The American Journal of Surgical Pathology · 2001 · 20 citations · 32 references
Life SciencesMolecular BiologyPathologyCell ProliferationCell SignalingSignal TransductionB Cell ActivationB Cell BiologyLymphocyte ActivationLymphoid NeoplasmsLymphoid TissueLymphoid TumorsCell ActivationImmunohistochemical BiomarkersImmunohistochemical DetectionImmunohistochemical Staining
SHP-1 is a protein phosphotyrosine phosphatase that plays an important role in modulating intracellular signaling, which regulates cell activation, proliferation, differentiation, and migration. It is a negative regulator of signal transduction induced by a number of cell receptors. Our immunohistochemical examination of paraffin-embedded reactive lymph nodes and lymphoid tissues revealed that B lymphocytes in follicle germinal centers do not express SHP-1. A weak staining of the B cells in the germinal center light zones was detected when an ultrasensitive amplification system was used. In contrast, normal B cells in mantle and marginal zones as well as interfollicular B lymphocytes and plasma cells displayed strong immunoreactivity. This pattern of SHP-1 expression was repeated in small B-cell lymphomas. All cases of mantle cell lymphoma (12 of 12), marginal zone lymphoma (10 of 10), and chronic lymphocytic leukemia/small lymphocytic lymphoma (13 of 13) expressed SHP-1 protein. However, only 1 of 30 cases of grade 1 follicle center cell lymphoma expressed SHP-1. Our observations highlight the biologic functions of SHP-1 and demonstrate that the SHP-1 expression pattern by small B-cell lymphomas reflects the maturation stage of their normal cell counterparts. These results indicate that determination of SHP-1 expression may help in the differential diagnosis of small B-cell lymphomas.
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Recruitment of Tyrosine Phosphatase HCP by the Killer Cell Inhibitory Receptor
Deborah N. Burshtyn, Andrew M. Scharenberg, Nicolai Wagtmann et al. · Immunity · 1996 · 615 citations · Full text
Activation of a Phosphotyrosine Phosphatase by Tyrosine Phosphorylation
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Hyperresponsive B Cells in CD22-Deficient Mice
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