Abstract
The recently identified ligand for C-kit, a protooncogene encoded by the Wlocus in mice, is a member of the tyrosine kinase receptor family with growth factor activity for mouse mast cells. Mature human mast cells regularly develop from agranular precursors in cord blood in long-term cocultures of cord blood and murine fibroblasts. Since the c-kit ligand is a product of murine fibroblasts, wc examined the growth effect of recombinant human c-kit ligand (stem cell factor), of recombinant murine c-kit ligand (mast cell growth factor), and of a partially purified fraction derived from mouse fibroblast culture supernatant on the mast cell lineage of humans by electron microscopy in 8-week cultures of cord blood cells. We found thai immature mast cells which developed in cultures containing the recombinant ligand for c-kit of human or murine origin as well as the naturally occurring c-kit ligand in.YI3 fibroblast supernatants were identical. Thus, each of these sources of the c-kil ligand exerted identical effects on the ontogeny of human mast cells as they develop from their agranular precursors in cord blood. Full maturity of factor-supported mast cells did not occur.
Original language | English (US) |
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Pages (from-to) | 247-253 |
Number of pages | 7 |
Journal | International archives of allergy and immunology |
Volume | 101 |
Issue number | 3 |
DOIs | |
State | Published - 1993 |
Externally published | Yes |
Keywords
- Cord blood
- Infrastructure
- Mast cell growth factor
- Mast cell, human
- Stem cell factor
- c-kit ligand
ASJC Scopus subject areas
- Immunology and Allergy
- Immunology