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Hierarchical imaging: a new concept for targeted imaging of large volumes from cells to tissues

Wacker, Irene ; Spomer, Waldemar ; Hofmann, Andreas ; Thaler, Marlene ; Hillmer, Stefan ; Gengenbach, Ulrich ; Schröder, Rasmus R.

In: BMC Cell Biology, 17 (2016), Nr. 38. pp. 1-12. ISSN 1471-2121

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Download (6MB) | Lizenz: Creative Commons LizenzvertragHierarchical imaging: a new concept for targeted imaging of large volumes from cells to tissues by Wacker, Irene ; Spomer, Waldemar ; Hofmann, Andreas ; Thaler, Marlene ; Hillmer, Stefan ; Gengenbach, Ulrich ; Schröder, Rasmus R. underlies the terms of Creative Commons Attribution 3.0 Germany

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Abstract

Background: Imaging large volumes such as entire cells or small model organisms at nanoscale resolution seemed an unrealistic, rather tedious task so far. Now, technical advances have lead to several electron microscopy (EM) large volume imaging techniques. One is array tomography, where ribbons of ultrathin serial sections are deposited on solid substrates like silicon wafers or glass coverslips. Results: To ensure reliable retrieval of multiple ribbons from the boat of a diamond knife we introduce a substrate holder with 7 axes of translation or rotation specifically designed for that purpose. With this device we are able to deposit hundreds of sections in an ordered way in an area of 22 × 22 mm, the size of a coverslip. Imaging such arrays in a standard wide field fluorescence microscope produces reconstructions with 200 nm lateral resolution and 100 nm (the section thickness) resolution in z. By hierarchical imaging cascades in the scanning electron microscope (SEM), using a new software platform, we can address volumes from single cells to complete organs. In our first example, a cell population isolated from zebrafish spleen, we characterize different cell types according to their organelle inventory by segmenting 3D reconstructions of complete cells imaged with nanoscale resolution. In addition, by screening large numbers of cells at decreased resolution we can define the percentage at which different cell types are present in our preparation. With the second example, the root tip of cress, we illustrate how combining information from intermediate resolution data with high resolution data from selected regions of interest can drastically reduce the amount of data that has to be recorded. By imaging only the interesting parts of a sample considerably less data need to be stored, handled and eventually analysed. Conclusions: Our custom-designed substrate holder allows reproducible generation of section libraries, which can then be imaged in a hierarchical way. We demonstrate, that EM volume data at different levels of resolution can yield comprehensive information, including statistics, morphology and organization of cells and tissue. We predict, that hierarchical imaging will be a first step in tackling the big data issue inevitably connected with volume EM.

Item Type: Article
Journal or Publication Title: BMC Cell Biology
Volume: 17
Number: 38
Publisher: BioMed Central; Springer
Place of Publication: London; Berlin; Heidelberg
Date Deposited: 15 Dec 2016 13:39
Date: 2016
ISSN: 1471-2121
Page Range: pp. 1-12
Faculties / Institutes: Service facilities > Bioquant
Service facilities > Cluster of Excellence Cellular Networks
Service facilities > Centre for Organismal Studies Heidelberg (COS)
Service facilities > Center for Advanced Materials (CAM)
Subjects: 570 Life sciences
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