We want to thank Alessandro Vercelli for the critical comments and Sartorius&#39;s technical support for the help. Our research on these topics has been generously supported by the Rita-Levi Montalcini Grant 2021 (MIUR, Italy). This research was funded by Ministero dell&#39;Istruzione dell&#39;Universit&#224; e della Ricerca MIUR project Dipartimenti di Eccellenza 2023-2027 to Department of Neuroscience Rita Levi Montalcini. D.M.R.&#39;s research has been conducted during and with the support of the Italian national inter-university PhD course in Sustainable Development and Climate Change (link: www.phd-sdc.it).

1. Scanning the vessel on the machine
NOTE: The detection is performed by the built-in Basler Ace 1920-155 &#181;m camera.
<ol>
	<li>Open the program by clicking Connect to Device and selecting Schedule - To Acquire. Then click the + sign.</li>
	<li>Specify whether the vessel will be scanned repeatedly or only 1x by choosing the option Scan on Schedule or Scan Once Now, respectively.</li>
	<li>Select New to create a brand-new vessel to scan. If a new vessel is not added, create a new scan using one of the options described below.
	<ol>
		<li>Select Copy Current to create a new vessel by copying a vessel from the current schedule. Select Copy Previous to create a new vessel by copying a previously scanned vessel.</li>
		<li>Select Add Scan to restore a previously scanned vessel for additional scans.</li>
	</ol>
	</li>
	<li>Select the scan type based on the assay and application. For the analysis, select Standard.</li>
	<li>Specify scan settings. Choose one of the Cell-by-Cell options, either None, Adherent Cell-by-Cell, or Non-adherent Cell-by-Cell, and specify the image channels depending on the fluorescent molecules utilized. Select the None option for adult and embryonic sensory neuron cultures. For cell lines, select None or Adherent Cell-by-Cell options.</li>
	<li>Select the microscope objective (4x, 10x, 20x). Acquire with the higher magnification (20x) in primary cultures, while in cell lines, 10x is sufficient.</li>
	<li>Select the type of vessel to scan from the options provided. Indicate the vessel&#39;s location in the drawer by selecting its position on the virtual map of the drawer.</li>
	<li>Specify the scan pattern for the image acquisition by selecting the wells to scan. Select the desired number of images per well. An estimation of the scan duration will appear.</li>
	<li>Provide information about the vessel by typing the name and specify the plate map by clicking on the + sign.</li>
	<li>Click Next. Choose the Analysis Type, and click Next. A summary screen of the selected options will appear. If correct, click on Scan Now and the scan will start.</li>
</ol>
2. Setup for phase contrast image analysis
NOTE: Neurotrack analysis can only be performed on images previously acquired by the machine.
<ol>
	<li>Select the Scanned Vessel to analyze. Select Launch Analysis. Select Create New Analysis Definition.</li>
	<li>Select Neurotrack. Select Image Channels. Select a representative set of images to perform the analysis on. Select all images for each well to train the algorithm.</li>
	<li>Refine the Analysis Definition settings by adjusting the following parameters. 
	NOTE: By default, neurites are segmented in magenta, whereas cell bodies in yellow. It is possible to modify the colors as desired.
	<ol>
		<li>For cell-body cluster segmentation, adjust the following as described below.
		<ol>
			<li>Segmentation mode: The images&#39; segmentation is done to distinguish cell bodies from background and neurites. Choose between Brightness and Texture. For primary cultures and cell lines select Brightness mode.</li>
			<li>Segmentation adjustment: Use the slider to adjust the segmentation sensitivity toward more background or more cells. It ranges from 0 (Background) to 2 (Cells). It increases or decreases the size of the yellow mask. Move the slider towards 0 (Background) so the size of the yellow mask will gradually reduce leaving space for the magenta mask. The opposite occurs if the slider is moved towards 2 (Cells).</li>
		</ol>
		</li>
		<li>For cleanup, adjust the following as described below.
		<ol>
			<li>Hole Fill (&#181;m2): Adjust this to remove any hole in the cell body mask smaller than the area specified by the user.</li>
			<li>Adjust size (pixels): Increase (if positive) or shrink (if negative) the yellow mask by the specified number of pixels. It ranges from -10 to +10. Adjust this to add or remove yellow segmentation on the high contrast objects such as dead cells and cellular debris.</li>
			<li>Min cell width (&#181;m): Choose a value to define the size at which cell bodies will be considered as neurites.</li>
		</ol>
		</li>
		<li>For cell-body cluster filters, adjust the following as described below.
		<ol>
			<li>Area (&#181;m2): Set a minimum and a maximum value of cell body area. Values above and below the set values will not be considered as cell bodies.</li>
		</ol>
		</li>
		<li>For neurite parameters, adjust the following as described below.
		<ol>
			<li>Filtering: It reduces the masking of small vessel imperfections and debris. Choose between None, Better, and Best options. Choose None only for very clean cultures and vessels. Choose Better for faster processing at the expense of losing detection of very fine neurites. It may be sufficient for cells with thick or high-contrast neurites; also, it can be useful for vessels with many imperfections or debris. Choose Best for longer processing time, but it is the most sensitive filter setting to ensure the detection of very fine neurites.</li>
			<li>Neurite sensitivity: Use to adjust the detection sensitivity. Increase sensitivity to detect finer neurites. It ranges from 0.25 (Less) to 0.75 (More). 
			NOTE: It increases or decreases the software&#39;s sensitivity to recognize neurites. If the slider is moved towards 0.25 (Less), the software will be stricter in its recognition of neurites. Instead, if the slider is moved towards 0.75 (More), the software will be less strict in this detection, and therefore, more imperfections (i.e., cell debris, dirt) will be considered neurites.</li>
			<li>Neurite width (&#181;m): Use it to tune the detection to the size of the neurons. It can be 1, 2 or 4. By increasing it, the thinner neurites will not be considered. Set it to 1 for primary adult sensory neuron cultures and 2 for cell lines and embryonic sensory neuron cultures.</li>
		</ol>
		</li>
	</ol>
	</li>
	<li>Click Preview Current to visualize the segmented image. The following measurements will be provided for each image: Neurite Length (mm/mm2), Neurite Branch Points (Per mm2), Cell-Body Clusters (Per mm2), and Cell-Body Cluster Area (mm2/mm2).</li>
	<li>Repeat steps 2.3 and 2.4 for all the selected images. Click Next.</li>
	<li>Select the Scan time and well to analyze. Assign a Definition Name and, if needed, Analysis Notes. Click Next &#62; Finish.</li>
</ol>
3. Setup for immunocytochemistry (ICC) image analysis
<ol>
	<li>Follow the same steps illustrated from 2.1 to 2.4. Select the Image Channels for neurites and nuclei. Select the Set of images; select All images for each well to train the algorithm.</li>
	<li>Refine the Analysis Definition settings by adjusting the following parameters as described below. 
	NOTE: By default, neurites are segmented in blue, whereas cell bodies are purple. However, the colors can be modified as desired.
	<ol>
		<li>Cell-body cluster segmentation: Use this to segment the image into objects of interest. Estimate the background brightness at every pixel in the image. After the background is found, perform one of the following options.
		<ol>
			<li>No background subtraction: Use this to segment without altering the original picture. Choose between Adaptive or Fixed Threshold. Adaptive: the background is used to find objects but not explicitly subtracted; with this option, it is possible to set the Threshold Adjustment (GCU). Fixed Threshold: objects that are brighter than this threshold are detected in the original image; with this option, it is possible to set the Threshold (GCU).</li>
			<li>Background subtraction: Use this option to subtract the background from the image using a Top-Hat transform, then apply a threshold to it. With this option, set Radius and Threshold. Radius: a disk of this radius is used; the disk should be large enough that it does not fit entirely within any object in the image. Threshold: objects that are brighter than this threshold are detected in the background-subtracted image.</li>
		</ol>
		</li>
		<li>Cleanup: Use the following option to perform this.
		<ol>
			<li>Hole fill (&#181;m2): Use this to remove any holes in the cell body mask that are smaller than the area specified.</li>
			<li>Adjust size (pixels): Use this to increase (if positive) or shrink (if negative) the purple mask by the specified number of pixels. The range is -10 to +10. It adds or removes purple on high-contrast objects such as dead cells and cellular debris.</li>
			<li>Min cell width (&#181;m): Use this to define the size at which cell bodies will be considered as neurites.</li>
		</ol>
		</li>
		<li>Cell-body cluster filters: Use the following option to apply the filters.
		<ol>
			<li>Area (&#181;m2): Set a minimum and a maximum value of cell body area. Values above and below the set values will not be considered as cell bodies.</li>
		</ol>
		</li>
		<li>Neurite parameters: Use the following option to set these.
		<ol>
			<li>Neurite coarse sensitivity: Use this to adjust for neurite brightness. Sensitivity should be increased if the neurites&#39; fluorescence intensity is low. It ranges from 0 (Less) to 10 (More). It increases or decreases the sensitivity of the software to recognize less bright neurites. Optimal values range from 7 to 10; note that if it is set to 10, it is very likely that also background will be considered in the neurite measurement.</li>
			<li>Neurite fine sensitivity: Use this to adjust the detection sensitivity. Sensitivity should be increased to detect finer neurites. It ranges from 0.25 (Less) to 0.75 (More). It increases or decreases the sensitivity of the software to recognize fine and less bright neurites. If the slider is moved towards 0.25 (Less) the software will not consider faint neurites. Instead, if the slider is moved towards 0.75 (More) the software will detect also very faint (almost background) neurites.</li>
			<li>Neurite width (&#181;m): Use this to tune the detection to the size of the neurons. It can be 1, 2 or 4. By increasing it, the thinner neurites will not be considered. Set it on 1 for primary adult sensory neurons cultures, on 2 for cell lines and embryonic sensory neurons cultures.</li>
		</ol>
		</li>
	</ol>
	</li>
</ol>
4. Data export
<ol>
	<li>Open the analysis. Click on Graph Metrics.</li>
	<li>Select the Metric, Timepoints, and Wells of interest.</li>
	<li>Select the grouping option between All, None, Columns, Rows, and Plate Map Replicates.</li>
	<li>Click on Export Data and select the folder of destination and, if needed, other options. A .txt file will be created. 
	NOTE: The machine will provide a single average value of the chosen metric for each well. Manual annotation is required during the analysis to retrieve single image values.</li>
</ol>
5. Image export
<ol>
	<li>Open the vessel. Click on Export Images and Movies.</li>
	<li>Select the export type for the images.
	<ol>
		<li>Select As Displayed to export images as displayed. Click Next and select the Images of Interest for export. Click Next.
		<ol>
			<li>Select the Sequence Type between a Single Movie or Series of Images and the time points of interest. Click Next.</li>
			<li>Adjust the export options as needed and click Next. Set the output folder, file format, and name of the file, then click Export.</li>
		</ol>
		</li>
		<li>Select As Stored to export images in the raw format. Select the Image Type.
		<ol>
			<li>Select the Timepoints and Wells of interest. Click Next. Set the output folder, file format and name of the file, then click Export.</li>
		</ol>
		</li>
	</ol>
	</li>
	<li>Image export with the segmentation masks
	<ol>
		<li>Open the analysis. Click on the Icon of Image Layers. Select the Desired Channels Masks (Phase Neurite and Phase Cell-Body Cluster). Follow step 5.2.</li>
	</ol>
	</li>
</ol>

