Visualization and correction of automated segmentation, tracking and lineaging from 5-D stem cell image sequences

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Abstract

Background: Neural stem cells are motile and proliferative cells that undergo mitosis, dividing to produce daughter cells and ultimately generating differentiated neurons and glia. Understanding the mechanisms controlling neural stem cell proliferation and differentiation will play a key role in the emerging fields of regenerative medicine and cancer therapeutics. Stem cell studies in vitro from 2-D image data are well established. Visualizing and analyzing large three dimensional images of intact tissue is a challenging task. It becomes more difficult as the dimensionality of the image data increases to include time and additional fluorescence channels. There is a pressing need for 5-D image analysis and visualization tools to study cellular dynamics in the intact niche and to quantify the role that environmental factors play in determining cell fate.Results: We present an application that integrates visualization and quantitative analysis of 5-D (x,y,z,t,channel) and large montage confocal fluorescence microscopy images. The image sequences show stem cells together with blood vessels, enabling quantification of the dynamic behaviors of stem cells in relation to their vascular niche, with applications in developmental and cancer biology. Our application automatically segments, tracks, and lineages the image sequence data and then allows the user to view and edit the results of automated algorithms in a stereoscopic 3-D window while simultaneously viewing the stem cell lineage tree in a 2-D window. Using the GPU to store and render the image sequence data enables a hybrid computational approach. An inference-based approach utilizing user-provided edits to automatically correct related mistakes executes interactively on the system CPU while the GPU handles 3-D visualization tasks.Conclusions: By exploiting commodity computer gaming hardware, we have developed an application that can be run in the laboratory to facilitate rapid iteration through biological experiments. We combine unsupervised image analysis algorithms with an interactive visualization of the results. Our validation interface allows for each data set to be corrected to 100% accuracy, ensuring that downstream data analysis is accurate and verifiable. Our tool is the first to combine all of these aspects, leveraging the synergies obtained by utilizing validation information from stereo visualization to improve the low level image processing tasks.

Figures

  • Figure 1 Schematic Diagram of LEVER 3-D. This flow chart shows the process in which LEVER 3-D uses automated algorithms along
  • Figure 2 Reconstruction of an Entire SVZ. The image is the result of registering 34 subsections of a mouse subventricular zone. Registration using only microscope stage position data is indicated with a green dashed line. The blue solid lines represent a max spanning tree indicating which edge of the subsection was registered, e.g. subsection 22 was registered to 18, 21, and 23, where subsection 11 was only registered to 12. The red dashed lines indicate the final position of each subsection after registration. Registration happens in the z direction as well, not shown here.
  • Figure 3 Fully Registered 3-D Montage with 5 Channels. This image has been reconstructed and rendered using the 3-D view window with adjustments made in the transfer function interface in Figure 5. The channels are: blood vessels (red), cell nuclei (dark blue), neural stem cells and astrocytes (green), oligodendrocytes (yellow), and migrating neuroblasts (cyan).
  • Figure 4Mitosis event with lineage tree. The lineage tree in the right panel shows an entire clone starting with the progenitor cell 73 which divides into two daughter cells, 371 and 578. The y-axis represents time where the x-axis represents the cell’s distance to its closest blood vessel. The left panel shows cell 73 in the frame prior to it undergoing mitosis. The center panel shows the frame in which cell 73 divides into cells 371 and 578. The cleavage plane is represented by a white mesh and shows the angle of cleavage relative to the vessel channel. Specimens that are imaged over time typically have fewer channels than static samples. Immunofluorescence can be detrimental to natural cell behavior and has to be used
  • Figure 5 3-D Image viewer and transfer function windows. The right panel shows the controls to set a transfer function which maps the intensity values of the original images into values and colors in the view window. The left panel shows the original image data without any changes to the transfer function. The middle panel shows an image where the transfer function settings shown in the far right panel have been applied.

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Wait, E., Winter, M., Bjornsson, C., Kokovay, E., Wang, Y., Goderie, S., … Cohen, A. R. (2014). Visualization and correction of automated segmentation, tracking and lineaging from 5-D stem cell image sequences. BMC Bioinformatics, 15(1). https://doi.org/10.1186/1471-2105-15-328

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