Three-Dimensional Imaging of Biological Tissue by Cryo X-Ray Ptychography

被引:42
|
作者
Shahmoradian, S. H. [1 ]
Tsai, E. H. R. [2 ]
Diaz, A. [2 ]
Guizar-Sicairos, M. [2 ]
Raabe, J. [3 ]
Spycher, L. [4 ]
Britschgi, M. [4 ]
Ruf, A. [5 ]
Stahlberg, H. [6 ]
Holler, M. [2 ]
机构
[1] Paul Scherrer Inst, Dept Biol & Chem, Lab Biomol Res, CH-5232 Villigen, Switzerland
[2] Paul Scherrer Inst, Dept Synchrotron Radiat & Nanotechnol, Lab Macromol & Bioimaging, CH-5232 Villigen, Switzerland
[3] Paul Scherrer Inst, Dept Synchrotron Radiat & Nanotechnol, Lab Synchrotron Radiat Condensed Matter, CH-5232 Villigen, Switzerland
[4] Roche Innovat Ctr Basel, Roche Pharma Res & Early Dev, NORD DTA, CH-4070 Basel, Switzerland
[5] Roche Innovat Ctr Basel, Roche Pharma Res & Early Dev, Chem Biol, CH-4070 Basel, Switzerland
[6] Univ Basel, Ctr Cellular Imaging & NanoAnalyt C CINA, Biozentrum, CH-4056 Basel, Switzerland
来源
SCIENTIFIC REPORTS | 2017年 / 7卷
基金
瑞士国家科学基金会;
关键词
CELLULAR ULTRASTRUCTURE; CRYOELECTRON TOMOGRAPHY; COMPUTED-TOMOGRAPHY; LIPOFUSCIN; ACCUMULATION; MICROSCOPY; SECTIONS; BRAIN; NEUROMELANIN; MECHANISMS;
D O I
10.1038/s41598-017-05587-4
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
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 similar to 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.
引用
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页数:12
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