Paul Scherrer Institut, Laboratory for Biomolecular Research, Department of Biology and Chemistry, 5232, Villigen PSI, Switzerland.
Paul Scherrer Institut, Laboratory for Macromolecules and Bioimaging, Department of Synchrotron Radiation and Nanotechnology, 5232, Villigen PSI, Switzerland.
Sci Rep. 2017 Jul 24;7(1):6291. doi: 10.1038/s41598-017-05587-4.
High-throughput three-dimensional cryogenic imaging of thick biological specimens is valuable for identifying biologically- or pathologically-relevant features of interest, especially for subsequent correlative studies. Unfortunately, high-resolution imaging techniques at cryogenic conditions often require sample reduction through sequential physical milling or sectioning for sufficient penetration to generate each image of the 3-D stack. This study represents the first demonstration of using ptychographic hard X-ray tomography at cryogenic temperatures for imaging thick biological tissue in a chemically-fixed, frozen-hydrated state without heavy metal staining and organic solvents. Applied to mammalian brain, this label-free cryogenic imaging method allows visualization of myelinated axons and sub-cellular features such as age-related pigmented cellular inclusions at a spatial resolution of ~100 nanometers and thicknesses approaching 100 microns. Because our approach does not require dehydration, staining or reduction of the sample, we introduce the possibility for subsequent analysis of the same tissue using orthogonal approaches that are expected to yield direct complementary insight to the biological features of interest.
高通量厚生物样本低温三维成像对于识别具有生物学或病理学意义的特征很有价值,特别是对于后续的相关研究。不幸的是,低温条件下的高分辨率成像技术通常需要通过连续的物理铣削或切片来减小样本,以充分穿透生成 3D 堆叠的每个图像。本研究首次展示了在低温下使用相衬硬 X 射线断层扫描技术对化学固定、冷冻水合状态下的厚生物组织进行成像,无需重金属染色和有机溶剂。应用于哺乳动物大脑,这种无标记低温成像方法可以在接近 100 微米的厚度下以约 100 纳米的空间分辨率可视化髓鞘轴突和亚细胞特征,如与年龄相关的色素性细胞内含物。由于我们的方法不需要对样本进行脱水、染色或减小,我们引入了使用正交方法分析同一组织的可能性,预计这些方法将对感兴趣的生物学特征提供直接的补充见解。