Advanced Live-Imaging Techniques for Accurate Neurite Outgrowth Measurement

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D., Gerhard, G. S. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Bile+acids+induce+neurite+outgrowth+in+NSC-34+cells+via+TGR5+and+a+distinct+transcriptional+profile.">Bile acids induce neurite outgrowth in NSC-34 cells via TGR5 and a distinct transcriptional profile.</a> Pharmaceuticals. 16, 174 (2023).</li><li>Tuttle, R., Matthew, W. D. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Neurotrophins+affect+the+pattern+of+DRG+neurite+growth+in+a+bioassay+that+presents+a+choice+of+CNS+and+PNS+substrates.">Neurotrophins affect the pattern of DRG neurite growth in a bioassay that presents a choice of CNS and PNS substrates.</a> Development. 121, 1301-1309 (1995).</li><li>Wurster, S., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Live+monitoring+and+analysis+of+fungal+growth,+viability,+and+mycelial+morphology+using+the+IncuCyte+NeuroTrack+processing+module.">Live monitoring and analysis of fungal growth, viability, and mycelial morphology using the IncuCyte NeuroTrack processing module.</a> mBio. 10 (3), e00673-e00619 (2019).</li></ol>

The authors declare that the research was conducted without any commercial or financial relationships that could potentially create a conflict of interest.

