Analysis of the lineage relationship between mast cells and basophils using the c- kit D816V mutation as a biologic signature

• Published in: Journal of Allergy and Clinical Immunology 2005-06, Vol.115 (6), p.1155-1161
• Main Authors: Kocabas, Can N., Yavuz, Akif S., Lipsky, Peter E., Metcalfe, Dean D., Akin, Cem
• Format: Article
• Language: English
• Subjects: basophils; Basophils - immunology; Basophils - metabolism; Biological and medical sciences; c-kit; Cell Lineage - genetics; Fundamental and applied biological sciences. Psychology; Fundamental immunology; hematopoiesis; Humans; Immunopathology; Mast cells; Mast Cells - immunology; Mast Cells - metabolism; mastocytosis; Mastocytosis - blood; Mastocytosis - genetics; Mastocytosis - immunology; Medical sciences; Mutation; Polymorphism, Restriction Fragment Length; Stem Cell Factor - analysis; Stem Cell Factor - genetics; Stem Cell Factor - metabolism
• ISSN: 0091-6749; 1097-6825; 1365-2567
• DOI: 10.1016/j.jaci.2005.02.030

Mast cells and basophils share similar morphologic and functional properties; however, it is not known whether they are derived from a bilineage (basophil/mast cell)–restricted progenitor. To assess whether basophils and mast cells are derived from common committed progenitors using the c- kit D816V mutation as a biologic signature. The D816V c- kit mutation found in mast cells of patients with systemic mastocytosis is used as a trackable genetic marker to assess the lineage relationship between mast cells and basophils. Blood and bone marrow aspirates were collected from 33 consecutive patients with mastocytosis with different disease severity. Peripheral blood basophils, monocytes and neutrophils were sorted by immunomagnetic beads. Presence of the D816V c- kit mutation was analyzed by restriction fragment length polymorphism in the genomic DNA and mRNA from sorted cells in all patients and in the genomic DNA of individual basophils of 1 patient. The c- kit D816V mutation was detectable in basophils of 5 patients (15%). All 5 patients had the c- kit mutation also detectable in monocytes and thus had multilineage involvement. Single cell analysis of the genomic DNA in 1 patient showed a similar degree of clonal expansion in basophils, monocytes, and neutrophils. Mutated c- kit was expressed at the mRNA level in all 5 patients. There was no difference in surface Kit expression levels in basophils. Basophils carrying the D816V c- kit mutation in mastocytosis were detected only in the context of a multilineage involvement. These results argue against the presence of a bilineage-restricted committed progenitor for mast cells and basophils.