Live Cell Imaging of Mitosis
Mitosis is a form of cell division in which a cell’s genetic material is divided equally between two daughter cells. Mitosis can be broken down into s…
Mitosis is the highly organized and controlled division of nuclear contents that occurs during the cell cycle. Mitosis is fundamentally important for proper organismal development, and for tissue growth, maintenance, and repair. Disruption of this process has been indicated in certain diseases, like cancer. Live cell imaging via time-lapse fluorescent microscopy is one of the most common methods of studying mitosis in labs today.
In this video, we’ll briefly introduce the phases of mitosis, and then discuss experimental considerations for live cell imaging of this cellular process. A detailed data acquisition and analysis protocol will be shown, and we’ll wrap up with a few applications of this technique.
To better understand what scientists are looking for in these imaging experiments, let’s first walk through the stages of mitosis.
The cell cycle describes the overall process of cell growth and division. The mitotic phase represents one short portion of this cycle, which can be further broken down into six phases: namely prophase, prometaphase, metaphase, anaphase, telophase, and cytokinesis.
During prophase, the DNA condenses into sister chromatids joined at the centromere. In the cytoplasm, two key organelles referred to as centrosomes begin assembling microtubule structures—commonly known as spindle fibers—in a wheel-like pattern.
The next phase, prometaphase, sees the breakdown of the nuclear membrane, and assembly of a complex of proteins, known as the kinetochore, at the centromeres. This phase also witnesses the linkage of the spindle fibers with the kinetochore.
In metaphase, the chromosomes line up at the metaphase plate, an imaginary plane equidistant from the two centromeres. During anaphase, chromosomes “break apart” at the centromere, with individual sister chromatids migrating to the opposite ends of the cell. In telophase, the mitotic spindle disassembles and the chromatin begins to decondense. Finally, during cytokinesis—via contraction of an actin/myosin ring that forms the “cleavage furrow”—the parent cell divides into two daughter cells.
With this understanding of mitotic progression, let’s take a look at the practical considerations for viewing this process using live cell imaging.
The first question to ask is: how to label cells in order to visualize mitosis? The most commonly employed “tags” for this experiment are fluorescent molecules, which absorb light at one wavelength and emit light at another wavelength.
In order to label nucleic acids, one can use a cell permeable DNA binding dye, like Hoechst. For labeling proteins such as microtubules, one can use fluorescently tagged antibodies. These are generally membrane impermeable, and therefore microinjection techniques are employed to insert them into samples.
Another strategy is genetic labeling, in which cells can be manipulated to express fluorescently tagged proteins that label components actively involved in mitosis, such as chromosomes. When working with fluorescent molecules, you must avoid excessive exposure to light to avoid photobleaching.
Choosing the right microscope is an equally important decision. The two most commonly used microscopes are epifluorescent and confocal. Epifluorescent or wide field microscopy passes light over the entire field of view, while confocal microscopy uses lasers to focus light onto single points.
While epifluorescent microscopes are typically cheaper, confocal microscopes are preferred as the point illumination provides increased optical resolution, producing clearer images. The single point of illumination also reduces phototoxicity, or increased cell death caused by excessive exposure to light.
Now that we’ve reviewed some experimental considerations, let’s see how to run a live cell imaging experiment for visualizing mitosis.
Cells should be cultured on glass bottom dishes or on coverslips, which allows for the best visualization of mitosis. Next, they should be maintained in a controlled envioronment until labeling is performed. As mentioned earlier, the choice of labeling technique depends on the experiment at hand. After labeling, place the cell culture dish into the specialized chamber on the microscope. This allows cell culture conditions to be maintained during imaging.
Next, depending on the labeling molecule, set the excitation and emission wavelengths on the microscope. For data acquisition, setup time points and position for image capture. In this context, time points are the instances at which images will be acquired to provide complete visual coverage for all mitotic stages. Positions refer to the X-Y coordinates on the culture dish. In addition, for each position one can acquire images at different depths of field. Each image represents an optical slice on the Z-axis. Therefore, they are collectively known as Z-stacks. After entering all parameters, test the settings and then sit back and enjoy!
