Roach H I
Academic Orthopaedic Unit, Southampton University, General Hospital.
Cell Biol Int. 1994 Jun;18(6):617-28. doi: 10.1006/cbir.1994.1088.
Four major non-collagenous bone proteins were localised by single and double immuno- histochemistry during de novo mineralisation and bone resorption. Both osteopontin and bone sialoprotein were localised ahead of the mineralisation front, suggesting that both proteins are necessary for the initiation of bone mineralisation. This supports previous suggestions that bone sialoprotein acts as a crystal nucleator. The role of osteopontin is less certain, but might be related to ensuring that only the right type of crystal is formed. Osteocalcin and osteonectin were not present in areas of first crystal formation, but were present in the fully mineralised matrix. Their role may be to control the size and speed of crystal formation. Osteopontin, bone sialoproteins and osteocalcin (but not osteonectin) were also present at reversal lines. Interpreting this localisation together with information from the literature, the following functions are suggested during resorption: Osteocalcin may act as a chemoattractant for osteoclasts, while both osteopontin and bone sialoprotein may facilitate the binding of osteoclasts via the arg-gly-asp motif.
在新生矿化和骨吸收过程中,通过单免疫组织化学和双免疫组织化学对四种主要的非胶原蛋白进行了定位。骨桥蛋白和骨唾液蛋白均定位于矿化前沿之前,这表明这两种蛋白质对于骨矿化的起始都是必需的。这支持了先前关于骨唾液蛋白作为晶体成核剂的观点。骨桥蛋白的作用尚不太明确,但可能与确保仅形成正确类型的晶体有关。骨钙素和骨连接蛋白在最初晶体形成的区域中不存在,但存在于完全矿化的基质中。它们的作用可能是控制晶体形成的大小和速度。骨桥蛋白、骨唾液蛋白和骨钙素(但不包括骨连接蛋白)也存在于反转线处。结合文献信息对这种定位进行解读,在吸收过程中提出了以下功能:骨钙素可能作为破骨细胞的趋化因子,而骨桥蛋白和骨唾液蛋白都可能通过精氨酸-甘氨酸-天冬氨酸基序促进破骨细胞的结合。