Borisov A B, Bulychev A G
Tsitologiia. 1983 Apr;25(4):452-7.
Activities of lysosomal enzymes (acid phosphatase, N-acetyl-beta-D-glucosaminidase, acid lipase and cathepsin D) have been examined in a synchronized culture of mouse L-fibroblasts. Cell synchronization was achieved by the double thymidine block with a subsequent mitotic selection after colcemid treatment. Specific activities of the enzymes studied were found to be higher in S-G2 that in G1. There is a linear increase (approximate doubling) in enzyme activities per cell from G1 to M. Activity of galactosyltransferase, a marker of the Golgi apparatus, declined in mitotic cells in comparison with the interphase cells. Ultrastructural examination of L-cells revealed a reduction of the intracellular membrane system including the Golgi apparatus during mitosis. Changes in the Golgi apparatus activity have been considered as a possible regulatory point of lysosome formation. The data presented are compared with the results of morphological studies of lysosomal system in L-cells.
在小鼠L-成纤维细胞的同步培养物中检测了溶酶体酶(酸性磷酸酶、N-乙酰-β-D-氨基葡萄糖苷酶、酸性脂肪酶和组织蛋白酶D)的活性。通过双胸腺嘧啶核苷阻断并在秋水仙酰胺处理后进行后续的有丝分裂选择来实现细胞同步化。所研究的酶的比活性在S-G2期高于G1期。从G1期到M期,每个细胞的酶活性呈线性增加(约加倍)。与间期细胞相比,有丝分裂细胞中高尔基体标志物半乳糖基转移酶的活性下降。L细胞的超微结构检查显示,有丝分裂期间包括高尔基体在内的细胞内膜系统减少。高尔基体活性的变化被认为是溶酶体形成的一个可能调控点。将所呈现的数据与L细胞溶酶体系统的形态学研究结果进行了比较。