Having acquired the time-lapse data, there are several ways to present it. Let’s discuss a few of these ways.
A montage is one of the most common ways to present time-lapse data, where multiple images are arrayed in a grid-like pattern based on time. These can clearly show mitotic progression, and allow researchers to determine information such as time spent in individual mitotic phases. Combining these images sequentially to make a “movie” can be a more dynamic presentation.
Lastly, Z-stacks obtained using a confocal microscope can be combined to present a 3D recreation of a sample. This can accurately reveal spatial relationships between pieces of the mitotic machinery. This is important since components that look next to each other in 2D may actually be far apart in three dimensions.
Now that you know how to run a live cell imaging experiment, let’s review some applications of this technique.
Mitosis is an essential part of development. Here, researchers isolated embryonic mouse brains to observe mitosis in neural progenitor cells. Controlled division of these cells is critical for proper brain growth and function. Following isolation, brains were sectioned using a vibratome, stained with membrane permeable nucleic acid-binding dye, and imaged via confocal microscopy to clearly visualize mitosis of neural progenitor cells.
DNA repair is a critical cellular process that is involved in cell growth and division. In this experiment, researchers studied a DNA repair protein that forms foci, which are punctate spots created in response to DNA damage. Results of live cell imaging and 3D analysis highlighted the localization of the DNA repair protein throughout the cell division process.
Finally, researchers study mitotic checkpoints, which are “pause” points where cellular conditions are assessed before division continues. In mitosis, the spindle assembly checkpoint, or SAC, ensures proper connection between the mitotic spindle and the chromosomes. To study this, scientists microinjected SAC-inducing reagents into transgenic fly embryos, and analyzed mitosis using live cell imaging. Results show arrested kinetochores, demonstrating cells that fail to progress through mitosis.
You’ve just watched JoVE’s video on live cell imaging of mitosis. Following an introduction to the stages of mitosis, this video introduced important considerations and data analysis techniques for live cell imaging. Finally, applications of this technique were presented. Live cell imaging has substantially helped scientists in understanding mitotic mechanisms related to development, tissue maintenance, and disease. As always, thanks for watching!
Mitosis is the highly organized and controlled division of nuclear contents that occurs during the cell cycle. Mitosis is fundamentally important for proper organismal development, and for tissue growth, maintenance, and repair. Disruption of this process has been indicated in certain diseases, like cancer. Live cell imaging via time-lapse fluorescent microscopy is one of the most common methods of studying mitosis in labs today.
In this video, we’ll briefly introduce the phases of mitosis, and then discuss experimental considerations for live cell imaging of this cellular process. A detailed data acquisition and analysis protocol will be shown, and we’ll wrap up with a few applications of this technique.
To better understand what scientists are looking for in these imaging experiments, let’s first walk through the stages of mitosis.
The cell cycle describes the overall process of cell growth and division. The mitotic phase represents one short portion of this cycle, which can be further broken down into six phases: namely prophase, prometaphase, metaphase, anaphase, telophase, and cytokinesis.
During prophase, the DNA condenses into sister chromatids joined at the centromere. In the cytoplasm, two key organelles referred to as centrosomes begin assembling microtubule structures—commonly known as spindle fibers—in a wheel-like pattern.
The next phase, prometaphase, sees the breakdown of the nuclear membrane, and assembly of a complex of proteins, known as the kinetochore, at the centromeres. This phase also witnesses the linkage of the spindle fibers with the kinetochore.
In metaphase, the chromosomes line up at the metaphase plate, an imaginary plane equidistant from the two centromeres. During anaphase, chromosomes “break apart” at the centromere, with individual sister chromatids migrating to the opposite ends of the cell. In telophase, the mitotic spindle disassembles and the chromatin begins to decondense. Finally, during cytokinesis—via contraction of an actin/myosin ring that forms the “cleavage furrow”—the parent cell divides into two daughter cells.
