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Cysteine protease CPP32, but not Ich 1-L, is expressed in germinal center B cells and their neoplastic counterparts

Ich-1/Nedd2 and CPP32/YAMA are cysteine proteases related to interleukin 1-β-converting enzyme (ICE), which act as apoptosis effectors. Both molecules are expressed in T- and B-cell lines. The authors investigated their in vivo cellular distribution in normal and neoplastic human lymphoid tissues. S...

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Published in:Human pathology 1997-08, Vol.28 (8), p.912-921
Main Authors: Xerri, Luc, Devilard, Elisabeth, Ayello, Corinne, Brousset, Pierre, Reed, John C, Emile, Jean-François, Hassoun, Jacques, Parmentier, Sophie, Birg, Françoise
Format: Article
Language:English
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Summary:Ich-1/Nedd2 and CPP32/YAMA are cysteine proteases related to interleukin 1-β-converting enzyme (ICE), which act as apoptosis effectors. Both molecules are expressed in T- and B-cell lines. The authors investigated their in vivo cellular distribution in normal and neoplastic human lymphoid tissues. Sixty-eight representative non-Hodgkin's lymphomas (NHL) and Hodgkin's disease (HD) samples, normal lymphoid organs, and nonlymphoid tumors were analyzed by immunohistochemistry (IHC). CPP32 expression in benign tissues was restricted to germinal center B cells, plasma cells, and a few interfollicular immunoblasts. All follicular NHLs and most diffuse large cell NHLs were CPP32 positive. Among T-cell NHLs, CPP32 expression was mainly observed in anaplastic large cell NHLs, whereas the other subtypes were less frequently positive. In contrast, lymphoid organs displayed only weak Ichl-L expression, located in sinusal histiocytes and thymic epithelial cells. Lymphomas were Ich1L negative, except for T-cell-rich B-cell NHLs, and about half of the HD samples, in which Reed-Sternberg cells (RSC) were usually Ich1L positive/CPP32 negative. Extralymphoid Ichl-L reactivity was found in particular organs like the kidney and various tumors. Western blot analysis confirmed the specificity of immunostaining. Neither CPP32 nor Ichl-L expression were correlated with intratumoral DNA fragmentation, as determined by the TUNEL assay. Altogether, these results indicate that CPP32 is preferentially expressed in germinal centers and thus could be involved in B-cell maturation. The differential expression of CPP32 and Ich1-L suggests that cysteine proteases differ in substrate specificities and carry out functions unrelated to apoptosis.
ISSN:0046-8177
1532-8392
DOI:10.1016/S0046-8177(97)90006-X