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In This Article

  • Summary
  • Abstract
  • Introduction
  • Protocol
  • Representative Results
  • Discussion
  • Acknowledgements
  • Materials
  • References
  • Reprints and Permissions

Summary

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.

Abstract

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.

Introduction

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. Similar....

Protocol

1. Scanning the vessel on the machine

NOTE: The detection is performed by the built-in Basler Ace 1920-155 µm camera.

  1. Open the program by clicking Connect to Device and selecting Schedule - To Acquire. Then click the + sign.
  2. Specify whether the vessel will be scanned repeatedly or only 1x by choosing the option Scan on Schedule or Scan Once Now, respectively.
  3. <.......

Representative Results

The neurite outgrowth measurement algorithm is robustly capable of detecting neurites in both neural networks and single neurons. It generates a yellow mask that segments objects with high contrast, such as cell bodies, cellular debris, dead cells, tissue explants, and shadows. Additionally, a magenta mask appears on neurites of various thicknesses. Neurite length values are provided in mm/mm2, indicating that the axonal length has been divided by the area of the image, which is 0.282739 mm2 and con.......

Discussion

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 cells

Acknowledgements

We want to thank Alessandro Vercelli for the critical comments and Sartorius'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'Istruzione dell'Università e della Ricerca MIUR project Dipartimenti di Eccellenza 2023-2027 to Department of Neuroscience Rita Levi Montalcini. D.M.R.'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).

....

Materials

NameCompanyCatalog NumberComments
Collagenase AMerck / Roche10103586001
Dispase II (neutral protease, grade II)Merck / Roche4942078001
Dulbecco's modified eagle's mediumMerck / SigmaD5796
Fetal bovin serum Merck / SigmaF7524
Ham's F-12 Nutrient Mix (1X)ThermoFisher Scientific21765029
Ham's F12 w/ L-GlutamineEurocloneECM0135L
Hanks' Balanced Salt SolutionEurocloneECM0507L
HBSS (10X), no calcium, no magnesium, no phenol redThermoFisher Scientific14185045
HyClone Characterized Fetal Bovine Serum (U.S.)CytivaSH30071.03
Incucyte, Neurotrack Analysis Software Sartorius9600-0010
L-15 Medium (Leibovitz)Millipore/SigmaL5520
Laminin Mouse Protein, NaturalThermoFisher Scientific23017015
L-CysteineMerck / SigmaC7352
Leibovitz's L-15 medium w/o L-glutamineEurocloneECB0020L
mouse NGF 2.5S (>95%)Alomone LabsN-100
Neurobasal Medium [-] GlutamineThermoFisher Scientific21103049
NSC-34CELLutions Biosystems Inc (Ontario, Canada)CLU140
Papain from papaya latexSigmaP4762
Penicillin-Streptomycin (5,000 U/mL)ThermoFisher Scientific15070063
Percoll (Density 1.130 g/mL)Cytiva17089101
Poly-D-Lysine Solution (1mg/mL)EMD Millipore/MerckA-003-E
Poly-L-Lysine Solution (0-01%)SigmaP4832
Recombinant Human NT-3PeproTech450-03
Retinoic AcidMerck / SigmaR2625
Trypsin-EDTA solutionSigmaT3924
β-Tubulin III (Tuj1) antibodyMerck / SigmaT8660

References

  1. Terenzio, M., et al. Locally translated mTOR controls axonal local translation in nerve injury. Science. 359, 1416-1421 (2018).
  2. Marvaldi, L., et al. Enhanced axon outgrowth and improv....

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