With this understanding of mitotic progression, let’s take a look at the practical considerations for viewing this process using live cell imaging.
The first question to ask is: how to label cells in order to visualize mitosis? The most commonly employed “tags” for this experiment are fluorescent molecules, which absorb light at one wavelength and emit light at another wavelength.
In order to label nucleic acids, one can use a cell permeable DNA binding dye, like Hoechst. For labeling proteins such as microtubules, one can use fluorescently tagged antibodies. These are generally membrane impermeable, and therefore microinjection techniques are employed to insert them into samples.
Another strategy is genetic labeling, in which cells can be manipulated to express fluorescently tagged proteins that label components actively involved in mitosis, such as chromosomes. When working with fluorescent molecules, you must avoid excessive exposure to light to avoid photobleaching.
Choosing the right microscope is an equally important decision. The two most commonly used microscopes are epifluorescent and confocal. Epifluorescent or wide field microscopy passes light over the entire field of view, while confocal microscopy uses lasers to focus light onto single points.
While epifluorescent microscopes are typically cheaper, confocal microscopes are preferred as the point illumination provides increased optical resolution, producing clearer images. The single point of illumination also reduces phototoxicity, or increased cell death caused by excessive exposure to light.
Now that we’ve reviewed some experimental considerations, let’s see how to run a live cell imaging experiment for visualizing mitosis.
Cells should be cultured on glass bottom dishes or on coverslips, which allows for the best visualization of mitosis. Next, they should be maintained in a controlled envioronment until labeling is performed. As mentioned earlier, the choice of labeling technique depends on the experiment at hand. After labeling, place the cell culture dish into the specialized chamber on the microscope. This allows cell culture conditions to be maintained during imaging.
Next, depending on the labeling molecule, set the excitation and emission wavelengths on the microscope. For data acquisition, setup time points and position for image capture. In this context, time points are the instances at which images will be acquired to provide complete visual coverage for all mitotic stages. Positions refer to the X-Y coordinates on the culture dish. In addition, for each position one can acquire images at different depths of field. Each image represents an optical slice on the Z-axis. Therefore, they are collectively known as Z-stacks. After entering all parameters, test the settings and then sit back and enjoy!
Having acquired the time-lapse data, there are several ways to present it. Let’s discuss a few of these ways.
A montage is one of the most common ways to present time-lapse data, where multiple images are arrayed in a grid-like pattern based on time. These can clearly show mitotic progression, and allow researchers to determine information such as time spent in individual mitotic phases. Combining these images sequentially to make a “movie” can be a more dynamic presentation.
Lastly, Z-stacks obtained using a confocal microscope can be combined to present a 3D recreation of a sample. This can accurately reveal spatial relationships between pieces of the mitotic machinery. This is important since components that look next to each other in 2D may actually be far apart in three dimensions.
Now that you know how to run a live cell imaging experiment, let’s review some applications of this technique.
Mitosis is an essential part of development. Here, researchers isolated embryonic mouse brains to observe mitosis in neural progenitor cells. Controlled division of these cells is critical for proper brain growth and function. Following isolation, brains were sectioned using a vibratome, stained with membrane permeable nucleic acid-binding dye, and imaged via confocal microscopy to clearly visualize mitosis of neural progenitor cells.
DNA repair is a critical cellular process that is involved in cell growth and division. In this experiment, researchers studied a DNA repair protein that forms foci, which are punctate spots created in response to DNA damage. Results of live cell imaging and 3D analysis highlighted the localization of the DNA repair protein throughout the cell division process.
