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Updated: Aug 8, 2026

Analyzing the Functions of Mast Cells In Vivo Using 'Mast Cell Knock-in' Mice
Published on: May 27, 2015
The c-kit ligand, stem cell factor, promotes mast cell survival by suppressing apoptosis
Abstract:
Stem cell factor (SCF) and its receptor (SCFR), a member of the receptor tyrosine kinase III family that is encoded by the c-kit gene, critically regulate several complex biological programs including hematopoiesis, mast cell development, cutaneous pigmentation, and gametogenesis. We show herein that mouse mast cells die rapidly after the withdrawal of SCF in vivo or in vitro, and provide morphological evidence that such mast cells undergo programmed cell death or apoptosis. We also show that when in vitro-derived mouse mast cells maintained in SCF are removed from SCF-containing medium for only 5 or 6 hours, the cells' genomic DNA exhibits the ladder-like pattern of oligonucleosome-sized fragments typical of apoptosis. These findings demonstrate that SCF can regulate the survival of a cellular lineage which expresses the SCFR by suppressing apoptosis. They also identify a mechanism that can result in striking and rapid reductions in the size of tissue mast cell populations without histological evidence of the concomitant induction of a significant inflammatory response.
Insights
Stem cell factor (SCF) regulates mast cell survival by preventing apoptosis. Withdrawal of SCF triggers rapid programmed cell death in mast cells, impacting tissue populations.
Area of Science:
- Cell biology
- Molecular biology
- Immunology
Background:
- Stem cell factor (SCF) and its receptor (SCFR), encoded by the c-kit gene, are crucial for hematopoiesis, mast cell development, pigmentation, and gametogenesis.
- SCF belongs to the receptor tyrosine kinase III family.
Purpose of the Study:
- To investigate the role of SCF in mast cell survival.
- To determine if mast cell death upon SCF withdrawal involves apoptosis.
Main Methods:
- In vivo and in vitro experiments involving mouse mast cells.
- Morphological analysis of mast cells after SCF withdrawal.
- DNA fragmentation analysis (DNA laddering) to detect apoptosis.
Main Results:
- Mouse mast cells undergo rapid death upon SCF withdrawal, both in vivo and in vitro.
- Morphological and DNA fragmentation evidence indicates programmed cell death (apoptosis).
- Apoptotic DNA fragmentation was observed within 5-6 hours of SCF removal in vitro.
Conclusions:
- SCF suppresses apoptosis, thereby regulating the survival of mast cells expressing SCFR.
- This mechanism explains rapid mast cell population reductions without significant inflammation.
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