Kanzaki T, Eto H, Umezawa A, Maeda T, Iwase H, Ito M
Cancer Res. 1981 Jun;41(6):2468-75.
A cell line of a benign tumor, trichilemmoma, was established in vitro and has been maintained in culture for 1.5 years with more than 30 passages. Plating efficiency was less than 0.1%, and population doubling time was 10 days. Saturation density was 10(5) cells/sq cm at the time of a monolayer with 98% cell viability. Ultrastructurally, tissue-cultured trichilemmoma cells showed desmosome-tonofilament complexes at cell-to-cell junctions. The tissue-cultured cells synthesized abundant glycogen (50 to 100 microgram/10(6) cells) e was 10 days. Saturation density was 10(5) cells/sq cm at the time of a monolayer with 98% cell viability. Ultrastructurally, tissue-cultured trichilemmoma cells showed desmosome-tonofilament complexes at cell-to-cell junctions. The tissue-cultured cells synthesized abundant glycogen (50 to 100 microgram/10(6) cells) e was 10 days. Saturation density was 10(5) cells/sq cm at the time of a monolayer with 98% cell viability. Ultrastructurally, tissue-cultured trichilemmoma cells showed desmosome-tonofilament complexes at cell-to-cell junctions. The tissue-cultured cells synthesized abundant glycogen (50 to 100 microgram/10(6) cells) as observed in vivo. Gas chromatographic analysis revealed that extracted glycogen was composed of glucose alone. Chromosome analyses with trypsin-Giemsa banding showed an abnormal karyotype with hypodiploid modal numbers of 44 and 45. There were four marker chromosomes observed in 100% of cells in 100 metaphase cells examined. Cells did not grow on fibroblast monolayers or in soft agar in vitro but did induce tumors in athymic nude mice (12 of 15) after the s.c. injection of tissue-cultured cells (2.5 x 10(6) to 4.5 x 10(7) cells/mouse). The histological characteristics of the tumors in nude mice were similar to those of the original tumor. This is the first time, to our knowledge, that a benign human tumor cell line has been established in vitro which can induce tumors in nude mice.
一种良性肿瘤毛鞘瘤的细胞系在体外建立,并已在培养中维持了1.5年,传代超过30次。接种效率低于0.1%,群体倍增时间为10天。单层时的饱和密度为10(5)个细胞/平方厘米,细胞活力为98%。超微结构上,组织培养的毛鞘瘤细胞在细胞间连接处显示桥粒-张力丝复合体。组织培养的细胞合成了大量糖原(50至100微克/10(6)个细胞),与体内观察到的情况一样。气相色谱分析表明,提取的糖原仅由葡萄糖组成。用胰蛋白酶-吉姆萨显带进行的染色体分析显示核型异常,亚二倍体众数为44和45。在检查的100个中期细胞中,100%的细胞观察到有四条标记染色体。细胞在体外不能在成纤维细胞单层上生长或在软琼脂中生长,但在皮下注射组织培养细胞(2.5×10(6)至4.5×1×(7)个细胞/小鼠)后能在无胸腺裸鼠中诱导肿瘤(15只中有12只)。裸鼠体内肿瘤的组织学特征与原发肿瘤相似。据我们所知,这是首次在体外建立能在裸鼠中诱导肿瘤的良性人类肿瘤细胞系。