Togo Akinobu, Ohta Keisuke, Higashi Ryuhei, Nakamura Kei-Ichiro
Electron Microscopic Unit, Kurume University school of Medicine 67 Asahi machi, Kurume, Fukuoka, Japan.
Division of Microscopic and Development Anatomy, Department of Anatomy, Kurume university school of Medicine 67 Asahi machi, Kurume, Fukuoka, Japan.
Microscopy (Oxf). 2014 Nov;63 Suppl 1:i34-i35. doi: 10.1093/jmicro/dfu078.
IntroductionBecause recent three-dimensional (3D) ultrastructural reconstruction techniques such as serial block face scanning electron microscopy (SBFSEM), obtain their images directly from the flat surface of specimens via material contrast[1], specimens should be strongly stained with heavy metals prior to resin embedding in order to obtain higher material contrast using backscattered electrons (BSEs). To enhance membrane contrast for block face imaging (BFI), we usually stain specimens using the method published by Deerinck[2], and the images obtained show TEM-like contrast.However, recently, our research subjects have required reconstruction of a much larger volume, increasing the total image acquisition time. To reduce the total acquisition time, both high sensitivity detectors and a new specimen preparation method that provides much higher contrast are required. Takahashi et al.[3] have reported that hydroquinone (HQ) treatment during traditional electro-conductive staining increases specimen conductivity and drastically reduces the charge problem for SEM observation. They concluded that HQ treatment might increase the efficiency of secondary electron (SE) generation. Because BFI can be performed using SE as well as BSE, we examined whether addition of HQ treatment to en bloc staining protocols increased the contrast for BFI using SE. Materials & methodsMouse liver tissue was used. Mice were deeply anesthetized by diethyl ether and sodium pentobarbital, and tissues were fixed by transcardial perfusion of 2% paraformaldehyde and 2.5% glutaraldehyde in 0.1 M cacodylate buffer (pH 7.4) through the left ventricle, followed by heparin-containing saline. After perfusion, liver tissues were removed and cut into small cubes approximately 1 mm(3) in the fixative, and were further fixed in the same fixative for 2 h at 4°C. Subsequently, en blocstaining was performed as follows: the specimens were treated using a reduced-OTO staining method (1.5% potassium ferrocyanide-2% OsO4, 1% thiocarbohydrazide, and then 2% OsO4). Subsequently, specimens were treated with 1% HQ solution. Some specimens were exempted from this step and used as controls. Specimens were further stained with 4% uranyl acetate and Walton's lead aspartate solution.After staining, specimens were dehydrated using an ethanol series and embedded in epoxy resin (EPON812, TAAB). Surface of specimens block were cut with a diamond knife, and the newly created flat surfaces of the specimens were coated with evaporated carbon (50 Å) and observed using a SEM (Quanta 3D FEG, FEI).ResultsThe HQ-treated specimens generated a larger amount of SEs than control specimens when subjected to irradiation with the same beam, although BSE numbers were not evidently increased by the treatment. The present results suggest that HQ treatment increases SE generation efficiency, but does not enhance the recruitment of heavy metals into specimens. HQ treatment increased the contrast-to-noise ratio of BFI for images obtained using SEs, and may reduce the total image acquisition time of recently developed 3D reconstruction methods based on SEM.
引言
由于诸如连续块面扫描电子显微镜(SBFSEM)等近期的三维(3D)超微结构重建技术是通过材料对比度直接从标本的平坦表面获取图像[1],因此在树脂包埋之前,标本应使用重金属进行强烈染色,以便利用背散射电子(BSE)获得更高的材料对比度。为了增强块面成像(BFI)的膜对比度,我们通常使用Deerinck发表的方法对标本进行染色[2],所获得的图像显示出类似透射电子显微镜(TEM)的对比度。
然而,最近,我们的研究对象需要重建更大的体积,这增加了总图像采集时间。为了减少总采集时间,既需要高灵敏度探测器,也需要一种能提供更高对比度的新标本制备方法。高桥等人[3]报道,在传统的导电染色过程中进行对苯二酚(HQ)处理可提高标本的导电性,并大幅减少扫描电子显微镜(SEM)观察中的电荷问题。他们得出结论,HQ处理可能会提高二次电子(SE)的产生效率。由于BFI既可以使用SE也可以使用BSE来进行,我们研究了在整体染色方案中添加HQ处理是否会增加使用SE进行BFI的对比度。
材料与方法
使用小鼠肝脏组织。小鼠通过乙醚和戊巴比妥钠深度麻醉,然后通过左心室经心内灌注0.1 M二甲胂酸钠缓冲液(pH 7.4)中的2%多聚甲醛和2.5%戊二醛进行组织固定,随后灌注含肝素的生理盐水。灌注后,取出肝脏组织并在固定剂中切成约1立方毫米的小方块,并在4°C下在相同固定剂中进一步固定2小时。
随后,按以下方式进行整体染色:标本采用改良的OTO染色法(1.5%亚铁氰化钾 - 2%四氧化锇、1%硫代碳酰肼,然后是2%四氧化锇)处理。随后,标本用1% HQ溶液处理。一些标本不进行此步骤用作对照。标本再用4%醋酸铀和沃尔顿天冬氨酸铅溶液染色。
染色后,标本用乙醇系列脱水并包埋在环氧树脂(EPON812,TAAB)中。用金刚石刀切割标本块的表面,标本新形成的平坦表面用蒸发碳(50 Å)涂层,并使用SEM(Quanta 3D FEG,FEI)观察。
结果
当用相同束流照射时,经HQ处理的标本比对照标本产生更多的SE,尽管该处理并未明显增加BSE的数量。目前的结果表明,HQ处理提高了SE的产生效率,但并未增强重金属进入标本的量。HQ处理提高了使用SE获得的BFI图像的对比度噪声比,并可能减少基于SEM的近期开发的3D重建方法的总图像采集时间。