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乙基亚硝基脲对培养上皮细胞的转化作用。I型前胶原链表达的改变。

Transformation of cultured epithelial cells by ethylnitrosourea. Altered expression of type I procollagen chains.

作者信息

Keski-Oja J, Alitalo K, Hautanen A, Rapp U R

出版信息

Biochim Biophys Acta. 1984 Mar 23;803(3):153-62. doi: 10.1016/0167-4889(84)90005-3.

Abstract

Cultured epithelial rodent cells were transformed in vitro using ethylnitrosourea as a carcinogen either alone or in combination with the tumor promoter 12-O-tetradecanoylphorbol-13-acetate (TPA). The frequency of transformation in the absence of TPA was 5 X 10(-4) at 10 micrograms/ml ethylnitrosourea. Growth of ethylnitrosourea-treated cells in TPA-substituted medium increased the transformation frequency 8-fold. Colonies of transformed cells were isolated from soft agar and analyzed for the production of pericellular matrix glycoproteins. The ethylnitrosourea-transformed cells retained pericellular matrix structures, typical of the nontransformed control cells. Parent cells produced into their culture media fibronectin and procollagen types I and III as their major pericellular glycoproteins. The ethylnitrosourea-transformed cells synthesized and secreted altered procollagen polypeptides. The procollagen of ethylnitrosourea-transformed cells apparently consisted mainly of homotrimeric pro alpha 1 molecules, with smaller amounts of basement membrane procollagen-like chains. Fibronectin synthesis or secretion was not affected by ethylnitrosourea-induced transformation, but the production of fibronectin was enhanced in the transformed cultures treated with TPA. Also, the deposition of procollagen and fibronectin into the pericellular matrix was not affected by ethylnitrosourea-transformation. Very similar changes had previously been observed in murine sarcoma virus-transformed cells. The change of procollagen type I thus appears to be a correlate of malignant transformation of cultured epithelial cells. The results indicate that ethylnitrosourea can induce malignant transformation of epithelial cells in culture and modify production and deposition of pericullular glycoproteins.

摘要

使用乙基亚硝基脲作为致癌物,单独或与肿瘤促进剂12-O-十四烷酰佛波醇-13-乙酸酯(TPA)联合,在体外对培养的啮齿动物上皮细胞进行转化。在不存在TPA的情况下,当乙基亚硝基脲浓度为10微克/毫升时,转化频率为5×10⁻⁴。在TPA替代培养基中培养经乙基亚硝基脲处理的细胞,使转化频率提高了8倍。从软琼脂中分离出转化细胞集落,并分析其细胞外基质糖蛋白的产生情况。经乙基亚硝基脲转化的细胞保留了非转化对照细胞典型的细胞外基质结构。亲本细胞在其培养基中产生纤连蛋白以及I型和III型前胶原作为其主要的细胞外糖蛋白。经乙基亚硝基脲转化的细胞合成并分泌改变的前胶原多肽。经乙基亚硝基脲转化的细胞的前胶原显然主要由同三聚体的前α1分子组成,还有少量基底膜前胶原样链。乙基亚硝基脲诱导的转化不影响纤连蛋白的合成或分泌,但在用TPA处理的转化培养物中纤连蛋白的产生增加。此外,前胶原和纤连蛋白在细胞外基质中的沉积不受乙基亚硝基脲转化的影响。此前在鼠肉瘤病毒转化的细胞中观察到非常相似的变化。因此,I型前胶原的变化似乎是培养的上皮细胞恶性转化的一个相关因素。结果表明,乙基亚硝基脲可诱导培养的上皮细胞发生恶性转化,并改变细胞外糖蛋白的产生和沉积。

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