Besztejan Stephanie, Keskin Sercan, Manz Stephanie, Kassier Günther, Bücker Robert, Venegas-Rojas Deybith, Trieu Hoc K, Rentmeister Andrea, Miller R J Dwayne
1Chemistry Department,Institute for Biochemistry and Molecular Biology,University of Hamburg,Martin-Luther-King Platz 6,20146 Hamburg,Germany.
3Max Planck Institute for the Structure and Dynamics of Matter,Luruper Chaussee 149,Geb. 99 (CFEL),22761 Hamburg,Germany.
Microsc Microanal. 2017 Feb;23(1):46-55. doi: 10.1017/S1431927616012708. Epub 2017 Jan 31.
We present liquid-cell transmission electron microscopy (liquid-cell TEM) imaging of fixed and non-fixed prostate cancer cells (PC3 and LNCaP) with high resolution in a custom developed silicon nitride liquid cell. Fixed PC3 cells were imaged for 90-120 min without any discernable damage. High contrast on the cellular structures was obtained even at low electron doses (~2.5 e-/nm2 per image). The images show distinct structures of cell compartments (nuclei and nucleoli) and cell boundaries without any further sample embedding, dehydration, or staining. Furthermore, we observed dynamics of vesicles trafficking from the cell membrane in consecutive still frames in a non-fixed cell. Our findings show that liquid-cell TEM, operated at low electron dose, is an excellent tool to investigate dynamic events in non-fixed cells with enough spatial resolution (few nm) and natural amplitude contrast to follow key intracellular processes.
我们展示了在定制开发的氮化硅液体池中对固定和未固定的前列腺癌细胞(PC3和LNCaP)进行的高分辨率液体细胞透射电子显微镜(liquid-cell TEM)成像。固定的PC3细胞成像90 - 120分钟,未出现任何可察觉的损伤。即使在低电子剂量(每张图像约2.5 e - /nm²)下,细胞结构也获得了高对比度。这些图像显示了细胞区室(细胞核和核仁)和细胞边界的清晰结构,无需进一步的样品包埋、脱水或染色。此外,我们在未固定细胞的连续静止帧中观察到了囊泡从细胞膜运输的动态过程。我们的研究结果表明,在低电子剂量下操作的液体细胞TEM是一种出色的工具,能够以足够的空间分辨率(几纳米)和自然的幅度对比度来研究未固定细胞中的动态事件,从而追踪关键的细胞内过程。