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首页> 外文期刊>Journal of cell biology >Mitogenic activity of pituitary hormones on cell cultures of normal and carcinogen-induced tumor epithelium from rat mammary glands
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Mitogenic activity of pituitary hormones on cell cultures of normal and carcinogen-induced tumor epithelium from rat mammary glands

机译:垂体激素对正常和致癌物诱导的大鼠乳腺肿瘤上皮细胞培养的促分裂活性

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摘要

Cell suspension containing normal or tumor epithelium were readily obtained by enzymatically digesting rat mammary glands from perphenazine-treated (prolactin-hypersecreting) cycling, female virgin animals or hormone- responsive mammary tumors from animal treated with dimethylbenzanthracene. Cell suspensions were fractioned into predominantly epithelial and predominantly stromal cells by their differential rates of attachment to culture dishes. Both normal mammary and tumor epithelial cells were characterized by the presence of specific cell-junctional complexes, desmosome-like structures, surface microvilli, and their ability to synthesize casein. Serum-dependent protease activity was greater in cultures derived from tumors, and cells from such cultures grew in agarose whereas those from the non-neoplastic gland did not. The addition of prolactin to the culture medium stimulated DNA synthesis in primary or secondary epithelial cultures from tumors, whereas additional insulin and hydrocortisone with prolactin were required for similar levels of DNA synthesis in cultures from non-neoplastic glands. The fraction of cells synthesizing DNA was, however, smaller than that with 10 percent serum measured in the same time period. Both growth hormone and epidermal growth factor stimulated DNA synthesis but to a lesser extent than did prolactin. Prolactin with hydrocortisone and insulin were relatively inactive in promoting DNA synthesis of the nonepithelial cells whereas pituitary fibroblast growth factor was more active. These mitogenic effects were obtained when the hormones were added to the medium at near physiological concentrations, and paralleled the known activities of the hormones in control of mammary gland growth and development in the rat.
机译:通过酶促消化经奋乃静处理过的(催乳素分泌过多)自行车,雌性处女动物或经二甲基苯并蒽处理过的动物的激素反应性乳腺肿瘤,可以容易地获得含有正常或肿瘤上皮的细胞悬液。通过将细胞悬浮液与培养皿的附着速率不同,将其分为主要上皮细胞和主要基质细胞。正常的乳腺和肿瘤上皮细胞均以特定的细胞连接复合物,桥粒样结构,表面微绒毛及其合成酪蛋白的能力为特征。在源自肿瘤的培养物中,血清依赖性蛋白酶活性更高,并且来自此类培养物的细胞在琼脂糖中生长,而来自非肿瘤性腺的细胞则没有。向培养基中添加催乳素可刺激肿瘤的一级或继发上皮培养物中的DNA合成,而在非肿瘤性腺体中,DNA合成的相似水平需要额外的胰岛素和氢化可的松与催乳素。然而,合成DNA的细胞比例要小于同时期测定的10%血清的比例。生长激素和表皮生长因子均能刺激DNA合成,但程度要比催乳激素低。催乳素和氢化可的松和胰岛素在促进上皮细胞DNA合成方面相对无效,而垂体成纤维细胞生长因子则更活跃。当将激素以接近生理浓度的浓度添加到培养基中时,便获得了这些促有丝分裂作用,并与已知的激素在控制大鼠乳腺生长和发育中的活性相当。

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