Immunolocalization of the ICE/Ced-3-family protease, CPP32 (Caspase-3), in non-Hodgkin's lymphomas, chronic lymphocytic leukemias, and reactive lymph nodes

被引:85
作者
Krajewski, S
Gascoyne, RD
Zapata, JM
Krajewska, M
Kitada, S
Chhanabhai, M
Horsman, D
Berean, K
Piro, LD
FugierVivier, I
Liu, YJ
Wang, HG
Reed, JC
机构
[1] LA JOLLA CANC RES FDN,CANC RES CTR,BURNHAM INST,LA JOLLA,CA 92037
[2] BRITISH COLUMBIA CANC AGCY,DEPT PATHOL,VANCOUVER,BC V5Z 4E6,CANADA
[3] VANCOUVER HOSP & HLTH SCI CTR,DEPT PATHOL,VANCOUVER,BC V5Z 1M9,CANADA
[4] SCRIPPS CLIN,GREENE CANC CTR,LA JOLLA,CA
[5] SHERING PLOUGH INC,CTR RECH,DARDILLY,FRANCE
关键词
D O I
10.1182/blood.V89.10.3817.3817_3817_3825
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Immunohistochemical analysis of the apoptosis-effector protease CPP32 (Caspase-3) in normal lymph nodes, tonsils, and nodes affected with reactive hyperplasia (n = 22) showed strong immunoreactivity in the apoptosis-prone germinal center B-lymphocytes of secondary follicles, but little or no reactivity in the surrounding long-lived mantle zone lymphocytes. Immunoblot analysis of fluorescence-activated cell sorted germinal center and mantle zone B cells supported the immunohistochemical results. In 22 of 27 (81%) follicular small cleaved cell non-Hodgkin's B-cell lymphomas, the CPP32-immunopositive germinal center lymphocytes were replaced by CPP32-negative tumor cells. In contrast, the large cell component of follicular mixed cells (FMs) and follicular large cell lymphomas (FLCLs) was strongly CPP32 immunopositive in 12 of 17 (71%) and in 8 of 14 (57%) cases, respectively, whereas the residual small-cleaved cells were poorly stained for CPP32 in all FLCLs and in 12 of 17 (71%) FMs, suggesting that an upregulation of CPP32 immunoreactivity occurred during progression. Similarly, cytosolic immunostaining for CPP32 was present in 10 of 12 (83%) diffuse large cell lymphomas (DLCLs) and 2 of 3 diffuse mixed B-cell lymphomas (DMs). Immunopositivity for CPP32 was also found in the majority of other types of non-Hodgkin's lymphomas studied. Plasmacytomas were CPP32 immunonegative in 4 of 12 (33%) cases, in contrast to normal plasma cells, which uniformly contained intense CPP32 immunoreactivity, implying downregulation of CPP32 in a subset of these malignancies. All 12 peripheral blood B-cell chronic lymphocyte leukemia specimens examined were CPP32 immunopositive, whereas 3 of 3 small lymphocytic lymphomas were CPP32 negative, suggesting that CPP32 expression may vary depending on the tissue compartment in which these neoplastic B cells reside. The results show dynamic regulation of CPP32 expression in normal and malignant lymphocytes. (C) 1997 by The American Society of Hematology.
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页码:3817 / 3825
页数:9
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