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肿瘤坏死因子-α诱导人神经母细胞瘤细胞黏附/分化需要诱导型一氧化氮合酶的表达。

Induction of adhesion/differentiation of human neuroblastoma cells by tumour necrosis factor-alpha requires the expression of an inducible nitric oxide synthase.

作者信息

Obregón E, Punzón M C, González-Nicolás J, Fernandez-Cruz E, Fresno M, Muñoz-Fernández M A

机构信息

Department of Immunology, Hospital Universitario General Gregorio Marañon, Madrid, Spain.

出版信息

Eur J Neurosci. 1997 Jun;9(6):1184-93. doi: 10.1111/j.1460-9568.1997.tb01473.x.

DOI:10.1111/j.1460-9568.1997.tb01473.x
PMID:9215702
Abstract

Neuroblastoma cell lines (SK-N-SH and SK-N-MC) were induced to differentiate, as detected by the expression of neurofilament proteins of 68 and 200 kDa, and to express adhesion molecules (intercellular adhesion molecule-1 and vascular cell adhesion molecule) after stimulation with tumour necrosis factor-alpha (TNF-alpha). This induction was accompanied by the arrest of cell growth. The induction of neuroblastoma adhesion by TNF-alpha could be inhibited by the nitric oxide synthase inhibitors, L-N-monomethyl arginine (L-NMMA) and L-N6-(1-imidoethyl)-lysine (highly specific for the inducible enzyme), but not by the inactive enantiomer D-NMMA. These results indicate that TNF-alpha induces the adhesion of neuroblastoma cells via nitric oxide. This was confirmed by the finding that the adhesion/differentiation of SK-N-SH and SK-N-MC cells can be directly induced by the addition of nitric oxide donors, sodium nitroprusside and S-nitroso-N-acetyl-penicillamine, into the culture medium. The isoform of the nitric oxide synthase induced in human neuroblastoma cells by TNF-alpha treatment was identified enzymatically as isoform II by Western blotting and by the polymerase chain reaction. Thus TNF-alpha induces the in vitro adhesion/differentiation of human neuroblastoma cells through nitric oxide synthesized by a calcium-independent inducible form of nitric oxide synthase, clearly indicating that isoform II of nitric oxide synthase can be expressed in human neuronal cell types.

摘要

神经母细胞瘤细胞系(SK-N-SH和SK-N-MC)经诱导后发生分化,可通过68 kDa和200 kDa神经丝蛋白的表达检测到,并且在用肿瘤坏死因子-α(TNF-α)刺激后表达黏附分子(细胞间黏附分子-1和血管细胞黏附分子)。这种诱导伴随着细胞生长的停滞。TNF-α对神经母细胞瘤黏附的诱导作用可被一氧化氮合酶抑制剂L-N-单甲基精氨酸(L-NMMA)和L-N6-(1-亚氨基乙基)-赖氨酸(对诱导型酶具有高度特异性)抑制,但不能被无活性对映体D-NMMA抑制。这些结果表明,TNF-α通过一氧化氮诱导神经母细胞瘤细胞黏附。通过在培养基中添加一氧化氮供体硝普钠和S-亚硝基-N-乙酰青霉胺可直接诱导SK-N-SH和SK-N-MC细胞的黏附/分化,这一发现证实了上述结论。通过蛋白质印迹法和聚合酶链反应酶促鉴定,TNF-α处理诱导人神经母细胞瘤细胞中产生的一氧化氮合酶同工型为同工型II。因此,TNF-α通过由钙非依赖性诱导型一氧化氮合酶合成的一氧化氮诱导人神经母细胞瘤细胞的体外黏附/分化,清楚地表明一氧化氮合酶同工型II可在人神经元细胞类型中表达。

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