Accurately measuring how neurons grow in healthy, injured, and diseased conditions is a critical parameter in many experimental setups within the neuroscience field. Whether working with organotypic cultures of whole DRG explants or dissociated cultures, properly measuring axonal outgrowth has been a significant challenge over the last 20 years. Without reliable and accurate quantification of neurite outgrowth, it is impossible to assess if a specific treatment, such as retinoic acid (for 4 days) for NSC-34 cells34 or neurotrophins (for 1-2 days) for embryonic DRG neurons14,35, has been effective. Neurons typically exhibit continuous growth when healthy; however, following injury the axonal growth rate increases12,13. Timing is crucial when measuring axonal growth; therefore, before commencing an experiment, it is essential to conduct a trial test to determine the optimal time for fixing the cells based on their growth rate plateau curve.
The choice of the method, manual or automatic, marks a watershed in terms of time expenditure and accuracy. Some of the most common manual methods include NeuronJ18,20&#160;and Metamorph (Visitron)2,22,28. Manual methods require users to manually trace neurites, which is extremely time-consuming and requires single-cell images. With manual segmentation of neurites, neural networks are completely out of reach. Typically, these methodologies measure only the longest axon or use the vector distance measurement, thereby losing important information such as the number&#160;of branch points and the total axonal length. Somewhat of an improvement is provided by the Sholl analysis30, which anyway is limited to single-cell conditions. Single-cell analysis presents several challenges, starting with the seeding of cells. Neurons must be plated at a very low concentration, which may not be the most suitable growth condition for every cell type. Another issue arises from image acquisition. Usually, the confocal microscope is utilized for imaging, which requires trained users and fluorescent neurons and is neither time nor cost-efficient. With the confocal microscope high-resolution images are obtained, but very few neurons get imaged from each experiment. This represents a limitation as more biological replicates are necessary to reach an adequate number of neurons.
Some automatic methodologies such as NeuroMath2,28&#160;solve the issue of the time-consuming neurite segmentation which is performed in an automatic way.
However, due to time constraints, this neurite outgrowth measurement module provides faster results when acquiring images at the time-lapse microscopy machine. The latter, together with this software, significantly improves time and cost efficiency for both students and principal investigators.
The acquisition machine allows the creation of quite a complete map of the well, acquiring a variable number of images based on the diameter of the well. This represents a significant advantage as multiple neurons get imaged at the same time. However, reaching only a 20x magnification is sufficient and suitable to analyze the images with the software. Its power relies in its capability to train on a set of images and perform a semi-automatic measurement of the total axonal length. Additionally, the software can work on both single neurons and neuronal networks. The software is able to segment neurites and cell bodies with two different masks. A yellow mask segments all the high-contrast objects in the image, such as cell bodies, cell debris, and shadows. A magenta mask, instead, segments neurites. The precision and accuracy of the software were proven by the segmentation of the same neurons with both the software and NeuronJ. From the statistical analysis point of view, the values of neurite lengths nicely correlated with a high Spearman correlation coefficient.
After assessing the reliability of the method, we moved to the analysis of various test conditions. For an optimal analysis, some precautions are required. First, neurons have to be uniformly seeded in the well, avoiding spots with high cell concentration. The clustering of neurons causes the software to lose precision in the neurites&#39; detection. Another variable that influences the accuracy and precision of the analysis is the cleanliness of the culture. A clean culture with few cellular debris and dead cells is preferable. However, the software is able to compensate for such issues by modulation of the neurite sensitivity and the cell body segmentation mask. As aforementioned, the yellow mask segments high-contrast objects, among which there are also shadows caused by the movement of the medium in the well. The shadows might cover neurites, thereby resulting in the loss of neurite length. However, such an issue is easily resolved by allowing the medium to settle down before image acquisition.
The algorithm is able to perform neurite length quantification on both phase contrast images and immunocytochemistry images. When fluorescence is involved, other precautions have to be taken in order to obtain a reliable analysis. Firstly, the quality of the staining profoundly influences the outcome of the analysis. If neurites are broken or segmented and cell bodies are torn away during washes, the analysis loses strength and reliability. Additionally, the fluorescence itself represents a potentially disturbing element for the analysis. Since the focus is performed automatically by the machine, the objective puts on focus very bright objects such as artifacts, cell bodies, or thick neurites. As a result, thinner and less bright neurites are left behind, making it difficult for the user to properly measure the neurite length.
As a consequence, the analysis of phase images might be more well-founded compared to the analysis of immunocytochemistry images. The software is capable of working on many different neuronal morphologies from the most intricate and elaborate to the simplest ones, either as single-cells or in neuronal networks. Therefore, it is utilizable in many different research fields, ranging from primary cultures of neurons coming from the central or peripheral nervous system of various developmental stages to iPSC-derived neurons and cell lines such as NSC-34.
Despite the significant potential of the software, some limitations can be noted. Firstly, the precision of cell body segmentation is suboptimal. Consequently, parameters such as cell body cluster and cell body cluster area cannot be reliably used for cell counting. Secondly, in addition to the necessary precautions for optimal neurite segmentation, insufficiently thick axons may be excluded from the neurite length measurement, thereby resulting in data loss.
The branch point parameter encounters issues related to both types of segmentation. Shadows, dead cells, or debris in the culture that localize&#160;on branch points obscure them as they get covered by the cell body segmentation. Moreover, in the case of thin neurites, the reliability of the branch point parameter is again severely compromised.
Furthermore, the automatic focus during image acquisition can sometimes be suboptimal. The machine&#39;s maximal&#160;magnification is limited to 20x, which may be inadequate for observing finer details or fluorescence in slender structures such as neurites. Additionally, the machine performs best with homogeneous plastic substrates. If a glass coverslip is inserted in the well, the focus on the glass may fail, resulting in partially blurred images. However, this software not only applies to neurons but also to completely different fields of research, such as fungal growth36.
All things considered, we believe this neurite outgrowth measurement module to be a reliable tool for measuring neurites quickly, unbiasedly and efficiently.

