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重组脱氧核糖核酸衍生的牛生长激素对维持在无胸腺裸鼠体内的牛乳腺组织α-乳白蛋白产生的影响。

Influence of recombinant deoxyribonucleic acid-derived bovine growth hormone on alpha-lactalbumin production by bovine mammary tissue maintained in athymic nude mice.

作者信息

Sheffield L G, Eppler C M, Tucker H A, Welsch C W

机构信息

Department of Dairy Science, University of Wisconsin, Madison 53706.

出版信息

J Dairy Sci. 1988 Jan;71(1):68-74. doi: 10.3168/jds.S0022-0302(88)79526-0.

Abstract

Mammary tissue from five cows was cut into pieces approximately 3 mm2 x .2 mm and placed subcutaneously in athymic mice (10 to 12 pieces/mouse). After 30 d, all mice were injected for 10 d with 17 beta-estradiol (1 microgram), progesterone (1 mg), ovine prolactin (1 mg), and growth hormone (recombinant DNA-derived bovine) (1 mg). Four grafts were then removed from each mouse, mice were ovariectomized, and subsequently mice were injected daily for 7 d with hydrocortisone (.2 mg, all mice), growth hormone (0, .25, .5, or 1.0 mg), and 0 or .5 mg ovine prolactin (three mice/treatment per udder). alpha-Lactalbumin content of grafts was 36 +/- 9 micrograms/mg DNA after treatment with estradiol, progesterone, growth hormone, and prolactin but before hydrocortisone, prolactin, and growth hormone treatment. Hydrocortisone treatment increased alpha-lactalbumin to 147 micrograms/mg DNA. Growth hormone plus hydrocortisone treatment increased alpha-lactalbumin to 391, 451, and 480 micrograms/mg DNA for .25, .5, and 1.0 mg/d of growth hormone, respectively. Prolactin plus hydrocortisone treatment increased alpha-lactalbumin to 466 micrograms/mg DNA. With exogenous prolactin, growth hormone increased alpha-lactalbumin content of grafts to 581, 647, and 689 micrograms/mg DNA for .25, .5, and 1.0 mg/d of growth hormone, respectively. Histological examination of tissues indicated that the effect of growth hormone was not mediated through increased epithelial area. Data suggest that bovine mammary tissue is capable of organotypic differentiation in athymic mice.

摘要

将五头奶牛的乳腺组织切成约3平方毫米×0.2毫米的小块,皮下植入无胸腺小鼠体内(每只小鼠植入10至12块)。30天后,所有小鼠连续10天注射17β-雌二醇(1微克)、孕酮(1毫克)、羊催乳素(1毫克)和生长激素(重组DNA来源的牛生长激素)(1毫克)。然后从每只小鼠身上取出4个移植物,对小鼠进行卵巢切除,随后连续7天每天给小鼠注射氢化可的松(0.2毫克,所有小鼠)、生长激素(0、0.25、0.5或1.0毫克),以及0或0.5毫克羊催乳素(每个乳房每处理三只小鼠)。在用雌二醇、孕酮、生长激素和催乳素处理后,但在氢化可的松、催乳素和生长激素处理前,移植物的α-乳白蛋白含量为36±9微克/毫克DNA。氢化可的松处理使α-乳白蛋白增加到147微克/毫克DNA。生长激素加氢化可的松处理使α-乳白蛋白分别增加到391、451和480微克/毫克DNA,生长激素剂量分别为0.25、0.5和1.0毫克/天。催乳素加氢化可的松处理使α-乳白蛋白增加到466微克/毫克DNA。在外源催乳素存在的情况下,生长激素使移植物的α-乳白蛋白含量分别增加到581、647和689微克/毫克DNA,生长激素剂量分别为0.25、0.5和1.0毫克/天。组织学检查表明,生长激素的作用不是通过增加上皮面积介导的。数据表明,牛乳腺组织在无胸腺小鼠中能够进行器官样分化。

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