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Proliferation and Differentiation of Murine Myeloid Precursor 32D/G-CSF-R Cells
Published on: February 21, 2018
Expression of GM-CSF receptor by Langerhans' cell histiocytosis cells
J F Emile1, S Fraitag, P Andry
1Service d'anatomie et de cytologie pathologiques, Hôpital Necker-Enfants Malades, Paris, France.
Insights
Langerhans' cell histiocytosis (LCH) involves abnormal cell growth. This study found that LCH cells express the granulocyte/macrophage colony-stimulating factor (GM-CSF) receptor, suggesting GM-CSF may drive LCH proliferation.
Area of Science:
- Immunology
- Hematology
- Oncology
Background:
- Langerhans' cell histiocytosis (LCH) is a clonal disorder characterized by CD1a-positive cell proliferation.
- The exact cause of LCH remains unknown, although cytokines are known to control cell growth and differentiation.
Purpose of the Study:
- To investigate the potential role of granulocyte/macrophage colony-stimulating factor (GM-CSF) in LCH pathogenesis.
- To determine the presence of the GM-CSF receptor on LCH cells.
Main Methods:
- In situ immunohistochemistry was performed on 14 frozen LCH tissue samples.
- Two mouse monoclonal antibodies targeting the alpha chain of the GM-CSF receptor (CDw116) were used.
Main Results:
- LCH cells from all 14 samples showed positive staining for the GM-CSF receptor (CDw116).
- LCH cells were found to contain GM-CSF, and elevated serum levels were observed in disseminated LCH.
Conclusions:
- The presence of the GM-CSF receptor on LCH cells suggests that GM-CSF may function as a growth factor for these cells.
- These findings implicate GM-CSF in the pathogenesis of Langerhans' cell histiocytosis.
Abstract:
Langerhans' cell histiocytosis (LCH) is characterized by the proliferation of large mononucleated cells containing Birbeck granules and expressing CD1a. Recent studies have demonstrated that LCH is a clonal proliferation; however, its aetiology is still unknown. Growth and differentiation of bone-marrow-derived cells are controlled by cytokines. The proliferation, differentiation and activation of normal Langerhans cells are controlled by granulocyte/macrophage colony-stimulating factor (GM-CSF) in vitro. Therefore, GM-CSF could be implicated in the pathogenesis of LCH. Indeed, LCH cells contain GM-CSF, and children with disseminated LCH have an elevated GM-CSF serum level. As a cytokine only acts on cells expressing a specific receptor, we investigated the presence of GM-CSF receptor on LCH cells. Fourteen frozen tissue samples from children with LCH were studied by in situ immunohistochemistry with two mouse monoclonal antibodies specific for the alpha chain of the GM-CSF receptor (CDw116). LCH cells of all the samples were positively stained with both antibodies. This study suggests that GM-CSF may be a growth factor for LCH cells.
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