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对UMR 106成骨细胞培养物中生物矿化灶进行共聚焦激光拉曼显微光谱分析,结果显示在矿物晶体沉积之前及伴随过程中,蛋白质变化在时间上是同步的。

Confocal laser Raman microspectroscopy of biomineralization foci in UMR 106 osteoblastic cultures reveals temporally synchronized protein changes preceding and accompanying mineral crystal deposition.

作者信息

Wang Chuanyi, Wang Yong, Huffman Nichole T, Cui Chaoying, Yao Xiaomei, Midura Sharon, Midura Ronald J, Gorski Jeff P

机构信息

Biomaterials Section, Department of Oral Biology, School of Dentistry, University of Missouri, Kansas City, Missouri 64108, USA.

出版信息

J Biol Chem. 2009 Mar 13;284(11):7100-13. doi: 10.1074/jbc.M805898200. Epub 2008 Dec 30.

Abstract

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.

摘要

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。

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