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Updated: May 18, 2026

Proliferation and Differentiation of Murine Myeloid Precursor 32D/G-CSF-R Cells
Published on: February 21, 2018
Colony stimulating factors and myeloid cell biology in health and disease
John A Hamilton1, Adrian Achuthan
1Arthritis and Inflammation Research Centre, University of Melbourne Department of Medicine, The Royal Melbourne Hospital, Parkville, VIC 3050, Australia. jahami@unimelb.edu.au
Insights
Colony stimulating factors (CSFs) regulate myeloid cells. New insights into CSF function, particularly the role of interleukin-34, are reshaping our understanding of their role in health and disease.
Area of Science:
- Immunology
- Hematology
- Cell Biology
Background:
- Colony stimulating factors (CSFs) like GM-CSF, M-CSF, and G-CSF are critical regulators of myeloid cell development and function.
- These factors play roles in both normal physiological conditions (steady state) and inflammatory responses.
- Preclinical studies indicate potential therapeutic benefits of targeting CSFs in autoimmune and inflammatory diseases.
Purpose of the Study:
- To review recent advancements in understanding CSF function.
- To discuss the impact of CSF and CSF receptor manipulation studies on myeloid cell biology.
- To highlight the emerging role of interleukin-34 (IL-34) in CSF biology.
Main Methods:
- Analysis of studies involving CSF or CSF receptor neutralization/deletion.
- Review of data from CSF administration experiments.
- Examination of findings from preclinical and clinical investigations.
Main Results:
- CSFs are confirmed regulators of myeloid cell numbers and functions in various conditions.
- CSF targeting strategies are under clinical investigation for inflammatory and autoimmune diseases.
- The identification of IL-34 as an M-CSF receptor ligand necessitates a re-evaluation of M-CSF signaling pathways.
Conclusions:
- CSF biology is complex, with ongoing debates regarding their precise roles in specific myeloid cell populations.
- Interleukin-34 significantly impacts the understanding of macrophage-CSF (M-CSF) function.
- Further research into CSF and IL-34 pathways is crucial for developing novel immunomodulatory therapies.
Abstract:
The colony stimulating factors (CSFs), granulocyte macrophage-CSF (GM-CSF), macrophage-CSF (M-CSF or CSF-1) and granulocyte-CSF (G-CSF) were first identified as in vitro hematopoietic growth factors. They have since been shown to regulate myeloid cell numbers and function at steady state and during inflammation. Preclinical data suggest that targeting CSFs might be beneficial in autoimmune and inflammatory disease, and manipulation of CSF biology is now being tested in clinical trials. Here, we examine recent insights into CSF function, at steady state and during pathology, as provided by CSF or CSF receptor neutralization/deletion studies or from CSF administration. We discuss controversies regarding the role of CSFs in controlling specific myeloid cell populations and highlight how the newly identified M-CSF receptor ligand, interleukin (IL)-34, is necessitating a reassessment of the field.
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