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

Trends in Immunology
|September 25, 2012
PubMed

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.

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