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一种检测由培养的人肿瘤细胞衍生的生长因子对几种类型牛内皮细胞刺激作用的分析方法。

An assay measuring the stimulation of several types of bovine endothelial cells by growth factor(s) derived from cultured human tumor cells.

作者信息

Olander J V, Marasa J C, Kimes R C, Johnston G M, Feder J

出版信息

In Vitro. 1982 Feb;18(2):99-107. doi: 10.1007/BF02796401.

Abstract

Endothelial cell growth factor(s) from several previously untested human tumor cell lines (i.e., SK-HEP-1, MG63, A375, TE671-C1, RD) were detected using a low cell inoculum growth assay. The final cell density in the 2-cm2 wells was determined by a highly sensitive DNA content measurement performed directly in the tissue culture plates. The sensitivity of the assay to human tumor cell growth factors depended critically on the low cell inocula, 2,000 to 5,000 cells/well. Most of the bovine endothelial cells used were cloned from primary cultures; all the cell lines obtained from various fetal and nonfetal sources responded to the growth factor(s) (up to a 16x stimulation) as well as to endothelial cell growth supplement. Dose response curves showing the cell specific response of bovine endothelial cells were obtained. The growth stimulatory activity and the in vivo chick embryo chorioallantoic membrane assay responses correlated sufficiently to imply that the assay is detecting tumor angiogenesis factor or some closely related activity. This in vitro assay should prove useful in the identification and purification of tumor-derived factors and in the elucidation of the role of these factors in the events comprising angiogenesis.

摘要

使用低细胞接种量生长测定法检测了几种先前未经测试的人类肿瘤细胞系(即SK-HEP-1、MG63、A375、TE671-C1、RD)中的内皮细胞生长因子。通过直接在组织培养板中进行的高灵敏度DNA含量测量来确定2平方厘米孔中的最终细胞密度。该测定法对人类肿瘤细胞生长因子的敏感性主要取决于低细胞接种量,即每孔2000至5000个细胞。所用的大多数牛内皮细胞是从原代培养物中克隆出来的;从各种胎儿和非胎儿来源获得的所有细胞系对生长因子(刺激倍数高达16倍)以及内皮细胞生长补充剂均有反应。获得了显示牛内皮细胞细胞特异性反应的剂量反应曲线。生长刺激活性与体内鸡胚绒毛尿囊膜测定反应充分相关,这意味着该测定法正在检测肿瘤血管生成因子或某些密切相关的活性。这种体外测定法在鉴定和纯化肿瘤衍生因子以及阐明这些因子在血管生成事件中的作用方面应会证明是有用的。

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