Expression pattern and cellular sources of chemokines in primary central nervous system lymphoma

被引:77
作者
Brunn, Anna
Montesinos-Rongen, Manuel
Strack, Andreas
Reifenberger, Guido
Mawrin, Christian
Schaller, Carlo
Deckert, Martina
机构
[1] Univ Cologne, Abt Neuropathol, D-50924 Cologne, Germany
[2] Univ Dusseldorf, Inst Neuropathol, D-4000 Dusseldorf, Germany
[3] Univ Jena, Abt Neuropathol, D-6900 Jena, Germany
[4] Univ Bonn, Neurochirurg Klin, D-5300 Bonn, Germany
关键词
PCNSL; chemokines; astrocytes; microglia; cerebral endothelial cells;
D O I
10.1007/s00401-007-0258-x
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
The expression pattern of a subset of chemokines and their corresponding receptors was investigated in primary central nervous system lymphomas (PCNSL). The tumor cells consistently expressed CXCR4, CXCL12, CXCR5, and CXCL13, both at mRNA and protein levels. Cerebral endothelial cells were positive for CXCL12 and CXCL13, while reactive astrocytes and microglial cells expressed CXCL12, CCR5, and CCR6. Inflammatory T cells in PCNSL were characterized by CCR5 and CCR6 positivity. Taken together, our data indicate a cell type-specific repertoire of chemokine and chemokine receptor expression in PCNSL suggesting that chemokine-mediated interactions facilitate crossing of the blood-brain barrier as well as intracerebral dissemination of PCNSL cells. In addition, chemokines expressed by tumor cells may contribute to induction of reactive glial changes and influence the composition of inflammatory infiltrates in PCNSL. Therefore, cell type specific expression of distinct chemokine profiles likely plays a role in the pathogenesis of PCNSL and may contribute to their characteristic histological appearance.
引用
收藏
页码:271 / 276
页数:6
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