Blaheta Roman A, Hundemer Michael, Mayer Gottfried, Vogel Jens-Uwe, Kornhuber Bernhard, Cinatl Jaroslav, Markus Bernd H, Driever Pablo Hernáiz, Cinatl Jindrich
Zentrum der Hygiene, Institut für Medizinische Virologie, Klinikum der J. W Goethe-Universität, Frankfurt am Main, Germany.
Cell Commun Adhes. 2002 May-Jun;9(3):131-47. doi: 10.1080/15419060214520.
The precise function of cell adhesion molecules in the hematogenous phase of neuroblastoma metastasis is poorly understood. The aim of this study was to investigate whether neural cell adhesion molecule (NCAM) modulates neuroblastoma cell (NB) adhesion and transendothelial penetration in a coculture model. Our data, assessed on 11 NB cell lines, demonstrate an inverse correlation between NCAM expression and NB cell adhesion. Transfection of the NB cell line UKF-NB-4 with a cDNA encoding the human NCAM-140 kD isoform enhanced NCAM expression and the amount of tumor cell aggregates, reduced the amount of single tumor cells, and diminished initial NB cell adhesion to an endothelial cell monolayer. Treatment of UKF-NB-4 with NCAM antisense oligonucleotides reduced NCAM surface level, increased the number of single tumor cells, and induced up-regulation of NB cell adhesion to endothelium. Modulation of NCAM expression had no effect on transendothelial penetration. Fluorescence analysis revealed a down-regulation of NCAM in single tumor cells, prior to NB adhesion. The data support the view that low levels of NCAM are necessary for NB cells to leave a tumor cell aggregate and adhere to endothelial cells.
神经母细胞瘤转移血行期细胞黏附分子的确切功能尚不清楚。本研究的目的是在共培养模型中研究神经细胞黏附分子(NCAM)是否调节神经母细胞瘤细胞(NB)的黏附和跨内皮穿透。我们对11种NB细胞系进行评估的数据表明,NCAM表达与NB细胞黏附呈负相关。用编码人NCAM-140 kD异构体的cDNA转染NB细胞系UKF-NB-4可增强NCAM表达和肿瘤细胞聚集体数量,减少单个肿瘤细胞数量,并减少NB细胞对内皮细胞单层的初始黏附。用NCAM反义寡核苷酸处理UKF-NB-4可降低NCAM表面水平,增加单个肿瘤细胞数量,并诱导NB细胞对内皮细胞黏附上调。NCAM表达的调节对跨内皮穿透没有影响。荧光分析显示,在NB黏附之前,单个肿瘤细胞中的NCAM表达下调。这些数据支持这样一种观点,即低水平的NCAM对于NB细胞离开肿瘤细胞聚集体并黏附于内皮细胞是必要的。