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Monocyte CD14: a multifunctional receptor engaged in apoptosis from both sides
1Department of Medicine, University of Münster, Germany. heidenr@uni-muenster.de
Journal of Leukocyte Biology
|June 25, 1999
Summary
Monocyte apoptosis is induced by interleukin-4 (IL-4) and linked to CD14 receptor changes. Macrophages resist apoptosis, a trait potentially beneficial in inflammation and phagocytosis.
Area of Science:
- Immunology
- Cell Biology
Background:
- Monocytes and macrophages, key immune cells, can undergo apoptosis due to triggers, mediators, or aging.
- Mechanisms of apoptosis are better understood in lymphocytes than in monocytes/macrophages.
Purpose of the Study:
- To investigate the factors and mechanisms of monocyte and macrophage apoptosis.
- To explore the role of the CD14 receptor in regulating apoptosis in these cells.
Main Methods:
- Investigated the effects of Th2 cell-derived cytokines, specifically interleukin-4 (IL-4), on monocyte apoptosis.
- Examined the role of the CD14 surface receptor in apoptosis regulation.
- Compared apoptosis sensitivity between monocytes and macrophages.
Main Results:
- Interleukin-4 (IL-4) effectively induces monocyte apoptosis, preceded by CD14 down-regulation.
- Lipopolysaccharide (LPS) suppresses apoptosis and up-regulates CD14.
- Macrophages exhibit significant resistance to apoptosis compared to monocytes.
- The CD14 receptor appears to play a dual role in promoting survival and antagonizing apoptosis in monocytes, and in facilitating interaction with apoptotic cells in macrophages.
Conclusions:
- Monocyte apoptosis is modulated by cytokines like IL-4 and influenced by CD14 expression levels.
- Macrophages' resistance to apoptosis is crucial for their phagocytic function in inflammatory settings.
- The CD14 receptor is a key player in the apoptotic network of both monocytes and macrophages.