Sorimachi K
Department of Microbiology, Dokkyo University School of Medicine, Tochigi, Japan.
Cell Biochem Funct. 1988 Jan;6(1):25-9. doi: 10.1002/cbf.290060105.
Human urinary bladder carcinoma cells (JTC-32) retain a low alkaline phosphatase activity. Prednisolone or a hypertonic concentration of NaCl caused a moderate increase in the activity (10- to 15-fold of control), but dibutyryl cAMP or butyrate did not. Examination of the combined effect of these four agents revealed that they acted synergistically in any combination. When the cells were incubated with the four agents together, the enzyme activity increased 60- to 250-fold. Serum also contributed to this synergistic increase. These agents slightly inhibited cell growth and protein synthesis. The enzyme induction was completely inhibited by cycloheximide or actinomycin D. The synergistic effect of the four agents on the enzyme activity was also observed in other strains of carcinoma cells, human urinary bladder carcinoma cells (JTC-30) and monkey hepatocarcinoma cells (NCLP-6E). Thus, it is concluded that the coexistence of the four agents provides general and superior conditions for the induction of alkaline phosphatase in cultured carcinoma cells.
人膀胱癌细胞(JTC - 32)的碱性磷酸酶活性较低。泼尼松龙或高渗浓度的氯化钠可使该活性适度增加(为对照的10至15倍),但二丁酰环磷腺苷或丁酸盐则无此作用。对这四种试剂联合作用的检测表明,它们以任何组合方式作用时均具有协同效应。当细胞与这四种试剂一起孵育时,酶活性增加了60至250倍。血清也促成了这种协同性增加。这些试剂对细胞生长和蛋白质合成有轻微抑制作用。环己酰亚胺或放线菌素D可完全抑制酶的诱导。在其他癌细胞株,即人膀胱癌细胞(JTC - 30)和猴肝癌细胞(NCLP - 6E)中也观察到了这四种试剂对酶活性的协同作用。因此,可以得出结论,这四种试剂的共同存在为培养的癌细胞中碱性磷酸酶的诱导提供了普遍且优越的条件。