Three-dimensional viewing of internal cell structure.

Scanning microscopy. Supplement Pub Date : 1989-01-01
G H Haggis
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Abstract

3T3 and HeLa cells, grown as a monolayer, have been rapidly frozen by propane jet as a fresh preparation, without pretreatment. In some experiments the frozen cells were fractured at -170 degrees C, thawed into fixative and viewed by high-resolution SEM after critical-point drying. In other experiments the frozen cells were thawed into fixative unfractured. These preparations were refrozen in 15% methanol, fractured and deep-etched for replication and TEM study. The technique used in this work appears to give rapid rewarming from -170 degrees C to 0 degree C with little evidence of ice crystal growth. The cells fractured before thawing, examined by SEM, show extensive extraction of both nucleus and cytoplasm with deep views of nuclear chromatin, and of cytoplasmic organelles caught amongst rather distorted filaments of the cytoskeleton. Initial fixation for the SEM work was light (0.3% glutaraldehyde for 10 mins) so that structure is seen as it would be retained for antibody labelling.

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细胞内部结构的三维观察。
3T3和HeLa细胞作为单层生长,经丙烷喷射快速冷冻作为新鲜制剂,无需预处理。在一些实验中,冷冻细胞在-170℃下断裂,解冻成固定液,在临界点干燥后用高分辨率扫描电镜观察。在其他实验中,冷冻的细胞被解冻成固定的未断裂的细胞。这些制剂在15%甲醇中重新冷冻,断裂和深蚀刻用于复制和透射电镜研究。这项工作中使用的技术似乎可以从-170摄氏度迅速恢复到0摄氏度,几乎没有冰晶生长的证据。解冻前破裂的细胞,通过扫描电镜检查,显示细胞核和细胞质的广泛提取,细胞核染色质和细胞质细胞器被捕获在相当扭曲的细胞骨架细丝之间。扫描电镜工作的初始固定很轻(0.3%戊二醛固定10分钟),因此可以看到结构,因为它将被保留用于抗体标记。
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