In sciatic nerves, it is possible to measure axonal regeneration1. Additionally, in vitro studies have shown the feasibility of monitoring axonal outgrowth2,3 to comprehend its various phases, from axonal sprouting to axonal degeneration, in both healthy and injured neurons. By tracking these processes, it is possible to measure parameters such as axonal polarity, initiation, stability, and branching. The last parameter is crucial to understand neuropathic pain perception4,5,6. Similarly, axonal degeneration can be monitored in vivo7&#160;or in vitro8,9. During neurite outgrowth, actin and microtubule cytoskeletal networks stabilize or change according to the needs of the cell10. The actin cytoskeleton reorganizes to allow the formation of the axonal growth cone, and the microtubules re-align into bundles to stabilize the growing neurite11. In order to study neurite outgrowth of central and peripheral neurons in vitro, three common parameters are quantified: total axonal length, maximal distance, and branch points. These parameters are used to study the neuronal outgrowth response to treatment (i.e., neurotrophins, compounds, inhibitors, retinoic acid, siRNA, shRNA) or in genetically modified animals12,13,14. In order to assess if neurons have more elongated neurites and/or more branching, these three parameters allow us to assess the morphology of a neuron. Neurite length measurement is the top-interest parameter in several in vitro experimental setups. From dorsal root ganglia, mainly two types of cultures are performed: dissociated in vitro culture or organotypic culture of whole DRG explants. In either case, neurite length is a gold parameter to assess the outcome of the experiment. In a motor neuron-like cell line (NSC-34), axonal outgrowth and branching are measured after differentiation induced by retinoic acid15,16. In fact, by measuring the neurite outgrowth, it is possible to determine if a specific treatment has worked17, the growth rate18, or the regeneration capacity after an injury procedure19.
How to properly assess neurite outgrowth has posed a significant number of challenges over the years in the research field. However, there is no standardization of neurite length measurements. Some of the most utilized methods for in vitro cell cultures are, for example, the manual NeuronJ plug-in on Fiji18,20&#160;or MetaMorph21,23&#160;and the semi-automatic Neurolucida23,24. Other than manual methodologies, there are automatic methods, too, such as the NeuriteTracer plug-in on Fiji25, HCA Vision software26,27, or WIS-NeuroMath2,28. Other less accurate methodologies rely on the measurement of the overall dimension of the neurons. These methods include the measurement of the vector distance from the cell body to the tip of the longest axon29 or the Sholl analysis30. However, these measurement methods are suitable for very low-density cultures or single neurons. Moreover, all these methodologies are mainly utilized on stained neurons or neurons that are expressing genetically encoded fluorophores (i.e., GFP, Venus, mCherry). The type of neuron and the density of the cell culture deeply affect the choice of measurement methodology. For example, manually segmenting neurons with very intricate and complicated morphologies, such as DRG neurons, can easily become an impossible task. If convoluted neurons are already a challenge to segment, neural nets are completely out of reach for manual approaches due to their highly complex organization.
On the one hand, manual segmentation is very precise because it is performed by human eyes and intelligence; on the other hand, it is really time-consuming. The elevated time expenditure required by manual methods is the main drawback. For this reason, only a few neurons are acquired for analysis, making it less accurate and costly in terms of time. Automatic or semi-automatic approaches, on the other hand, partially reduce the time expenditure. However, they also have some disadvantages. Automatic methods need to be trained in order to work properly, and if the software is not interactive enough with the user, the segmentation can be wrong.
Other than neurite outgrowth measurement, the number of branch points is also valuable information. With manual segmentation, the number of branch points can be calculated, whereas this is not possible with a vector distance. With automatic methods, the number of branch points is usually provided, whereas with the Sholl analysis, it has to be calculated with a mathematical formula.
In this methods paper, we aim to describe the functionality and effectiveness of this semi-automatic software in measuring the total axonal length and other parameters. The machine allows for the automatic acquisition of images at defined time points or for conducting long-term studies (days, weeks, months), preserving a physiological environment for live cells. Measuring neurite outgrowth using phase-contrast time-lapse imaging has the benefit of enabling continuous monitoring of neurite kinetics and growth. Additionally, it is also possible to monitor cell death through the addition in the media of specific dyes that target dead cells31,32,33. Although the software has been released in 2012, we are the first to standardize this methodology in a reproducible and unbiased way for the accurate quantification of neurite outgrowth. However, it is important to note that the software is not included with the purchase of the machine. Despite this additional expense, its use offers significant advantages in measuring total axonal length and other parameters, thereby contributing to research in the field of neuroscience.

