首页> 外文期刊>Proceedings of the National Academy of Sciences of the United States of America >HIGH RESOLUTION ULTRASTRUCTURAL MAPPING OF TOTAL CALCIUM - ELECTRON SPECTROSCOPIC IMAGING ELECTRON ENERGY LOSS SPECTROSCOPY ANALYSIS OF A PHYSICALLY/CHEMICALLY PROCESSED NERVE-MUSCLE PREPARATION
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HIGH RESOLUTION ULTRASTRUCTURAL MAPPING OF TOTAL CALCIUM - ELECTRON SPECTROSCOPIC IMAGING ELECTRON ENERGY LOSS SPECTROSCOPY ANALYSIS OF A PHYSICALLY/CHEMICALLY PROCESSED NERVE-MUSCLE PREPARATION

机译:物理/化学过程神经肌肉制备的总钙-电子光谱成像电子能量损失谱的高分辨率超微结构映射

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We report on a procedure for tissue preparation that combines thoroughly controlled physical and chemical treatments: quick-freezing and freeze-drying followed by fixation with OsO4 vapors and embedding by direct resin infiltration. Specimens of frog cutaneous pectoris muscle thus prepared were analyzed for total calcium using electron spectroscopic imaging/electron energy loss spectroscopy (ESI/EELS) approach. The preservation of the ultrastructure was excellent, with positive K/Na ratios revealed in the fibers by x-ray microanalysis. Clear, high-resolution EELS/ESI calcium signals were recorded from the lumen of terminal cisternae of the sarcoplasmic reticulum but not from longitudinal cisternae, as expected from previous studies carried out with different techniques. In many mitochondria, calcium was below detection whereas in others it was appreciable although at variable level. Within the motor nerve terminals, synaptic vesicles as well as some cisternae of the smooth endoplasmic reticulum yielded positive signals at variance with mitochondria, that were most often below detection. Taken as a whole, the present study reveals the potential of our experimental approach to map with high spatial resolution the total calcium within individual intracellular organelles identified by their established ultrastructure, but only where the element is present at high levels. [References: 50]
机译:我们报告了一种结合了彻底控制的物理和化学处理的组织准备程序:快速冷冻和冷冻干燥,然后用OsO4蒸气固定,并通过直接树脂渗透进行包埋。使用电子光谱成像/电子能量损失光谱法(ESI / EELS)方法分析由此制备的青蛙皮肤胸肌标本的总钙。超微结构的保存效果极好,通过X射线微分析显示出纤维中的正K / Na比为正。如先前使用不同技术进行的研究所预期的那样,从肌浆网终末池的腔中记录了清晰的高分辨率EELS / ESI钙信号,而从纵池中未记录到。在许多线粒体中,钙含量低于检测水平,而在其他线粒体中,钙含量虽然有所变化,但仍是可观的。在运动神经末梢内,突触小泡以及平滑内质网的某些池产生与线粒体有差异的阳性信号,这些信号最常被检测不到。总的来说,本研究揭示了我们的实验方法的潜力,即以高空间分辨率绘制由已建立的超微结构识别的单个细胞内细胞器内总钙的图谱,但仅当元素以高水平存在时才如此。 [参考:50]

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