Identification and isolation of rat bone marrow-derived mast cells using the mast cell-specific monoclonal antibody AA4

被引:25
作者
Jamur, MC
Grodzki, ACG
Moreno, AN
de Mello, LD
Pastor, MVD
Berenstein, EH
Siraganian, RP
Oliver, C
机构
[1] Univ Sao Paulo, Fac Med Ribeirao Preto, Dept Morfol, BR-14049900 Ribeirao Preto, SP, Brazil
[2] Univ Fed Parana, Dept Biol Celular, BR-80060000 Curitiba, Parana, Brazil
[3] Natl Inst Dent & Craniofacial Res, Oral Infect & Immun Branch, NIH, Bethesda, MD USA
关键词
mast cells; gangliosides; maturation; bone marrow; immunochemistry; rat;
D O I
10.1177/002215540104900209
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Previous studies of mast cell maturation, structure, and function have been hampered by the lack of mast cell-specific markers. In this study, using a well-characterized mast cell-specific monoclonal antibody, MAb AA4, mast cells from rat bone marrow in various stages of maturation were isolated and characterized. The very immature mast cells, which have not been previously described, contained few granules and would not be recognized as mast cells by standard cytological methods. Pure populations of mast cells were isolated from the bone marrow using MAb AA4-conjugated magnetic beads. The same stages of maturation were observed in the isolated mast cells as were seen in the unfractionated bone marrow. All of these cells were immunopositive for the alpha -subunit of Fc epsilon RI, IgE, and c-kit, confirming their identity as mast cells. By direct counting of immunolabled cells and by flow cytometry, approximately 2.4% of the cells in the bone marrow are mast cells. Staining with toluidine blue and berberine sulfate, as well as RT-PCR of the cells, indicates that these cells are connective tissue-type mast cells. The use of immunological methods for identification of mast cell precursors should facilitate the study of these cells.
引用
收藏
页码:219 / 228
页数:10
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