Hagen Christoph, Werner Stephan, Carregal-Romero Susana, N Malhas Ashraf, G Klupp Barbara, Guttmann Peter, Rehbein Stefan, Henzler Katja, C Mettenleiter Thomas, J Vaux David, J Parak Wolfgang, Schneider Gerd, Grünewald Kay
Oxford Particle Imaging Centre, Division of Structural Biology, Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford OX3 7BN, UK.
Helmholtz Zentrum Berlin für Materialien und Energie GmbH, Wilhelm-Conrad-Röntgen Campus, 12489 Berlin, Germany.
Ultramicroscopy. 2014 Nov;146:46-54. doi: 10.1016/j.ultramic.2014.05.009. Epub 2014 Jun 3.
Correlative fluorescence and soft X-ray cryo-microscopy/tomography on flat sample holders is perfectly suited to study the uncompromised physiological status of adherent cells at its best possible preservation by imaging after fast cryo-immobilization. To understand the mechanism by which herpesviruses induce nucleoplasmic reticulum, i.e. invaginations of the nuclear envelope, during their egress from the host cell nucleus, morphologically similar structures found in laminopathies and after chemical induction were investigated as a potentially more easily accessible model system. For example, anti-retroviral protease inhibitors like Saquinavir also induce invaginations of the nuclear membranes. With the help of newly designed multimodal nanoparticles as alignment and correlation markers, and by optimizing fluorescence cryo-microscopy data acquisition, an elaborate three-dimensional network of nucleoplasmic reticulum was demonstrated in nuclei of Saquinavir-treated rabbit kidney cells expressing a fluorescently labeled inner nuclear membrane protein. In part of the protease inhibitor-treated samples, nuclei exhibited dramatic ultrastructural changes indicative of programmed cell death/apoptosis. This unexpected observation highlights another unique feature of soft X-ray microscopy, i.e. high absorption contrast information not relying on labeled cellular components, at a 3D resolution of approximately 40 nm (half-pitch) and through a sample thickness of several micrometers. These properties make it a valuable part of the cell biology imaging toolbox to visualize the cellular ultrastructure in its completeness.
在扁平样品架上进行相关荧光和软X射线冷冻显微镜/断层扫描,非常适合通过快速冷冻固定后的成像来研究贴壁细胞在尽可能最佳保存状态下的未受损害的生理状态。为了理解疱疹病毒在从宿主细胞核逸出过程中诱导核质网(即核膜内陷)的机制,对在核纤层病中以及化学诱导后发现的形态学上相似的结构进行了研究,作为一个可能更容易获取的模型系统。例如,抗逆转录病毒蛋白酶抑制剂如沙奎那韦也会诱导核膜内陷。借助新设计的多模态纳米颗粒作为对齐和相关标记,并通过优化荧光冷冻显微镜数据采集,在表达荧光标记的内核膜蛋白的沙奎那韦处理的兔肾细胞核中展示了一个精细的核质网三维网络。在部分蛋白酶抑制剂处理的样品中,细胞核表现出指示程序性细胞死亡/凋亡的显著超微结构变化。这一意外发现凸显了软X射线显微镜的另一个独特特征,即在约40纳米(半间距)的三维分辨率和穿过几微米的样品厚度下,不依赖标记细胞成分的高吸收对比信息。这些特性使其成为细胞生物学成像工具箱中一个有价值的部分,能够完整地可视化细胞超微结构。