Pattillo R A, Hussa R O, Ruckert A C, Kurtz J W, Cade J M, Rinke M L
Endocrinology. 1979 Oct;105(4):967-74. doi: 10.1210/endo-105-4-967.
Gel filtration and radioimmunological studies were used to demonstrate that BeWo malignant trophoblastic cells, subcultured for more than 12 yr as roller tube colonies using dissection by scalpel, retained the ability to secrete large quantities of intact hCG. By contrast, BeWo cells that had been subcultured weekly for 12 hr using proteolytic enzyme dispersion lost their ability to secrete intact hCG. Rather, a large form of hCG-alpha was the major secretory product, along with lesser amounts of heterogeneous low molecular weight forms of hCG-beta. The gradual loss of hormone secretory ability and fidelity of hormone product by cells in continuous culture is a well known phenomenon. Our results suggest that the habitual use of trypsin-EDTA to subculture cells may accelerate this process.
采用凝胶过滤和放射免疫研究方法来证明,作为手术刀切割的滚管集落进行传代培养超过12年的BeWo恶性滋养层细胞,仍保留分泌大量完整人绒毛膜促性腺激素(hCG)的能力。相比之下,使用蛋白水解酶分散法每周传代培养12小时的BeWo细胞失去了分泌完整hCG的能力。相反,一种大分子形式的hCG-α是主要分泌产物,同时还有少量异质性低分子量形式的hCG-β。连续培养的细胞中激素分泌能力的逐渐丧失以及激素产物的保真度是一个众所周知的现象。我们的结果表明,习惯性地使用胰蛋白酶-乙二胺四乙酸(EDTA)进行细胞传代培养可能会加速这一过程。