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Blood, 1 July 2005, Vol. 106, No. 1, pp. 384-385.
CORRESPONDENCE To the editor:Expression of the chemokine receptors CXCR4, CXCR5, and CCR7 in primary central nervous system lymphomaPrimary central nervous system lymphoma (PCNSL) is a rare form of non-Hodgkin lymphoma (NHL) that is confined to the central nervous system (CNS) at the time of diagnosis.1 There are 2 unresolved questions: why PCNSL involves the CNS, a site that contains very few resident B lymphocytes under physiologic conditions, and why systemic spread is rare. The expression of chemokine receptors on tumor cells plays an important role for their metastatic potential.2,3 Of particular interest for B-cell migration are the chemokine receptors CXC chemokine receptor 4 (CXCR4), CXCR5, and CC chemokine receptor 7 (CCR7), regulating migration into lymph nodes and other organs. Recently, expression of CXCR4, CXCR5, and CCR7 in low-grade B-cell NHL (B-NHL) and classical Hodgkin lymphoma4-8 and an association with lymph node involvement5,6 were reported. We have investigated the expression of CXCR4, CXCR5, and CCR7 in PCNSL and extracerebral lymphomas by immunohistochemistry and immunofluorescence microscopy, hypothesizing that the absence of systemic spread in PCNSL could be linked to reduced or absent expression of these chemokine receptors. A total of 29 PCNSL biopsy specimens obtained from HIV-negative patients, including 27 diffuse large B-cell lymphomas and 2 lymphoplasmacytic lymphomas, and 29 peripheral B-NHL specimens, including 17 diffuse large B-cell lymphomas, 6 mantle cell lymphomas, and 6 chronic lymphocytic lymphomas, were immunostained. Functionality of chemokine receptor expression was analyzed on lymphoma cell lines by transwell migration assays. In contrast to our expectations, CXCR4, CXCR5, and CCR7 expression was observed in the neoplastic cells of all 29 PCNSL specimens. Positivity for all chemokine receptors was, however, restricted to the cytoplasm and, in some cases, to the nucleus (CXCR4); no clear membranous staining was observed (Figure 1A shows an example of CXCR4). CXCR4 and CCR7 cytoplasmic location was confirmed by immunofluorescence microscopy (Figure 1B-C shows an example of CXCR4). In contrast, both membranous and cytoplasmic expression of CXCR4, CXCR5, and/or CCR7 were observed in 11, 11, and 14, respectively, of the 29 peripheral B-cell lymphomas (Figure 1D-F shows an example of CXCR4), in agreement with previous reports.4-8 As PCNSL cell lines have not yet been established, potential functionality of cytoplasmic CCR7 and CXCR4 could be analyzed only on peripheral lymphoma cell lines. The lymphoma cell lines Raji and YT, demonstrating intracellular but no surface CCR7 and CXCR4 expression, respectively, showed no chemotactic response to the specific ligands CC chemokine ligand 19/21 (CCL19/21) and stromal cell-derived factor 1 (SDF-1), respectively, in contrast to cell lines with membranous expression (data not shown). Taken together, CXCR4, CXCR5, and CCR7 expression in PCNSL is restricted to the cytoplasm, in sharp contrast to a large proportion of peripheral lymphomas. As chemokine receptor down-regulation occurs during B-cell differentiation,9 PCNSL may represent a malignant variant of differentiated B cells, which physiologically down-regulate surface CXCR4, CXCR5, and CCR7. Our functional studies in lymphoma cell lines suggest that the cytoplasmic location of chemokine receptors in PCNSL interferes with its function in cell migration, which may be the underlying mechanism for the low propensity of PCNSL to disseminate extracerebrally. This hypothesis is supported by a murine lymphoma model, revealing that retention of CXCR4 in the endoplasmatic reticulum results in prevention of dissemination.10
Correspondence: Kristoph Jahnke, Department of Hematology, Oncology and Transfusion Medicine, Charité-Universitätsmedizin Berlin, Campus Benjamin Franklin, Hindenburgdamm 30, D-12200 Berlin, Germany; e-mail: kristoph.jahnke{at}charite.de From the Department of Hematology, Oncology and Transfusion Medicine, the Department of General Pathology and Reference Center for Hematopathology, Charité-Universitätsmedizin Berlin, Campus Benjamin Franklin, Germany.
K.J.: designed research, performed research, analyzed data, wrote the paper; SEC.: performed research, contributed vital analytical tools, analyzed data, wrote the paper; I.-K.N.: performed research; C.L.: performed research, contributed vital analytical tools; U.K.: designed research; A.K.: analyzed data; H.S.: analyzed data; E.T.: designed research, analyzed data; C.S.: designed research, contributed vital analytical tools, analyzed data, wrote the paper.
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| Copyright © 2005 by American Society of Hematology Online ISSN: 1528-0020 | |||||||||
4 integrin are important for migration of chronic lymphocytic leukemia cells into lymph nodes. Blood. 2002;99: 2977-2984.
