Chang A Y, Wyse B M
Biochim Biophys Acta. 1981 Feb 5;672(3):239-47. doi: 10.1016/0304-4165(81)90290-7.
An epithelial cell line, designated CHK-ACE, was established from the kidney of a spontaneously diabetic Chinese hamster from the highly inbred AC line. CHK-ACE was separated into two sublines, CHK-ACE-100 and CHK-ACE-400, by successive passages in 100 and 400 mg/dl glucose respectively. Extra- and intracellular activities of N-acetyl-beta-D-glucosaminidase and beta-D-galactosidase were measured in these cultures after exposure to varying concentrations of glucose (100, 200, 300 and 400 mg/dl) for one passage and 10% heated fetal calf serum for 6.5 h before enzyme measurements were taken; no apparent dependence on medium-glucose concentration was found. In serum-free medium, the time-dependent release of both N-acetyl-beta-D-glucosaminidase and beta-D-galactosidase was sustained for up to 24 h; no significant difference in their activities was found between CHK-ACE-100 cultures grown in 100 and 400 mg/dl glucose for one passage.
一种上皮细胞系,命名为CHK-ACE,是从高度近交AC系的一只自发性糖尿病中国仓鼠的肾脏中建立的。通过分别在100mg/dl和400mg/dl葡萄糖中连续传代,CHK-ACE被分离成两个亚系,CHK-ACE-100和CHK-ACE-400。在这些培养物中,在酶测量前,将其暴露于不同浓度的葡萄糖(100、200、300和400mg/dl)中传代一次,并在10%热灭活胎牛血清中培养6.5小时后,测量N-乙酰-β-D-氨基葡萄糖苷酶和β-D-半乳糖苷酶的细胞外和细胞内活性;未发现对培养基葡萄糖浓度有明显依赖性。在无血清培养基中,N-乙酰-β-D-氨基葡萄糖苷酶和β-D-半乳糖苷酶的时间依赖性释放可持续长达24小时;在100mg/dl和400mg/dl葡萄糖中传代一次培养的CHK-ACE-100培养物之间,它们的活性没有显著差异。