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[一种新的人肾癌细胞系(TC-1)的建立及其白细胞介素-6(IL-6)的产生]

[Establishment of a new human renal cancer cell line (TC-1) and its productivity of interleukin-6 (IL-6)].

作者信息

Muraki J, Nakazano M

机构信息

Department of Urology, Tochigi Cancer Center, Japan.

出版信息

Nihon Hinyokika Gakkai Zasshi. 1992 Nov;83(11):1882-9. doi: 10.5980/jpnjurol1989.83.1882.

Abstract

We established a new cell line (TC-1) from primary site of a renal cell carcinoma (RCC) patient. Its doubling time in tissue culture was 20 hours at 45th passage and mycoplasma contamination test was negative. The karyotypic analysis demonstrated a human karyotype with a modal number of 70. A consistent chromosomal abnormality was noted such as No. 4 monosomy, No. 7 trisomy and a loss of Y chromosome. Electron microscopic examination showed a brush border, vacuoles and abundant glycogen granules in the cytoplasm, which was compatible with RCC cells. This cell line was transplantable to nude mice and the grown tumor closely resembled the original tumor, i.e. clear cell type and hypervascularity. High titer of interleukin-6 (IL-6) was detected in the supernatant of TC-1 cell culture (approximately 5 ng/ml) as well as in sera of nude mice bearing this tumor (260 pg/ml). Exogenous IL-6 did not enhance the TC-1 cell proliferation as determined by cell count. Flow cytometric analysis could not demonstrate the existence of IL-6 receptor on the cell surface. These results suggested the produced IL-6 did not act as an autocrine growth factor in the cell line. Additional IL-1 alpha to the culture medium induced 3-4 times higher concentration of IL-6 in the culture supernatant compared with that of non-stimulating cells, while exogenous TNF alpha did not stimulate IL-6 production.

摘要

我们从一名肾细胞癌(RCC)患者的原发部位建立了一种新的细胞系(TC-1)。其在组织培养中的倍增时间在第45代时为20小时,支原体污染检测为阴性。核型分析显示为人类核型,众数为70。观察到一致的染色体异常,如4号染色体单体、7号染色体三体以及Y染色体缺失。电子显微镜检查显示细胞质中有刷状缘、空泡和丰富的糖原颗粒,这与肾癌细胞相符。该细胞系可移植到裸鼠体内,生长的肿瘤与原发肿瘤非常相似,即透明细胞型和血管丰富。在TC-1细胞培养上清液(约5 ng/ml)以及携带该肿瘤的裸鼠血清(260 pg/ml)中检测到高滴度的白细胞介素-6(IL-6)。通过细胞计数确定,外源性IL-6并未增强TC-1细胞的增殖。流式细胞术分析未在细胞表面证实IL-6受体的存在。这些结果表明,所产生的IL-6在该细胞系中并非作为自分泌生长因子起作用。与未刺激的细胞相比,向培养基中添加额外的IL-1α可使培养上清液中IL-6的浓度升高3 - 4倍,而外源性TNFα并未刺激IL-6的产生。

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