<table border="1" fo:keep-together.within-page="1" fo:keep-with-next.within-page="always">
	<tbody>
		<tr>
			<td>Collagenase A</td>
			<td>Merck / Roche</td>
			<td>10103586001</td>
			<td></td>
		</tr>
		<tr>
			<td>Dispase II (neutral protease, grade II)</td>
			<td>Merck / Roche</td>
			<td>4942078001</td>
			<td></td>
		</tr>
		<tr>
			<td>Dulbecco&#39;s modified eagle&#39;s medium</td>
			<td>Merck / Sigma</td>
			<td>D5796</td>
			<td></td>
		</tr>
		<tr>
			<td>Fetal bovin serum&#160;</td>
			<td>Merck / Sigma</td>
			<td>F7524</td>
			<td></td>
		</tr>
		<tr>
			<td>Ham&#39;s F-12 Nutrient Mix (1X)</td>
			<td>ThermoFisher Scientific</td>
			<td>21765029</td>
			<td></td>
		</tr>
		<tr>
			<td>Ham&#39;s F12 w/ L-Glutamine</td>
			<td>Euroclone</td>
			<td>ECM0135L</td>
			<td></td>
		</tr>
		<tr>
			<td>Hanks&#39; Balanced Salt Solution</td>
			<td>Euroclone</td>
			<td>ECM0507L</td>
			<td></td>
		</tr>
		<tr>
			<td>HBSS (10X), no calcium, no magnesium, no phenol red</td>
			<td>ThermoFisher Scientific</td>
			<td>14185045</td>
			<td></td>
		</tr>
		<tr>
			<td>HyClone Characterized Fetal Bovine Serum (U.S.)</td>
			<td>Cytiva</td>
			<td>SH30071.03</td>
			<td></td>
		</tr>
		<tr>
			<td>Incucyte, Neurotrack Analysis Software&#160;</td>
			<td>Sartorius</td>
			<td>9600-0010</td>
			<td></td>
		</tr>
		<tr>
			<td>L-15 Medium (Leibovitz)</td>
			<td>Millipore/Sigma</td>
			<td>L5520</td>
			<td></td>
		</tr>
		<tr>
			<td>Laminin Mouse Protein, Natural</td>
			<td>ThermoFisher Scientific</td>
			<td>23017015</td>
			<td></td>
		</tr>
		<tr>
			<td>L-Cysteine</td>
			<td>Merck / Sigma</td>
			<td>C7352</td>
			<td></td>
		</tr>
		<tr>
			<td>Leibovitz&#39;s L-15 medium w/o L-glutamine</td>
			<td>Euroclone</td>
			<td>ECB0020L</td>
			<td></td>
		</tr>
		<tr>
			<td>mouse NGF 2.5S (&#62;95%)</td>
			<td>Alomone Labs</td>
			<td>N-100</td>
			<td></td>
		</tr>
		<tr>
			<td>Neurobasal Medium [-] Glutamine</td>
			<td>ThermoFisher Scientific</td>
			<td>21103049</td>
			<td></td>
		</tr>
		<tr>
			<td>NSC-34</td>
			<td>CELLutions Biosystems Inc (Ontario, Canada)</td>
			<td>CLU140</td>
			<td></td>
		</tr>
		<tr>
			<td>Papain from papaya latex</td>
			<td>Sigma</td>
			<td>P4762</td>
			<td></td>
		</tr>
		<tr>
			<td>Penicillin-Streptomycin (5,000 U/mL)</td>
			<td>ThermoFisher Scientific</td>
			<td>15070063</td>
			<td></td>
		</tr>
		<tr>
			<td>Percoll (Density 1.130 g/mL)</td>
			<td>Cytiva</td>
			<td>17089101</td>
			<td></td>
		</tr>
		<tr>
			<td>Poly-D-Lysine Solution (1mg/mL)</td>
			<td>EMD Millipore/Merck</td>
			<td>A-003-E</td>
			<td></td>
		</tr>
		<tr>
			<td>Poly-L-Lysine Solution (0-01%)</td>
			<td>Sigma</td>
			<td>P4832</td>
			<td></td>
		</tr>
		<tr>
			<td>Recombinant Human NT-3</td>
			<td>PeproTech</td>
			<td>450-03</td>
			<td></td>
		</tr>
		<tr>
			<td>Retinoic Acid</td>
			<td>Merck / Sigma</td>
			<td>R2625</td>
			<td></td>
		</tr>
		<tr>
			<td>Trypsin-EDTA solution</td>
			<td>Sigma</td>
			<td>T3924</td>
			<td></td>
		</tr>
		<tr>
			<td>&#946;-Tubulin III (Tuj1) antibody</td>
			<td>Merck / Sigma</td>
			<td>T8660</td>
			<td></td>
		</tr>
	</tbody>
</table>

standardization of a novel semi-automatic software for neurite outgrowth measurement

Effective live-imaging techniques are crucial to assess neuronal morphology in order to measure neurite outgrowth in real time. The proper measurement of neurite outgrowth has been a long-standing challenge over the years in the neuroscience research field. This parameter serves as a cornerstone in numerous in vitro experimental setups, ranging from dissociated cultures and organotypic cultures to cell lines. By quantifying the neurite length, it is possible to determine if a specific treatment worked or if axonal regeneration is enhanced in different experimental groups. In this study, the aim is to demonstrate the robustness and accuracy of the Incucyte Neurotrack neurite outgrowth analysis software. This semi-automatic software is available in a time-lapse microscopy system which offers several advantages over commonly used methodologies in the quantification of the neurite length in phase contrast images. The algorithm masks and quantifies several parameters in each image and returns neuronal cell metrics, including neurite length, branch points, cell-body clusters, and cell-body cluster areas. Firstly, we validated the robustness and accuracy of the software by correlating its values with those of the manual NeuronJ, a Fiji plug-in. Secondly, we used the algorithm which is able to work both on phase contrast images as well as on immunocytochemistry images. Using specific neuronal markers, we validated the feasibility of the fluorescence-based neurite outgrowth analysis on sensory neurons in vitro cultures. Additionally, this software can measure neurite length across various seeding conditions, ranging from individual cells to complex neuronal nets. In conclusion, the software provides an innovative and time-effective platform for neurite outgrowth assays, paving the way for faster and more reliable quantifications.

Author Spotlight: Unveiling the Molecular Basis of Pain Perception and Neuropathic Pain

Neurite outgrowth assays provide a quantitative value about regenerative neuronal processes. The advantage of this semi-automatic software is that it segments cell bodies and neurites separately by creating a mask and measures various parameters such as neurite length, number of branch points, cell-body cluster area, and number of cell clusters.

Standardization of a Novel Semi-Automatic Software for Neurite Outgrowth Measurement

Effective live-imaging techniques are crucial to assess neuronal morphology in order to measure neurite outgrowth in real time. The proper measurement of ...

standardization-novel-semi-automatic-software-for-neurite-outgrowth

Research

JoVE Journal

Neuroscience

877 Views.  University of Turin. Neurite outgrowth assays provide a quantitative value about regenerative neuronal processes. The advantage of this semi-automatic software is that it segments cell bodies and neurites separately by creating a mask and measures various parameters such as neurite length, number of branch points, cell-body cluster area, and number of cell clusters.

