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用于观察快速冷冻生物标本细胞内结构的高分辨率低温扫描电子显微镜。

High-resolution low-temperature scanning electron microscopy for observing intracellular structures of quick frozen biological specimens.

作者信息

Inoué T, Koike H

机构信息

Department of Anatomy, Tottori University School of Medicine, Yonago, Japan.

出版信息

J Microsc. 1989 Nov;156(Pt 2):137-47. doi: 10.1111/j.1365-2818.1989.tb02913.x.

Abstract

Intracellular structures of rapidly frozen biological tissues were observed in 3-D under a low-temperature scanning electron microscope using a newly developed side-entry type cryo-holder. The present low-temperature SEM is simple, easy to operate and effective for observing biological materials at high magnification. Biological tissues (the pancreas, small intestine, brown adipose tissue and Harderian gland) freshly removed from the mouse were immediately frozen in liquid propane cooled with liquid nitrogen, and their surfaces were manually fractured using a precooled razor blade in liquid nitrogen before introducing the cryo-holder into the SEM. When intracellular structures were revealed after appropriate sublimation, the specimens were coated with gold using a metal evaporator fitted to the side of the microscope column at one of the specimen chamber ports. The cryo-holder was connected to a copper braid coming from a liquid nitrogen reservoir to maintain a low temperature. Using this method, intracellular structures such as the mitochondria and endoplasmic reticulum were demonstrated at high magnifications. Ribosomal granules were discerned on the rough endoplasmic reticulum of the pancreatic acinar cells. Granular substances, presumably elementary particles, were also recognized on the mitochondrial cristae of the brown adipose tissue. The method was particularly effective for studying the 3-D configuration of lipid droplets which had been difficult to preserve by chemical fixation.

摘要

使用新开发的侧入式低温样品台,在低温扫描电子显微镜下对快速冷冻的生物组织的细胞内结构进行了三维观察。目前的低温扫描电子显微镜结构简单、易于操作,并且在高倍放大观察生物材料方面很有效。从小鼠身上新鲜取出的生物组织(胰腺、小肠、棕色脂肪组织和哈德氏腺)立即在液氮冷却的液态丙烷中冷冻,在将低温样品台引入扫描电子显微镜之前,在液氮中用预冷的剃须刀片手动将其表面切开。当经过适当升华后细胞内结构显现出来时,在样品室端口之一处使用安装在显微镜柱侧面的金属蒸发器对样品进行金涂层处理。低温样品台连接到来自液氮储存器的铜编织物上以保持低温。使用这种方法,在高倍放大下展示了线粒体和内质网等细胞内结构。在胰腺腺泡细胞的糙面内质网上可以辨别出核糖体颗粒。在棕色脂肪组织的线粒体嵴上也识别出了颗粒物质,推测为基本粒子。该方法对于研究难以通过化学固定保存的脂滴的三维结构特别有效。

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