Ryall Rosemary Lyons, Grover Phulwinder K, Thurgood Lauren A, Chauvet Magali C, Fleming David E, van Bronswijk Wilhelm
Department of Surgery, Flinders Medical Centre, Flinders University School of Medicine, Bedford Park, SA, 5042, Australia.
Urol Res. 2007 Feb;35(1):1-14. doi: 10.1007/s00240-007-0078-4. Epub 2007 Feb 3.
This study was undertaken to determine whether the use of different washing procedures could explain dissident findings in published studies examining the role of urinary macromolecules in urolithiasis. Calcium oxalate monohydrate (COM) crystals were deposited from or added to the same sieved urine, washed with copious or limited amounts of distilled water, or with methanol, and examined by field emission scanning electron microscopy (FESEM). Demineralized extracts were analysed by SDS-PAGE and Western blotting for Tamm-Horsfall glycoprotein (THG), human serum albumin (HSA), osteopontin (OPN) and prothrombin fragment 1 (PTF1). Synchrotron X-ray diffraction (SXRD) with Rietveld whole-pattern peak fitting and profile analysis was used to determine non-uniform crystal strain and crystallite size in crystals generated from inorganic solutions in the presence of increasing concentrations of THG and prothrombin (PT). HSA and PTF1 were present in all demineralized crystal extracts, confirming their inclusion within COM. OPN was present in all extracts except those derived from pure inorganic COM crystals, because of its occlusion within small numbers of calcium oxalate dihydrate (COD) crystals contaminating the COM population. THG was absent from the demineralized extracts of all crystals washed copiously with water, but present in those washed with methanol or limited amounts of water. FESEM showed extraneous organic material associated only with crystals whose extracts contained THG, confirming that the protein does not bind permanently to the COM crystal surface and is not occluded within the mineral bulk. This was confirmed by SXRD, which showed that non-uniform strain and crystallite size remained unaltered in crystals grown in the presence of increasing THG concentrations. However, non-uniform strain increased and crystallite size decreased with increasing PT concentrations, demonstrating unambiguously that PT is included in COM crystals. It was concluded that scrupulous care must be taken to ensure the complete removal of extraneous THG adventitiously associated with CaOx crystals in order to avoid inaccurate analysis of crystal matrix protein content and possible misinterpretation of experimental data.
本研究旨在确定不同的清洗程序是否能够解释已发表研究中关于尿大分子在尿路结石形成中的作用的不一致结果。将一水合草酸钙(COM)晶体从同一经过筛分的尿液中沉积或添加到其中,分别用大量或少量蒸馏水、甲醇进行洗涤,然后通过场发射扫描电子显微镜(FESEM)进行检测。通过SDS-PAGE和蛋白质印迹法对脱矿质提取物进行分析,以检测Tamm-Horsfall糖蛋白(THG)、人血清白蛋白(HSA)、骨桥蛋白(OPN)和凝血酶原片段1(PTF1)。利用同步辐射X射线衍射(SXRD)结合Rietveld全谱峰拟合和轮廓分析,来确定在THG和凝血酶原(PT)浓度不断增加的情况下,由无机溶液生成的晶体中的非均匀晶体应变和微晶尺寸。所有脱矿质晶体提取物中均存在HSA和PTF1,证实它们包含在COM中。除了来自纯无机COM晶体的提取物外,所有提取物中均存在OPN,这是因为它被少量污染COM群体的二水合草酸钙(COD)晶体所包裹。用水大量洗涤的所有晶体的脱矿质提取物中均不存在THG,但在用甲醇或少量水洗涤的提取物中存在。FESEM显示,仅与提取物中含有THG的晶体相关的外来有机物质,证实该蛋白质不会永久结合到COM晶体表面,也不会被包裹在矿物质块中。SXRD证实了这一点,其表明在THG浓度不断增加的情况下生长的晶体中,非均匀应变和微晶尺寸保持不变。然而,随着PT浓度的增加,非均匀应变增加而微晶尺寸减小,明确表明PT包含在COM晶体中。研究得出结论,必须格外小心,以确保彻底去除与草酸钙晶体偶然相关的外来THG,以避免对晶体基质蛋白含量的不准确分析以及对实验数据的可能误读。