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Constitutive expression of non‐bone/liver/kidney alkaline phosphatase in human osteosarcoma cell lines
Author(s) -
Ali Nadire N.,
Rowe Janice,
Teich Natalie M.
Publication year - 1996
Publication title -
journal of bone and mineral research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.882
H-Index - 241
eISSN - 1523-4681
pISSN - 0884-0431
DOI - 10.1002/jbmr.5650110412
Subject(s) - alkaline phosphatase , cell culture , osteosarcoma , microbiology and biotechnology , isozyme , biology , messenger rna , osteoblast , chemistry , in vitro , enzyme , biochemistry , cancer research , gene , genetics
Abstract 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 osteosarcomaderived 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 expresses 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 μM 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.