Kimura G, Sugisaki Y, Masugi Y, Nakazawa N
Department of Pathology, Nippon Medical School, Tokyo, Japan.
Urol Int. 1992;48(1):25-30. doi: 10.1159/000282291.
A medium that had been conditioned by PC-3 cells stimulated the calcification of a human osteoblastic cell line, Tak-10, in a nonmitogenic culture. The calcification of the osteoblasts was stimulated maximally at a 25% concentration of the conditioned medium. Calcification activity was markedly enhanced by the addition of both prostatic acid phosphatase (PAP) and its substrate, alpha-glycerophosphate, to the medium; however, PAP added alone did not enhance this activity. These results suggest that human prostatic carcinoma cells produce a factor that stimulates the calcification of the human osteoblasts. Results have also suggested that PAP is a requisite for osteogenesis provided that its substrates are abundant in the medium.
经PC - 3细胞条件培养的培养基在非促有丝分裂培养中刺激了人成骨细胞系Tak - 10的钙化。在条件培养基浓度为25%时,成骨细胞的钙化受到最大刺激。向培养基中添加前列腺酸性磷酸酶(PAP)及其底物α - 甘油磷酸后,钙化活性显著增强;然而,单独添加PAP并没有增强这种活性。这些结果表明,人前列腺癌细胞产生一种刺激人成骨细胞钙化的因子。结果还表明,只要培养基中PAP的底物充足,PAP就是骨生成所必需的。