Evidence map›Paper›PMID 34431978›Full record

ArticleThe Journal of experimental medicine2021

Alveolar macrophages rely on GM-CSF from alveolar epithelial type 2 cells before and after birth.

Julia Gschwend, Samantha P M Sherman, Frederike Ridder, Xiaogang Feng, Hong-Erh Liang, Richard M Locksley, Burkhard Becher, Christoph Schneider

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of experimental medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 109 papers.

0numbers the graph read from it
0cells of the map it votes in
109citing papers in PubMed
8.6field-weighted citation impact, top 1% 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

109 citing papers in PubMed, 153 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Review
  5. Review
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Review
  13. Alveolar macrophage-neutrophil crosstalk in acute lung injury: mechanisms, feedback loops, and therapeutic opportunities.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2026
    Review
  14. Article
  15. Article
  16. Article
  17. Review
  18. Article
  19. Article
  20. Monocyte-Derived LGMNResearch (Washington, D.C.) · 2026
    Article

49 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 3 institutions in 2 countries.

Julia Gschwend *Institute of Physiology, University of Zurich, Zurich, Switzerland.ORCID 0000-0001-7212-4393
Samantha P M Sherman *Institute of Physiology, University of Zurich, Zurich, Switzerland.ORCID 0000-0002-0462-2005
Frederike RidderInstitute of Experimental Immunology, University of Zurich, Zurich, Switzerland.ORCID 0000-0002-3253-2322
Xiaogang FengInstitute of Physiology, University of Zurich, Zurich, Switzerland.ORCID 0000-0002-0343-1848
Hong-Erh LiangDepartment of Medicine, University of California San Francisco, San Francisco, CA.ORCID 0000-0003-0620-7224
Richard M LocksleyDepartment of Medicine, University of California San Francisco, San Francisco, CA.ORCID 0000-0002-5468-6867
Burkhard BecherInstitute of Experimental Immunology, University of Zurich, Zurich, Switzerland.ORCID 0000-0002-1541-7867
Christoph SchneiderInstitute of Physiology, University of Zurich, Zurich, Switzerland.ORCID 0000-0002-0452-2960
University of Zurich · CHHoward Hughes Medical Institute · USUniversity of California, San Francisco · US

Funding

Howard Hughes Medical InstituteNIH HHSSwiss National Science Foundation 310030_188450
6 · The paper itself

Abstract

Programs defining tissue-resident macrophage identity depend on local environmental cues. For alveolar macrophages (AMs), these signals are provided by immune and nonimmune cells and include GM-CSF (CSF2). However, evidence to functionally link components of this intercellular cross talk remains scarce. We thus developed new transgenic mice to profile pulmonary GM-CSF expression, which we detected in both immune cells, including group 2 innate lymphoid cells and γδ T cells, as well as AT2s. AMs were unaffected by constitutive deletion of hematopoietic Csf2 and basophil depletion. Instead, AT2 lineage-specific constitutive and inducible Csf2 deletion revealed the nonredundant function of AT2-derived GM-CSF in instructing AM fate, establishing the postnatal AM compartment, and maintaining AMs in adult lungs. This AT2-AM relationship begins during embryogenesis, where nascent AT2s timely induce GM-CSF expression to support the proliferation and differentiation of fetal monocytes contemporaneously seeding the tissue, and persists into adulthood, when epithelial GM-CSF remains restricted to AT2s.

Indexed as

AnimalsAnimals, NewbornCell DifferentiationCytokinesEpithelial CellsFemaleGene Expression Regulation, DevelopmentalGranulocyte-Macrophage Colony-Stimulating FactorImmunity, InnateLungMacrophages, AlveolarMiceMice, Inbred C57BLMice, KnockoutMice, TransgenicCytokinesGranulocyte-Macrophage Colony-Stimulating Factor

Identifiers

PMID34431978
PMCPMC8404471
OpenAlexW3195752138

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.