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Leukemia ; 19(6): 1018-24, 2005 Jun.
Article in English | MEDLINE | ID: mdl-15800671

ABSTRACT

The Syk family tyrosine kinase ZAP-70 is essential for normal T-cell development and signaling. Recently, leukemic cells from some patients with B-cell chronic lymphocytic leukemia (B-CLL) were shown to express ZAP-70. Owing to the prognostic value of B-CLL ZAP-70 expression, this phenotype may reflect intrinsic biological differences between the two subsets of disease. However, it remains unclear whether CLL-B cells aberrantly acquire ZAP-70 expression during the transformation process or whether ZAP-70 may be expressed under certain conditions in normal human B-lymphocytes. To discriminate between these two possibilities, we assessed ZAP-70 expression in normal human B-lymphocytes. Our data demonstrate that ZAP-70 is expressed in a subpopulation of tonsillar and splenic normal B-lymphocytes that express an activated phenotype. Furthermore, ZAP-70 expression can be induced in vitro upon stimulation of blood and tonsillar B cells. Finally, we show that phosphorylation of ZAP-70 occurs in tonsillar B cells with stimulation through the B-cell receptor. These results provide new insight into normal human B-cell biology as well as provide clues about the transformed cell in B-CLL.


Subject(s)
B-Lymphocytes/physiology , Lymphocyte Activation/physiology , Lymphocyte Subsets/physiology , Protein-Tyrosine Kinases/genetics , Cell Differentiation/immunology , Flow Cytometry , Humans , Jurkat Cells , Palatine Tonsil/cytology , Phenotype , Phosphorylation , Protein-Tyrosine Kinases/metabolism , Spleen/cytology , Transfection , ZAP-70 Protein-Tyrosine Kinase
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