Video: Author Spotlight: Unveiling the Molecular Basis of Pain Perception and Neuropathic Pain

Cerebral Blood Oxygenation Measurement Based on Oxygen-dependent Quenching of Phosphorescence

Monitoring of the spatiotemporal characteristics of cerebral blood and tissue oxygenation is crucial for better understanding of the 
neuro-metabolic-vascular relationship. Development of new pO2 measurement modalities with simultaneous monitoring of pO2 in larger fields of view with higher 
spatial and/or temporal resolution will enable greater insight into the functioning of the normal brain and will also have significant impact on diagnosis 
and treatment of neurovascular diseases such as stroke, Alzheimer's disease, and head injury.
Optical imaging modalities have shown a great potential to provide high spatiotemporal resolution and quantitative imaging of pO2 based on hemoglobin absorption in visible and near infrared range of optical spectrum. However, multispectral measurement of cerebral blood oxygenation relies on photon migration through the highly scattering brain tissue. Estimation and modeling of tissue optical parameters, which may undergo dynamic changes during the experiment, is typically required for accurate estimation of blood oxygenation. On the other hand, estimation of the partial pressure of oxygen (pO2) based on oxygen-dependent quenching of phosphorescence should not be significantly affected by the changes in the optical parameters of the tissue and provides an absolute measure of pO2. Experimental systems that utilize oxygen-sensitive dyes have been demonstrated in in vivo studies of the perfused tissue as well as for monitoring the oxygen content in tissue cultures, showing that phosphorescence quenching is a potent technology capable of accurate oxygen imaging in the physiological pO2 range. 
Here we demonstrate with two different imaging modalities how to perform measurement of pO2 in cortical vasculature based on phosphorescence lifetime imaging. In first demonstration we present wide field of view imaging of pO2 at the cortical surface of a rat. This imaging modality has relatively simple experimental setup based on a CCD camera and a pulsed green laser. An example of monitoring the cortical spreading depression based on phosphorescence lifetime of Oxyphor R3 dye was presented. In second demonstration we present a high resolution two-photon pO2 imaging in cortical micro vasculature of a mouse. The experimental setup includes a custom built 2-photon microscope with femtosecond laser, electro-optic modulator, and photon-counting photo multiplier tube. We present an example of imaging the pO2 heterogeneity in the cortical microvasculature including capillaries, using a novel PtP-C343 dye with enhanced 2-photon excitation cross section.
Click here to view the related article <a href="http://www.jove.com/Details.php?ID=1731">Synthesis and Calibration of Phosphorescent Nanoprobes for Oxygen Imaging in Biological Systems.</a>

We present an experimental procedure for measuring the partial pressure of oxygen (pO2) in cerebral vasculature based on oxygen-dependent quenching of phosphorescence. Animal preparation and imaging procedures were outlined for both large field of view CCD-based imaging of pO2 in rats and 2-photon excitation based imaging of pO2 in mice.

Monitoring of the spatiotemporal characteristics of cerebral blood and tissue oxygenation is crucial for better understanding of the 
...

A Novel Approach for Documenting Phosphenes Induced by Transcranial Magnetic Stimulation

Stimulation of the human visual cortex produces a transient perception of light, known as a phosphene. Phosphenes are induced by invasive electrical stimulation of the occipital cortex, but also by non-invasive Transcranial Magnetic Stimulation (TMS)1 of the same cortical regions. The intensity at which a phosphene is induced (phosphene threshold) is a well established measure of visual cortical excitability and is used to study cortico-cortical interactions, functional organization 2, susceptibility to pathology 3,4 and visual processing 5-7. Phosphenes are typically defined by three characteristics: they are observed in the visual hemifield contralateral to stimulation; they are induced when the subject s eyes are open or closed, and their spatial location changes with the direction of gaze 2. Various methods have been used to document phosphenes, but a standardized methodology is lacking. We demonstrate a reliable procedure to obtain phosphene threshold values and introduce a novel system for the documentation and analysis of phosphenes. We developed the Laser Tracking and Painting system (LTaP), a low cost, easily built and operated system that records the location and size of perceived phosphenes in real-time. The LTaP system provides a stable and customizable environment for quantification and analysis of phosphenes.

Phosphenes are transient percepts of light that can be induced by applying Transcranial Magnetic Stimulation (TMS) to visually sensitive regions of cortex. We demonstrate a standard protocol for determining the phosphene threshold value and introduce a novel method for quantifying and analyzing perceived phosphenes.

Stimulation of the human visual cortex produces a transient perception of light, known as a phosphene. Phosphenes are induced by invasive electrical ...

Novel Apparatus and Method for Drug Reinforcement

Animal models of reinforcement have proven to be useful for understanding the neurobiological mechanisms underlying drug addiction. Operant drug self-administration and conditioned place preference (CPP) procedures are expansively used in animal research to model various components of drug reinforcement, consumption, and addiction in humans. For this study, we used a novel approach to studying drug reinforcement in rats by combining traditional CPP and self-administration methodologies. We assembled an apparatus using two Med Associate operant chambers, sensory stimuli, and a Plexiglas-constructed neutral zone. These modifications allowed our experiments to encompass motivational aspects of drug intake through self-administration and drug-free assessment of drug/cue conditioning strength with the CPP test. In our experiments, rats self-administered cocaine (0.75 mg/kg/inj, i.v.) during either four (e.g., the "short-term") or eight (e.g., the "long-term") alternating-day sessions in an operant environment containing distinctive sensory cues (e.g., olfactory and visual). On the alternate days, in the other (differently-cued) operant environment, saline was available for self-infusion (0.1 ml, i.v.). Twenty-four hours after the last self-administration/cue-pairing session, a CPP test was conducted. Consistent with typical CPP findings, there was a significant preference for the chamber associated with cocaine self-administration. In addition, in animals undergoing the long-term experiment, a significant positive correlation between CPP magnitude and the number of cocaine-reinforced lever responses. In conclusion, this apparatus and approach is time and cost effective, can be used to examine a wide array of topics pertaining to drug abuse, and provides more flexibility in experimental design than CPP or self-administration methods alone.

Operant drug self-administration and conditioned place preference (CPP) procedures are expansively used in research to model various components of drug reinforcement, consumption, and addiction in humans. In this report, we combined traditional CPP and self-administration methods as a novel approach to studying drug reinforcement and addiction in rats.

Animal models of reinforcement have proven to be useful for understanding the neurobiological mechanisms underlying drug addiction.  Operant drug ...

