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在胶原凝胶内无血清培养的小鼠乳腺上皮细胞的体外转化

In vitro transformation of mouse mammary epithelial cells grown serum-free inside collagen gels.

作者信息

Guzman R C, Osborn R C, Bartley J C, Imagawa W, Asch B B, Nandi S

出版信息

Cancer Res. 1987 Jan 1;47(1):275-80.

PMID:3098407
Abstract

Mammary epithelial cells from 4-month-old virgin BALB/c mice were cultured inside collagen gels in the following serum-free media: Dulbecco's modified Eagle's medium:Hams's F-12 (1:1) supplemented with: insulin (10 micrograms/ml), bovine serum albumin (5 mg/ml), and epidermal growth factor (5 ng/ml); insulin, bovine serum albumin, progesterone (0.05 microgram/ml), and prolactin (1 microgram/ml); insulin, bovine serum albumin, progesterone, prolactin, and linoleic acid (10 micrograms/ml). Cells proliferated in all these media. The cells were treated with 0.01 micrograms/ml of 7,12-dimethylbenz(a)anthracene or 100 micrograms/ml of N-nitroso-N-methylurea on day 3 of culture and, subsequently, at 1-week intervals for 3-6 weeks. Tetradecanoylphorbol acetate (0.1 micrograms/ml) was added to selected cultures. The cultures were maintained for up to 9 weeks; the cells were then removed from the collagen gels, placed in monolayer culture for 2 days, and removed from monolayer culture, and 5 X 10(5) cells were transplanted to each of the gland-free mammary fat pads of 3-week-old female mice. Approximately 10 weeks after transplantation, the transplanted mammary fat pads were examined for outgrowths. Cells that were not treated with carcinogen and cultured for up to 9 weeks in different serum-free media and transplanted to the gland-free mammary fat pad produced only ductal outgrowths similar in morphology to the ducts of the virgin host's mammary glands. Six treatments with 7,12-dimethylbenz(a)anthracene, of cells grown in the presence of epidermal growth factor, induced 31% spindle cell tumors, 17% ductal hyperplasias, and 5% lobuloalveolar hyperplasias. Cells that were grown in epidermal growth factor and treated three times with N-nitroso-N-methylurea produced 23% ductal hyperplasias and 17% lobuloalveolar hyperplasias. Cells grown in the presence of progesterone and prolactin and treated three times with 7,12-dimethylbenz(a)anthracene produced up to 23% lobuloalveolar hyperplasias and 12% ductal hyperplasias. Three treatments with N-nitroso-N-methylurea of cells grown in progesterone- and prolactin-containing media produced a maximum of 50% lobuloalveolar hyperplasias and 33% ductal hyperplasias. The lobuloalveolar hyperplasias have the characteristics of the precancerous hyperplastic alveolar nodules found in mouse mammary tumorigenesis. The in vitro carcinogen-induced lobuloalveolar hyperplasias were transplantable, maintained their lobuloalveolar morphology in virgin hosts, and produced carcinomas.

摘要

取自4月龄处女BALB/c小鼠的乳腺上皮细胞在以下无血清培养基中培养于胶原凝胶内:杜尔贝科改良伊格尔培养基:哈姆氏F-12(1:1),添加:胰岛素(10微克/毫升)、牛血清白蛋白(5毫克/毫升)和表皮生长因子(5纳克/毫升);胰岛素、牛血清白蛋白、孕酮(0.05微克/毫升)和催乳素(1微克/毫升);胰岛素、牛血清白蛋白、孕酮、催乳素和亚油酸(10微克/毫升)。细胞在所有这些培养基中均有增殖。在培养第3天,用0.01微克/毫升的7,12-二甲基苯并(a)蒽或100微克/毫升的N-亚硝基-N-甲基脲处理细胞,随后每隔1周处理一次,持续3 - 6周。向选定培养物中添加十四酰佛波醇乙酸酯(0.1微克/毫升)。培养物维持长达9周;然后将细胞从胶原凝胶中取出,置于单层培养2天,再从单层培养中取出,将5×10⁵个细胞移植到3周龄雌性小鼠的每个无腺乳腺脂肪垫中。移植后约10周,检查移植的乳腺脂肪垫有无增生。未用致癌物处理且在不同无血清培养基中培养长达9周并移植到无腺乳腺脂肪垫的细胞仅产生形态与处女宿主乳腺导管相似的导管增生。在表皮生长因子存在下生长的细胞经6次7,12-二甲基苯并(a)蒽处理后,诱导出31%的梭形细胞瘤、17%的导管增生和5%的小叶腺泡增生。在表皮生长因子存在下生长且经3次N-亚硝基-N-甲基脲处理的细胞产生23%的导管增生和17%的小叶腺泡增生。在孕酮和催乳素存在下生长且经3次7,12-二甲基苯并(a)蒽处理的细胞产生高达23%的小叶腺泡增生和12%的导管增生。在含孕酮和催乳素的培养基中生长的细胞经3次N-亚硝基-N-甲基脲处理后,最多产生50%的小叶腺泡增生和33%的导管增生。小叶腺泡增生具有小鼠乳腺肿瘤发生过程中癌前增生性肺泡结节的特征。体外致癌物诱导的小叶腺泡增生可移植,在处女宿主中保持其小叶腺泡形态,并产生癌。

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