Eosinophils develop in distinct stages and are recruited to peripheral sites by alternatively activated macrophages
Abstract
Eosinophils are associated with allergic diseases and helminth infections. Development of these cells and recruitment to peripheral tissues are only partially understood. Distinct stages of eosinophil development in fetal liver, bone marrow, and blood could be identified using IL-4 reporter mice and mAb against FIRE, Siglec-F, and CCR3. Immature eosinophils were present in the fetal liver and could reconstitute the eosinophil compartment in irradiated recipient mice. In adult mice, eosinophil maturation proceeded from CCR3− to CCR3+ cells in the bone marrow and was accompanied with changes in the transcriptional profile. Eosinophils appeared as activated cells in lung, thymus, lymph nodes, and Peyer’s patches but remained in a resting state in bone marrow, blood, and spleen. Mixed bone marrow chimeras revealed that recruitment to lung and peritoneum was dependent on Stat6 expression in noneosinophils. Alternatively activated macrophages contributed substantially to tissue recruitment of eosinophils, providing a novel basis for development of therapeutic approaches to lower tissue eosinophilia.
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These cells were eosinophilic progenitors based on CFU assays, cytospins and flow cytometry.
“These were eosinophilic progenitors based on CFU assays, cytospins and flow cytometry (Extended Data Fig. 10a–h)30.”
From Single-cell analysis of mixed-lineage states leading to a binary cell fate choice (2016) · cites this paper as [30]
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Single-cell analysis of mixed-lineage states leading to a binary cell fate choice
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- Authors
- Voehringer, D., van Rooijen, N., & Locksley, R. M.
- Affiliations
- Howard Hughes Medical Institute (US)
- Department of Molecular Cell Biology, Faculty of Medicine, Vrije Universiteit , Amsterdam , the Netherlands
- Corresponding author
- Locksley, Richard M
- Venue
- Journal of Leukocyte Biology
- Publisher
- Oxford University Press (OUP)
- Published
- 2007-03-05
- Volume
- 81
- Issue
- 6
- Pages
- 1434-1444
- ISSN
- 0741-5400 (ISSN-L)
- 1938-3673
- OpenAlex
- W2149589945
- Cited by
- 173
- References
- 51
- Citations by year
- 2026: 12 · 2025: 6 · 2024: 3 · 2023: 2 · 2022: 2 · 2021: 10 · 2020: 9 · 2019: 4 · 2018: 8 · 2017: 8 · 2016: 9 · 2015: 13 · 2014: 10 · 2013: 14 · 2012: 13
- FWCI
- 7.98
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Journal of Leukocyte Biology (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Institutes of Health (AI30663)
- Howard Hughes Medical Institute
- Sandler Asthma Basic Research Center
- Emmy Noether Program of the Deutsche Forschungsgemeinschaft (Vo944/2)
- Topics
- Health Sciences › Medicine › Physiology › Asthma and respiratory diseases
- Life Sciences › Immunology and Microbiology › Immunology › IL-33, ST2, and ILC Pathways
- Health Sciences › Medicine › Rheumatology › Eosinophilic Disorders and Syndromes
- Keywords
- eosinophils, eosinophil development, eosinophil recruitment, M2 macrophages, CCR3, STAT6, IL-4, Siglec-F, fire, fetal liver, bone marrow, tissue eosinophilia, eosinophil maturation, mixed bone marrow chimeras, allergic diseases, helminthiasis
- MeSH terms
- Animals, Bone Marrow, Cell Differentiation, Cell Movement, Eosinophils, Fetus, Liver, Macrophage Activation, Macrophages, Mice, Inbred BALB C, Organ Specificity, Peritoneal Cavity, Interleukin-4, Receptors, Chemokine, STAT6 Transcription Factor, Mice, Receptors, CCR3
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