Finally, researchers study mitotic checkpoints, which are “pause” points where cellular conditions are assessed before division continues. In mitosis, the spindle assembly checkpoint, or SAC, ensures proper connection between the mitotic spindle and the chromosomes. To study this, scientists microinjected SAC-inducing reagents into transgenic fly embryos, and analyzed mitosis using live cell imaging. Results show arrested kinetochores, demonstrating cells that fail to progress through mitosis.
You’ve just watched JoVE’s video on live cell imaging of mitosis. Following an introduction to the stages of mitosis, this video introduced important considerations and data analysis techniques for live cell imaging. Finally, applications of this technique were presented. Live cell imaging has substantially helped scientists in understanding mitotic mechanisms related to development, tissue maintenance, and disease. As always, thanks for watching!
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Q1: What are the six phases of mitosis?
Mitosis consists of prophase, prometaphase, metaphase, anaphase, telophase, and cytokinesis. During prophase, DNA condenses into sister chromatids and centrosomes assemble spindle fibers. Prometaphase involves nuclear membrane breakdown and kinetochore assembly. Metaphase aligns chromosomes at the metaphase plate. Anaphase separates sister chromatids to opposite cell ends. Telophase disassembles the spindle and decondenses chromatin. Cytokinesis divides the parent cell into two daughter cells via an actin/myosin cleavage furrow.
Q2: How do scientists label cells for live cell imaging of mitosis?
Scientists use fluorescent molecules that absorb light at one wavelength and emit at another. DNA binding dyes like Hoechst label nucleic acids and are cell permeable. Fluorescently tagged antibodies label proteins such as microtubules but require microinjection since they're membrane impermeable. Genetic labeling allows cells to express fluorescently tagged proteins that mark mitotic components like chromosomes. Excessive light exposure must be avoided to prevent photobleaching.
Q3: Why is confocal microscopy preferred over epifluorescent microscopy for mitosis imaging?
Confocal microscopy uses lasers to focus light onto single points, providing increased optical resolution and clearer images compared to epifluorescent microscopy, which passes light over the entire field of view. The point illumination in confocal microscopy also reduces phototoxicity, or increased cell death caused by excessive light exposure. Although confocal microscopes are more expensive, their superior image quality and reduced cell damage make them the preferred choice for detailed mitotic visualization.
Q4: What are Z-stacks and why are they important in mitosis imaging?
Z-stacks are multiple optical slices captured at different depths of field along the Z-axis for each position on the culture dish. They allow researchers to reconstruct three-dimensional images of mitotic cells, accurately revealing spatial relationships between mitotic machinery components. This is critical because structures appearing adjacent in two-dimensional images may actually be far apart in three dimensions, providing essential information about the true organization of the dividing cell.
Q5: How are time-lapse imaging results typically presented to show mitotic progression?
Montages are the most common presentation method, displaying multiple images in a grid-like pattern based on time to clearly show mitotic progression and allow determination of time spent in individual phases. Sequential combination of these images creates dynamic movies for more engaging presentation. Confocal Z-stacks can be combined to generate 3D recreations that reveal spatial relationships between mitotic components with greater accuracy than 2D analysis alone.
Q6: What experimental setup is required before acquiring live cell imaging data?
Cells must be cultured on glass bottom dishes or coverslips for optimal visualization. They're maintained in a controlled environment until labeling is performed using the appropriate technique. After labeling, the culture dish is placed into a specialized microscope chamber that maintains cell culture conditions during imaging. Excitation and emission wavelengths are set based on the labeling molecule, and time points and X-Y positions are configured to capture complete coverage of all mitotic stages.
Q7: How is live cell imaging of mitosis applied to studying cell division?
Live cell imaging reveals mitotic mechanisms critical for understanding cell division proliferation cancer and development. Researchers use it to observe neural progenitor cell division during brain development, track DNA repair protein localization throughout division, and study spindle assembly checkpoints that pause division when chromosomes aren't properly connected. These applications have substantially helped scientists understand how mitosis is biologically controlled and how disruption of this process contributes to diseases like cancer.