Wu Y, Ackerman J L, Strawich E S, Rey C, Kim H-M, Glimcher M J
Laboratory for the Study of Skeletal Disorders and Rehabilitation, Department of Orthopaedic Surgery, Children's Hospital, Harvard Medical School, Boston, MA 02115, USA.
Calcif Tissue Int. 2003 May;72(5):610-26. doi: 10.1007/s00223-002-1068-8. Epub 2003 May 6.
Previous 31P cross-polarization and differential cross-polarization magic angle spinning (CP/MAS and DCP/MAS) solid-state NMR spectroscopy studies of native bone and of the isolated crystals of the calcified matrix synthesized by osteoblasts in cell culture identified and characterized the major PO(-3)(4) phosphate components of the mineral phase. The isotropic and anisotropic chemical shift parameters of the minor HPO(-2)(4) component in bone mineral and in mineral deposited in osteoblast cell cultures were found to differ significantly from those of brushite, octacalcium phosphate, and other synthetic calcium phosphates. However, because of in vivo and in vitro evidence that phosphoproteins may play a significant role in the nucleation of the solid mineral phase of calcium phosphate in bone and other vertebrate calcified tissues, the focus of the current solid-state 31P NMR experiments was to detect the possible presence of and characterize the phosphoryl groups of phosphoproteins in bone at the very earliest stages of bone mineralization, as well as the possible presence of calcium-phosphoprotein complexes. The present study demonstrates that by far the major phosphate components identified by solid-state 31P NMR in the very earliest stages of mineralization are protein phosphoryl groups which are not complexed with calcium. However, very small amounts of calcium-complexed protein phosphoryl groups as well as even smaller, trace amounts of apatite crystals were also present at the earliest phases of mineralization. These data support the hypothesis that phosphoproteins complexed with calcium play a significant role in the initiation of bone calcification.
以往利用31P交叉极化和差示交叉极化魔角旋转(CP/MAS和DCP/MAS)固态核磁共振波谱技术对天然骨以及在细胞培养中由成骨细胞合成的钙化基质分离晶体进行的研究,确定并表征了矿相中的主要PO₄³⁻磷酸成分。结果发现,骨矿物质以及成骨细胞培养物中沉积矿物质中的次要HPO₄²⁻成分的各向同性和各向异性化学位移参数,与透钙磷石、磷酸八钙和其他合成磷酸钙的化学位移参数有显著差异。然而,鉴于体内和体外证据均表明磷蛋白可能在骨和其他脊椎动物钙化组织中磷酸钙固体矿相的成核过程中发挥重要作用,当前固态³¹P核磁共振实验的重点是检测骨矿化最早期阶段磷蛋白的磷酸基团是否可能存在并对其进行表征,以及是否可能存在钙 - 磷蛋白复合物。本研究表明,在矿化最早阶段通过固态³¹P核磁共振鉴定出的主要磷酸盐成分是未与钙结合的蛋白质磷酸基团。然而,在矿化的最早阶段也存在极少量与钙结合的蛋白质磷酸基团以及甚至更少的痕量磷灰石晶体。这些数据支持了与钙结合的磷蛋白在骨钙化起始过程中起重要作用这一假说。