Organotypic Slice Culture of GFP-expressing Mouse Embryos for Real-time Imaging of Peripheral Nerve Outgrowth

For many purposes, the cultivation of mouse embryos ex vivo as organotypic slices is desirable. For example, we employ a transgenic mouse line (tauGFP) in which the enhanced version of the green fluorescent protein (EGFP) is exclusively expressed in all neurons of the developing central and peripheral nervous system1, allowing the possibility to both film the innervation of the forelimb and to manipulate this process with pharmacological and genetic techniques2. The most critical parameter in the successful cultivation of such slice cultures is the method by which the slices are prepared. After extensive testing of a variety of methods, we have found that a vibratome is the best possible device to slice the embryos such that they routinely result in a culture that demonstrates viability over a period of several days, and most importantly, develops in an age-specific manner. For mid-gestation embryos, this includes the normal outgrowth of spinal nerves from the spinal cord and the dorsal root ganglia to their targets in the periphery and the proper determination of skeletal and muscle tissue. 
In this work, we present a method for processing whole embryos of embryonic day (E) E10 to E12 into 300 - 400 micrometer slices for cultivation in a standard tissue culture incubator, which can be studied for up to two days after slice preparation. Critical for the success of this approach is the use of a vibratome to slice each agarose-embedded embryo. This is followed by the cultivation of the slices upon Millicell culture membrane inserts placed upon a small volume of medium, resulting in an interface culture technique. One litter with an average of 7 embryos routinely produces at least 14 slices (2-3 slices of the forelimb region per embryo), which varies slightly due to the age of the embryos as well as to the thickness of the slices. About 80% of the cultured slices show nerve outgrowth, which can be measured througout the culturing period2. Representative results using the tauGFP mouse line are demonstrated.

We present a method to prepare organotypic slices of mid-gestation mouse embryos for the cultivation and time-lapse imaging of peripheral nerve outgrowth.

For many purposes, the cultivation of mouse embryos ex vivo as organotypic slices is desirable. For example, we employ a transgenic mouse line (tauGFP) in ...

VisualEyes: A Modular Software System for Oculomotor Experimentation

Eye movement studies have provided a strong foundation forming an understanding of how the brain acquires visual information in both the normal and dysfunctional brain.1 However, development of a platform to stimulate and store eye movements can require substantial programming, time and costs. Many systems do not offer the flexibility to program numerous stimuli for a variety of experimental needs. However, the VisualEyes System has a flexible architecture, allowing the operator to choose any background and foreground stimulus, program one or two screens for tandem or opposing eye movements and stimulate the left and right eye independently. This system can significantly reduce the programming development time needed to conduct an oculomotor study. The VisualEyes System will be discussed in three parts: 1) the oculomotor recording device to acquire eye movement responses, 2) the VisualEyes software written in LabView, to generate an array of stimuli and store responses as text files and 3) offline data analysis. Eye movements can be recorded by several types of instrumentation such as: a limbus tracking system, a sclera search coil, or a video image system. Typical eye movement stimuli such as saccadic steps, vergent ramps and vergent steps with the corresponding responses will be shown. In this video report, we demonstrate the flexibility of a system to create numerous visual stimuli and record eye movements that can be utilized by basic scientists and clinicians to study healthy as well as clinical populations.

Neural control and cognitive processes can be studied through eye movements. The VisualEyes software allows an operator to program stimuli on two computer screens independently using a simple, custom scripting language. The system can stimulate tandem eye movements (saccades and smooth pursuit) or opposing eye movements (vergence) or any combination.

Eye movement studies have provided a strong foundation forming an understanding of how the brain acquires visual information in both the normal and ...

Dissection and Culture of Chick Statoacoustic Ganglion and Spinal Cord Explants in Collagen Gels for Neurite Outgrowth Assays

The sensory organs of the chicken inner ear are innervated by the peripheral processes of statoacoustic ganglion (SAG) neurons. Sensory organ innervation depends on a combination of axon guidance cues1 and survival factors2 located along the trajectory of growing axons and/or within their sensory organ targets. For example, functional interference with a classic axon guidance signaling pathway, semaphorin-neuropilin, generated misrouting of otic axons3. Also, several growth factors expressed in the sensory targets of the inner ear, including Neurotrophin-3 (NT-3) and Brain Derived Neurotrophic Factor (BDNF), have been manipulated in transgenic animals, again leading to misrouting of SAG axons4. These same molecules promote both survival and neurite outgrowth of chick SAG neurons in vitro5,6.
Here, we describe and demonstrate the in vitro method we are currently using to test the responsiveness of chick SAG neurites to soluble proteins, including known morphogens such as the Wnts, as well as growth factors that are important for promoting SAG neurite outgrowth and neuron survival. Using this model system, we hope to draw conclusions about the effects that secreted ligands can exert on SAG neuron survival and neurite outgrowth. 
SAG explants are dissected on embryonic day 4 (E4) and cultured in three-dimensional collagen gels under serum-free conditions for 24 hours. First, neurite responsiveness is tested by culturing explants with protein-supplemented medium. Then, to ask whether point sources of secreted ligands can have directional effects on neurite outgrowth, explants are co-cultured with protein-coated beads and assayed for the ability of the bead to locally promote or inhibit outgrowth. We also include a demonstration of the dissection (modified protocol7) and culture of E6 spinal cord explants. We routinely use spinal cord explants to confirm bioactivity of the proteins and protein-soaked beads, and to verify species cross-reactivity with chick tissue, under the same culture conditions as SAG explants. These in vitro assays are convenient for quickly screening for molecules that exert trophic (survival) or tropic (directional) effects on SAG neurons, especially before performing studies in vivo. Moreover, this method permits the testing of individual molecules under serum-free conditions, with high neuron survival8.

We demonstrate how to dissect and culture chick E4 statoacoustic ganglion and E6 spinal cord explants. Explants are cultured under serum-free conditions in 3D collagen gels for 24 hours. Neurite responsiveness is tested with growth factor-supplemented medium and with protein-coated beads.

The sensory organs of the chicken inner ear are innervated by the peripheral processes of statoacoustic ganglion (SAG) neurons. Sensory organ innervation ...

