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[大鼠胶质瘤细胞体外诱导血管生成]

[Angiogenesis induced by rat glioma cells in vitro].

作者信息

Niida H, Minakawa T, Tanaka R

机构信息

Department of Neurosurgery, Niigata University, Japan.

出版信息

No Shinkei Geka. 1992 Nov;20(11):1169-72.

PMID:1280347
Abstract

Angiogenesis induced by rat glioma cells was examined in vitro using a double chamber co-culture system. Cultured microvascular endothelial cells from Fisher 344 rat brain, rat C6 glioma cells and rat T9 gliosarcoma cells were used for this study. Endothelial cells, cultured on type I collagen, formed capillary-like structures. In the co-culture system, C6 glioma cells promoted this formation. On the other hand T9 gliosarcoma cells had no effect on it. The supernatants of C6 glioma cells and T9 gliosarcoma cells suppressed the proliferation of the endothelial cells. C6 glioma cells probably produce and release soluble factors promoting angiogenesis. The proliferation of endothelial cells is thus suppressed while angiogenesis is made more intense. This in-vitro model is useful to elucidate the mechanism of tumor angiogenesis and to evaluate the promoting and inhibiting factors of angiogenesis.

摘要

采用双室共培养系统在体外检测大鼠胶质瘤细胞诱导的血管生成。本研究使用了从Fisher 344大鼠脑分离培养的微血管内皮细胞、大鼠C6胶质瘤细胞和大鼠T9胶质肉瘤细胞。在I型胶原上培养的内皮细胞形成了毛细血管样结构。在共培养系统中,C6胶质瘤细胞促进了这种结构的形成。另一方面,T9胶质肉瘤细胞对其没有影响。C6胶质瘤细胞和T9胶质肉瘤细胞的上清液抑制了内皮细胞的增殖。C6胶质瘤细胞可能产生并释放促进血管生成的可溶性因子。因此,在内皮细胞增殖受到抑制的同时,血管生成却更加活跃。这个体外模型有助于阐明肿瘤血管生成的机制,并评估血管生成的促进和抑制因子。

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