Brunn Anna, Montesinos-Rongen Manuel, Strack Andreas, Reifenberger Guido, Mawrin Christian, Schaller Carlo, Deckert Martina
Abteilung für Neuropathologie, Universität zu Köln, Kerpener Str. 62, 50924, Köln, Germany.
Acta Neuropathol. 2007 Sep;114(3):271-6. doi: 10.1007/s00401-007-0258-x. Epub 2007 Jul 20.
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.
在原发性中枢神经系统淋巴瘤(PCNSL)中研究了趋化因子及其相应受体的一个亚群的表达模式。肿瘤细胞在mRNA和蛋白质水平上均持续表达CXCR4、CXCL12、CXCR5和CXCL13。脑内皮细胞对CXCL12和CXCL13呈阳性,而反应性星形胶质细胞和小胶质细胞表达CXCL12、CCR5和CCR6。PCNSL中的炎性T细胞以CCR5和CCR6阳性为特征。综上所述,我们的数据表明PCNSL中趋化因子和趋化因子受体表达具有细胞类型特异性,提示趋化因子介导的相互作用促进了血脑屏障的穿越以及PCNSL细胞的脑内播散。此外,肿瘤细胞表达的趋化因子可能有助于诱导反应性胶质细胞变化,并影响PCNSL中炎性浸润的组成。因此,不同趋化因子谱的细胞类型特异性表达可能在PCNSL的发病机制中起作用,并可能导致其特征性组织学表现。