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PMID: 16342298 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Review

Evidence of abortive plasma cell differentiation in Hodgkin and Reed-Sternberg cells of classical Hodgkin lymphoma.

Hematological oncology ·Vol. 23 ·No. 3-4 ·2005-00-00 ·Pages 127-32

Buettner M, Greiner A, Avramidou A, Jäck HM, Niedobitek G

Abstract

Hodgkin and Reed-Sternberg (HRS) cells of classical Hodgkin lymphoma (cHL) show genotypic features of germinal centre-derived B-cells in most cases. Nevertheless, these cells typically lack expression of B-cell antigens. Previous studies have suggested that plasma cell differentiation may occur in HRS cells and that this may account for the down-regulation of B-cell antigens. However, these results are controversial. We have addressed this question using immunohistochemistry and a panel of antibodies directed against antigens which are differentially expressed during terminal B-cell differentiation. Pax-5, a transcription factor required for B-lineage commitment, and IRF4/Mum1, which is physiologically expressed in germinal centre cells and plasma cells, were consistently detectable in HRS cells. Bcl-6, a transcription factor expressed in germinal centre B-cells, was present in HRS cells of approximately 25% of cHL cases. Expression of the B-lymphocyte-induced maturation protein-1 (Blimp-1), a key regulator of plasma cell differentiation, was observed in HRS cells of 23% of cHL cases. In these cases, Blimp-1 expression was restricted to a small proportion of HRS cells. HRS cells were consistently negative for the plasma cell marker CD138. These results suggest that plasma cell differentiation may be initiated in a small subset of HRS cells but remains abortive. Thus, terminal differentiation is unlikely to explain the lack of B-cell antigen expression in HRS cells.

MeSH Terms
Cell Transformation, Neoplastic/metabolism,pathology Gene Expression Regulation, Leukemic Hodgkin Disease/metabolism,pathology Humans Immunohistochemistry Membrane Glycoproteins/biosynthesis Neoplasm Proteins/biosynthesis Plasma Cells/metabolism,pathology Proteoglycans/biosynthesis Reed-Sternberg Cells/metabolism,pathology Syndecan-1 Syndecans Transcription Factors/biosynthesis
Chemicals
Membrane Glycoproteins Neoplasm Proteins Proteoglycans SDC1 protein, human Syndecan-1 Syndecans Transcription Factors
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Buettner Maike
Institute for Pathology, Department of Internal Medicine III, Nikolaus-Fiebiger-Center, Friedrich-Alexander-University, Erlangen, Germany. maike.buettner@patho.imed.uni-erlangen.de
Greiner Axel
Avramidou Athanasia
Jäck Hans-Martin
Niedobitek Gerald
Article Info
Journal
Hematological oncology
Abbr.
Hematol Oncol
ISSN
0278-0232
Published
2005-00-00
Pages
127-32
Language
English
Region
England
NLM ID
8307268
Subset
IM
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