AMo) from normal lungs ingest apoptotic cells. We examined how Mo ingestion of apoptotic cells is altered during immune inflammation induced by intratracheal challenge of primed C57BL/6 mice using sheep red blood cells. Resident AMo were labeled in situ before challenge using intravenous PKH26 to distinguish them from recruited monocytes. Using flow cytometry, we identified phagocytosis of fluorescently-labeled apoptotic thymocytes by alveolar mononuclear phagocytes in vitro and in vivo, and measured surface molecule expression. Intratracheal challenge induced rapid recruitment of monocytes, peaking at Day 3 and decreasing thereafter, whereas numbers of resident AMo did not change significantly. At all times, the percentage of phagocytes ingesting apoptotic thymocytes in vitro was greater among resident AMo (28-45%) than among recruited monocytes (9-19%), but was low in both cell types relative to ingestion of immunoglobulin-opsonized targets. There was also a nonsignificant trend toward lower ingestion by monocytes in vivo. MerTK, a receptor tyrosine kinase crucial for apoptotic cell phagocytosis, was expressed by resident AMo, but not by recruited monocytes. Relative to resident AMo, monocytes recruited to the alveolus ingest apoptotic cells meagerly, possibly due to absence of MerTK expression.

Indexed as

AnimalsApoptosisCell Movementc-Mer Tyrosine KinaseErythrocytesGene Expression RegulationInflammationLungMacrophage ActivationMacrophages, AlveolarMiceMonocytesPhagocytosisProto-Oncogene ProteinsReceptor Protein-Tyrosine KinasesSheepc-Mer Tyrosine KinaseMertk protein, mouseProto-Oncogene ProteinsReceptor Protein-Tyrosine Kinases

Identifiers

PMID15563692
PMCPMC2267037
OpenAlexW2086281650

What OpenQuestion holds

Textmetadata
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.