A High Content Imaging Assay for Identification of Botulinum Neurotoxin Inhibitors

Synaptosomal-associated protein-25 (SNAP-25) is a component of the soluble NSF attachment protein receptor (SNARE) complex that is essential for synaptic neurotransmitter release. Botulinum neurotoxin serotype A (BoNT/A) is a zinc metalloprotease that blocks exocytosis of neurotransmitter by cleaving the SNAP-25 component of the SNARE complex. Currently there are no licensed medicines to treat BoNT/A poisoning after internalization of the toxin by motor neurons. The development of effective therapeutic measures to counter BoNT/A intoxication has been limited, due in part to the lack of robust high-throughput assays for screening small molecule libraries. Here we describe a high content imaging (HCI) assay with utility for identification of BoNT/A inhibitors. Initial optimization efforts focused on improving the reproducibility of inter-plate results across multiple, independent experiments. Automation of immunostaining, image acquisition, and image analysis were found to increase assay consistency and minimize variability while enabling the multiparameter evaluation of experimental compounds in a murine motor neuron system.

Botulinum neurotoxin is one of the most potent toxins among Category-A biothreat agents, yet a post-exposure therapeutic is not available. The high content imaging approach is a powerful methodology for identifying novel inhibitors as it enables multiparameter screening using biologically relevant motor neurons, the primary target of this toxin.

Synaptosomal-associated protein-25 (SNAP-25) is a component of the soluble NSF attachment protein receptor (SNARE) complex that is essential for synaptic ...

Novel Assay for Cold Nociception in Drosophila Larvae

How organisms sense and respond to noxious temperatures is still poorly understood. Further, the mechanisms underlying sensitization of the sensory machinery, such as in patients experiencing peripheral neuropathy or injury-induced sensitization, are not well characterized. The genetically tractable Drosophila model has been used to study the cells and genes required for noxious heat detection, which has yielded multiple conserved genes of interest. Little is known however about the cells and receptors important for noxious cold sensing. Although, Drosophila does not survive prolonged exposure to cold temperatures (&#8804;10 &#186;C), and will avoid cool, preferring warmer temperatures in behavioral preference assays, how they sense and possibly avoid noxious cold stimuli has only recently been investigated.
Here we describe and characterize the first noxious cold (&#8804;10 &#186;C) behavioral assay in Drosophila. Using this tool and assay, we show an investigator how to qualitatively and quantitatively assess cold nociceptive behaviors. This can be done under normal/healthy culture conditions, or presumably in the context of disease, injury or sensitization. Further, this assay can be applied to larvae selected for desired genotypes, which might impact thermosensation, pain, or nociceptive sensitization. Given that pain is a highly conserved process, using this assay to further study&#160;thermal nociception will likely glean important understanding of pain processes in other species, including vertebrates.

Novel Assay for Cold Nociception in Drosophila Larvae

Here we demonstrate a novel assay to study cold nociception in Drosophila larvae. This assay utilizes a custom-built Peltier probe capable of applying a focal noxious cold stimulus and results in quantifiable cold-specific behaviors. This technique will allow further cellular and molecular dissection of cold nociception.

How organisms sense and respond to noxious temperatures is still poorly understood. Further, the mechanisms underlying sensitization of the sensory ...

Rewiring Neuronal Circuits: A New Method for Fast Neurite Extension and Functional Neuronal Connection

Brain and spinal cord injury may lead to permanent disability and death because it is still not possible to regenerate neurons over long distances and accurately reconnect them with an appropriate target. Here a procedure is described to rapidly initiate, elongate, and precisely connect new functional neuronal circuits over long distances. The extension rates achieved reach over 1.2 mm/h, 30-60 times faster than the in vivo rates of the fastest growing axons from the peripheral nervous system (0.02 to 0.04 mm/h)28 and 10 times faster than previously reported for the same neuronal type at an earlier stage of development4. First, isolated populations of rat hippocampal neurons are grown for 2-3 weeks in microfluidic devices to precisely position the cells, enabling easy micromanipulation and experimental reproducibility. Next, beads coated with poly-D-lysine (PDL) are placed on neurites to form adhesive contacts and pipette micromanipulation is used to move the resulting bead-neurite complex. As the bead is moved, it pulls out a new neurite that can be extended over hundreds of micrometers and functionally connected to a target cell in less than 1 h. This process enables experimental reproducibility and ease of manipulation while bypassing slower chemical strategies to induce neurite growth. Preliminary measurements presented here demonstrate a neuronal growth rate far exceeding physiological ones. Combining these innovations allows for the precise establishment of neuronal networks in culture with an unprecedented degree of control. It is a novel method that opens the door to a plethora of information and insights into signal transmission and communication within the neuronal network as well as being a playground in which to explore the limits of neuronal growth. The potential applications and experiments are widespread with direct implications for therapies that aim to reconnect neuronal circuits after trauma or in neurodegenerative diseases.

This procedure describes how to rapidly initiate, extend and connect neurites organized in microfluidic chambers using poly-D-lysine-coated beads fixed to micropipettes that guide neurite elongation.

Brain and spinal cord injury may lead to permanent disability and death because it is still not possible to regenerate neurons over long distances and ...

Assay Development for High Content Quantification of Sod1 Mutant Protein Aggregate Formation in Living Cells

Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disease that can be caused by inherited mutations in the gene encoding copper-zinc superoxide dismutase 1 (SOD1). The structural instability of SOD1 and the detection of SOD1-positive inclusions in familial-ALS patients supports a potential causal role for misfolded and/or aggregated SOD1 in ALS pathology. In this study, we describe the development of a cell-based assay designed to quantify the dynamics of SOD1 aggregation in living cells by high content screening approaches. Using lentiviral vectors, we generated stable cell lines expressing wild-type and mutant A4V SOD1 tagged with yellow fluorescent protein and found that both proteins were expressed in the cytosol without any sign of aggregation. Interestingly, only SOD1 A4V stably expressed in HEK-293, but not in U2OS or SH-SY5Y cell lines, formed aggregates upon proteasome inhibitor treatment. We show that it is possible to quantify aggregation based on dose-response analysis of various proteasome inhibitors, and to track aggregate-formation kinetics by time-lapse microscopy. Our approach introduces the possibility of quantifying the effect of ALS mutations on the role of SOD1 in aggregate formation as well as screening for small molecules that prevent SOD1 A4V aggregation.

We describe a method to quantify the aggregation of misfolded proteins. Our protocol details lentiviral induced stable cell line generation, automated confocal imaging, and image analysis of protein aggregates. As an illustrative application, we studied the effect of small molecules in promoting SOD1 aggregation in a time- and dose-dependent manner.

Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disease that can be caused by inherited mutations in the gene encoding copper-zinc ...