Wang Chuanyi, Wang Yong, Huffman Nichole T, Cui Chaoying, Yao Xiaomei, Midura Sharon, Midura Ronald J, Gorski Jeff P
Biomaterials Section, Department of Oral Biology, School of Dentistry, University of Missouri, Kansas City, Missouri 64108, USA.
J Biol Chem. 2009 Mar 13;284(11):7100-13. doi: 10.1074/jbc.M805898200. Epub 2008 Dec 30.
Mineralization in UMR 106-01 osteoblastic cultures occurs within extracellular biomineralization foci (BMF) within 12 h after addition of beta-glycerol phosphate to cells at 64 h after plating. BMF are identified by their enrichment with an 85-kDa glycoprotein reactive with Maackia amurensis lectin. Laser Raman microspectroscopic scans were made on individual BMF at times preceding (64-76 h) and following the appearance of mineral crystals (76-88 h). The range of variation between spectra for different BMF in the same culture was rather small. In contrast, significant differences were observed for spectral bands at 957-960, 1004, and 1660 cm(-1) when normalized BMF spectra at different times were compared. Protein-dependent spectral bands at 1004 and 1660 cm(-1) increased and then decreased preceding the detection of hydroxyapatite crystals via the phosphate stretching peak at 959-960 cm(-1). When sodium phosphate was substituted for beta-glycerol phosphate, mineralization occurred 3-6 h earlier. Irrespective of phosphate source, the Raman full peak width at half-maximum ratio for 88 h cultures was similar to that for 10-day-old marrow ablation primary bone. However, if mineralization was blocked with serine protease inhibitor 4-(2-aminoethyl)benzenesulfonyl fluoride hydrochloride, 64-88-h BMF spectra remained largely invariant. In summary, Raman spectral data demonstrate for the first time that formation of hydroxyapatite crystals within individual BMF is a multistep process. Second, changes in protein-derived signals at 1004 and 1660 cm(-1) reflect events within BMFs that precede or accompany mineral crystal production because they are blocked by mineralization inhibitor 4-(2-aminoethyl)benzenesulfonyl fluoride hydrochloride. Finally, the low extent of spectral variability detected among different BMF at the same time point indicates that mineralization of individual BMF within a culture is synchronized.
在UMR 106 - 01成骨细胞培养物中,接种64小时后向细胞添加β -甘油磷酸酯,12小时内细胞外生物矿化灶(BMF)内会发生矿化。BMF通过富含一种与黑穗醋栗凝集素反应的85 kDa糖蛋白来识别。在矿物晶体出现之前(64 - 76小时)和之后(76 - 88小时),对单个BMF进行激光拉曼显微光谱扫描。同一培养物中不同BMF的光谱变化范围相当小。相比之下,当比较不同时间的归一化BMF光谱时,在957 - 960、1004和1660 cm⁻¹处的光谱带存在显著差异。在通过959 - 960 cm⁻¹处的磷酸盐伸缩峰检测到羟基磷灰石晶体之前,1004和1660 cm⁻¹处依赖蛋白质的光谱带先增加然后减少。当用磷酸钠替代β -甘油磷酸酯时,矿化提前3 - 6小时发生。无论磷酸盐来源如何,88小时培养物的拉曼半高宽全峰比与10日龄骨髓消融原发性骨的相似。然而,如果用丝氨酸蛋白酶抑制剂4 -(2 -氨基乙基)苯磺酰氟盐酸盐阻断矿化,64 - 88小时的BMF光谱基本保持不变。总之,拉曼光谱数据首次证明单个BMF内羟基磷灰石晶体的形成是一个多步骤过程。其次,1004和1660 cm⁻¹处蛋白质衍生信号的变化反映了BMF内先于或伴随矿物晶体产生的事件,因为它们被矿化抑制剂4 -(2 -氨基乙基)苯磺酰氟盐酸盐阻断。最后,在同一时间点不同BMF之间检测到的光谱变异性程度较低,表明培养物中单个BMF的矿化是同步的。