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培养的牛犊垂体前叶细胞生长因子活性的产生。

Production of growth factor activity by cultured bovine calf anterior pituitary cells.

作者信息

Kudlow J E, Gerrie B M

出版信息

Endocrinology. 1983 Jul;113(1):104-10. doi: 10.1210/endo-113-1-104.

Abstract

Primary cultures of bovine calf anterior pituitary cells were observed to proliferate for at least eight doublings in a serum-free defined medium without the addition of mitogens or hormones. Insulin caused minor increments both in the rate of proliferation of cells from a doubling time of 31 h to 26 h and in the saturation density from 1 X 10(5) to 1.4 X 10(5) cells/cm2. To determine whether the pituitary cells could secrete a growth factor, medium conditioned by the pituitary cells was tested for mitogenic activity. Conditioned medium caused a dose-dependent increase in 3T3 fibroblast DNA synthesis indicating that it contained the equivalent mitogenic activity of either 2.5 X 10(-9) M epidermal growth factor (EGF) or 250 ng/ml fibroblast growth factor (FGF). 3T3 cell proliferation was also stimulated to a greater extent by conditioned medium than by EGF or FGF. Y1 adrenal cortical tumor cells were also stimulated by conditioned medium to synthesize DNA and proliferate. The mitogenic activity in the conditioned medium was heat and acid stable unlike pituitary FGF. No EGF could be detected in the conditioned medium by a RIA using antimouse EGF serum and a RIA for multiplication-stimulating activity was also negative. None of the classical pituitary hormones were mitogenic under the test conditions indicating that the mitogenic activity could not be attributed to the known pituitary hormones. Although these results indicate that pituitary cells secrete a growth factor(s), its identity is not established.

摘要

牛犊垂体前叶细胞的原代培养物在无血清限定培养基中,不添加促细胞分裂剂或激素的情况下,被观察到至少增殖了八次。胰岛素使细胞增殖速率从31小时的倍增时间略有增加至26小时,饱和密度从1×10⁵个细胞/cm²增加到1.4×10⁵个细胞/cm²。为了确定垂体细胞是否能分泌生长因子,检测了垂体细胞条件培养基的促有丝分裂活性。条件培养基导致3T3成纤维细胞DNA合成呈剂量依赖性增加,表明其含有相当于2.5×10⁻⁹M表皮生长因子(EGF)或250ng/ml成纤维细胞生长因子(FGF)的促有丝分裂活性。条件培养基对3T3细胞增殖的刺激程度也大于EGF或FGF。Y1肾上腺皮质肿瘤细胞也受到条件培养基的刺激而合成DNA并增殖。与垂体FGF不同,条件培养基中的促有丝分裂活性对热和酸稳定。使用抗小鼠EGF血清的放射免疫分析在条件培养基中未检测到EGF,且用于增殖刺激活性的放射免疫分析也为阴性。在测试条件下,没有一种经典的垂体激素具有促有丝分裂活性,这表明促有丝分裂活性不能归因于已知的垂体激素。尽管这些结果表明垂体细胞分泌一种或多种生长因子,但其身份尚未确定。

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