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胶质瘤细胞诱导微血管内皮细胞发生血管生成,而肿瘤坏死因子在体外对其有抑制作用。

Angiogenesis in microvascular endothelial cells induced by glioma cells and inhibited by tumor necrosis factor in vitro.

作者信息

Niida H, Takeuchi S, Tanaka R, Minakawa T

机构信息

Department of Neurosurgery, Niigata University, Japan.

出版信息

Neurol Med Chir (Tokyo). 1995 Apr;35(4):209-14. doi: 10.2176/nmc.35.209.

Abstract

Neovascularization is a prerequisite for glioma growth, so inhibition of angiogenesis may achieve control of glioma growth. We examined whether glioma cells induce angiogenesis and proliferation in microvascular endothelial cells from Fisher 344 rat brains by co-culture in a physical separation system with rat C6 glioma cells or rat T9 gliosarcoma cells. Endothelial cells cultured on type 1 collagen formed capillary-like structures. C6 glioma cells co-cultured with endothelial cells promoted the formation of these capillary-like structures. However, conditioned medium from C6 cells inhibited the proliferation of endothelial cells. T9 cells had little effect on the formation of capillary-like structures and no effect on the proliferation of endothelial cells. We also examined the effects of human tumor necrosis factor (TNF)-alpha on the formation of the capillary-like structures and on the proliferation of endothelial cells. Human TNF-alpha inhibited the formation of capillary-like structures induced by C6 glioma cells at a concentration of 100 U/ml, as well as the proliferation of endothelial cells at a concentration of 1000 U/ml. These results indicate that induction of angiogenesis varies with glioma cell lines and angiogenesis does not correspond with proliferation of endothelial cells. TNF-alpha can inhibit angiogenesis in gliomas in vitro.

摘要

新生血管形成是胶质瘤生长的前提条件,因此抑制血管生成可能实现对胶质瘤生长的控制。我们通过在物理分离系统中与大鼠C6胶质瘤细胞或大鼠T9胶质肉瘤细胞共培养,研究了胶质瘤细胞是否诱导Fisher 344大鼠脑微血管内皮细胞的血管生成和增殖。在I型胶原上培养的内皮细胞形成了毛细血管样结构。与内皮细胞共培养的C6胶质瘤细胞促进了这些毛细血管样结构的形成。然而,C6细胞的条件培养基抑制了内皮细胞的增殖。T9细胞对毛细血管样结构的形成几乎没有影响,对内皮细胞的增殖也没有影响。我们还研究了人肿瘤坏死因子(TNF)-α对毛细血管样结构形成和内皮细胞增殖的影响。人TNF-α在浓度为100 U/ml时抑制C6胶质瘤细胞诱导的毛细血管样结构的形成,在浓度为1000 U/ml时抑制内皮细胞的增殖。这些结果表明,血管生成的诱导因胶质瘤细胞系而异,且血管生成与内皮细胞的增殖并不对应。TNF-α在体外可抑制胶质瘤中的血管生成。

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