Ali N N, Rowe J, Teich N M
Laboratory of Viral-mediated Cell Differentiation, Imperial Cancer Research Fund, London, England, United Kingdom.
J Bone Miner Res. 1996 Apr;11(4):512-20. doi: 10.1002/jbmr.5650110412.
Alkaline phosphatase (ALP) plays an important role in bone mineralization; high levels in differentiated osteoblasts allows their identification easily in vitro. It is generally assumed that the activity of ALP in osteosarcoma-derived cell lines commonly used in studies of bone cell biology is exclusively due to the bone/liver/kidney (BLK) isoenzyme. However, we noted that two human osteosarcoma cell lines, U-2 OS and U-393 OS, predominantly expressed a truncated 1.8 kb mRNA for BLK-ALP. This observation stimulated further investigation upon the ability of ALP to form functional protein. We found that, unlike the BLK-ALP of the Saos-2 osteosarcoma cell line, the activity of U-2 OS ALP was thermostable, unaffected by L-homoarginine and levamisole, but inhibited by L-phenylalanine; these properties are characteristic of the placental and/or placental-like (PL-/PL-like ALP) isoenzymes which are 98% homologous at the amino acid level. In the U-393 OS cell line, which expresses the normal-sized 2.5 kb mRNA in substantially higher levels than that produced by U-2 OS cells, the ALP activity had kinetic properties very similar to that produced by the Saos-2 line for all criteria tested. The HOS osteosarcoma cell line (also known as TE-85), which express the normal-sized 2.5 kb BLK-ALP mRNA only, exhibited ALP activity with kinetic properties of both the BLK and PL-/PL-like isoenzymes. The three test lines, U-2 OS, U-393 OS and HOS, produced PL-/PL-like ALP mRNA and protein constitutively, and levels of these increased in cells treated with 1 microM dexamethasone. However, dexamethasone treatment of cells did not alter the types of ALP isoenzyme expressed. Thus our results show that, like Saos-2 cells, U-393 OS cells produce active BLK-ALP exclusively, whereas U-2 OS cells produce PL-/PL-like ALP only, and the HOS cell line produces both. Our findings have important implications for phenotypic characterization of various human osteosarcoma cell lines, and suggest that the production of PL-/PL-like ALP may be a more common occurrence in osteosarcomas than was originally thought.
碱性磷酸酶(ALP)在骨矿化过程中发挥着重要作用;分化的成骨细胞中高水平的碱性磷酸酶使得在体外易于识别它们。一般认为,在骨细胞生物学研究中常用的骨肉瘤衍生细胞系中,ALP的活性完全归因于骨/肝/肾(BLK)同工酶。然而,我们注意到两个人骨肉瘤细胞系U-2 OS和U-393 OS主要表达截短的1.8 kb BLK-ALP mRNA。这一观察结果促使我们进一步研究ALP形成功能蛋白的能力。我们发现,与Saos-2骨肉瘤细胞系的BLK-ALP不同,U-2 OS ALP的活性具有热稳定性,不受L-高精氨酸和左旋咪唑的影响,但受L-苯丙氨酸抑制;这些特性是胎盘和/或胎盘样(PL-/PL样ALP)同工酶的特征,它们在氨基酸水平上有98%的同源性。在U-393 OS细胞系中,其表达的正常大小的2.5 kb mRNA水平明显高于U-2 OS细胞产生的水平,对于所有测试标准,ALP活性的动力学特性与Saos-2细胞系产生的非常相似。HOS骨肉瘤细胞系(也称为TE-85)仅表达正常大小的2.5 kb BLK-ALP mRNA,其ALP活性表现出BLK和PL-/PL样同工酶的动力学特性。三个测试细胞系U-2 OS、U-393 OS和HOS持续产生PL-/PL样ALP mRNA和蛋白质,在用1 microM地塞米松处理的细胞中,这些物质的水平会升高。然而,地塞米松处理细胞并没有改变所表达的ALP同工酶类型。因此,我们的结果表明,与Saos-2细胞一样,U-393 OS细胞仅产生活性BLK-ALP,而U-2 OS细胞仅产生PL-/PL样ALP,HOS细胞系则同时产生这两种。我们的发现对于各种人骨肉瘤细胞系的表型特征具有重要意义,并表明PL-/PL样ALP的产生在骨肉瘤中可能比最初认为的更为常见。