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In This Article

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

Summary

This protocol describes a microglia-neuronal co-culture established from primary neuronal cells isolated from mouse embryos at embryonic days 15-16 and primary microglia generated from the brains of neonatal mice at post-natal days 1-2.

Abstract

Microglia are tissue-resident macrophages of the central nervous system (CNS), performing numerous functions that support neuronal health and CNS homeostasis. They are a major population of immune cells associated with CNS disease activity, adopting reactive phenotypes that potentially contribute to neuronal injury during chronic neurodegenerative diseases such as multiple sclerosis (MS). The distinct mechanisms by which microglia regulate neuronal function and survival during health and disease remain limited due to challenges in resolving the complex in vivo interactions between microglia, neurons, and other CNS environmental factors. Thus, the in vitro approach of co-culturing microglia and neurons remains a valuable tool for studying microglia-neuronal interactions. Here, we present a protocol to generate and co-culture primary microglia and neurons from mice. Specifically, microglia were isolated after 9-10 days in vitro from a mixed glia culture established from brain homogenates derived from neonatal mice between post-natal days 0-2. Neuronal cells were isolated from brain cortices of mouse embryos between embryonic days 16-18. After 4-5 days in vitro, neuronal cells were seeded in 96-well plates, followed by the addition of microglia to form the co-culture. Careful timing is critical for this protocol as both cell types need to reach experimental maturity to establish the co-culture. Overall, this co-culture can be useful for studying microglia-neuron interactions and can provide multiple readouts, including immunofluorescence microscopy, live imaging, as well as RNA and protein assays.

Introduction

Microglia are tissue-resident macrophages that facilitate immunosurveillance and homeostasis in the central nervous system (CNS)1,2,3. They originate from yolk sac erythromyeloid progenitor cells that colonize the brain during embryonic development4,5,6 and are maintained throughout the organism's life span through self-renewal, which involves proliferation and apoptosis7. At steady-state, resting microglia have ramified morphology and engage in tissu....

Protocol

All animals used in this study were housed and handled with approval from the University Animal Care Committee (UACC) of the University of Saskatchewan and the Canadian Council on Animal Care (CCAC). Post-natal days 0-2 CD1 male and female mice and embryonic days 16-18 (E16-18) embryos from pregnant CD1 mice were used for this study. The details of the reagents and the equipment used are listed in the Table of Materials.

1. Primary microglia culture

Representative Results

A flowchart showing the key steps of the mixed glia culture for microglia is shown in Figure 1A. Overall, sparse cells and excessive cellular debris are expected on day 1 (Figure 1B). By day 4, increased cell number should be observed, especially with the generation of adherent astrocytes, as indicated by their elongated morphology (Figure 1C). A few microglia may be observed on top of the astrocytes or as small round cells flo.......

Discussion

This article describes a protocol for isolating and culturing mouse primary neurons and primary microglia, which are subsequently used to establish a microglia-neuronal co-culture that can be used to study how microglia and neuron interactions regulate their cellular health and function. This relatively simple and accessible approach can provide critical insights into the mechanisms and functional outcomes of microglia neuron interactions in the CNS.

To achieve an optimal co-culture, several c.......

Acknowledgements

JP acknowledges funding support from the Natural Sciences and Engineering Research Council of Canada and the University of Saskatchewan College of Medicine. YD acknowledges funding support from the University of Saskatchewan College of Medicine Startup Fund, the Natural Sciences and Engineering Research Council of Canada Discovery Grant (RGPIN-2023-03659), MS Canada Catalyst Grant (1019973), Saskatchewan Health Research Foundation Establishment Grant (6368), and Brain Canada Foundation Future Leaders in Canadian Brain Research Grant. Figure 1A, Figure 2A, and Figure 3A were created with BioRender.com.

....

Materials

NameCompanyCatalog NumberComments
10 cm Petri dish Fisher 07-202-011Sterile
1x VerseneGibco15040-066
B-27 Plus Neuronal Culture System Gibco A3653401
Dissection microscopeVWR
DNase IRoche11284932001
Dulbecco’s Modified Eagle Medium (DMEM)Gibco11960-044
Fetal Bovine Serum ThermoFisher Sci12483-020
HBSS (10x)Gibco14065-056
HemacytometerHausser Scientific1475
HEPES ThermoFisher Sci15630080
Leibovitz’s L-15 Medium (1x)Fisher Scientific 21083027
Macrophage colony stimulating factor Peprotech315-02
Micro-ForcepsRWDF11020-11Autoclaved/Sterile
Non-essential amino acidsCytivaSH3023801
PBS (10x)ThermoFisher SciAM9625
Penicillin Streptomycin Glutamine (100x)Gibco103780-16
Poly-L-ornithine hydrobromide SigmaP3655-100MG
Sodium pyruvate (100 mM)Gibco11360-070
Spring scissorsRWDS11008-42Autoclaved/Sterile
Surgical bladeFeather08-916-5DSterile
T-25 flasksFisher10-126-9
T-75 flasks Fisher13-680-65
Tissue forcepsCodman30-4218Autoclaved/Sterile
Tissue scissorsRWDS12052-10Autoclaved/Sterile
Trypan Blue Thermofisher Sci 15250-061
Trypsin (2.5%)ThermoFisher Sci15090046
Widefield Immunofluorescence MicroscopeZeiss

References

  1. Yin, J., Valin, K. L., Dixon, M. L., Leavenworth, J. W. The role of microglia and macrophages in CNS homeostasis, autoimmunity, and cancer. J Immunol Res. 2017, 1-12 (2017).
  2. Colonna, M., Butovsky, O.

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MicrogliaCortical NeuronsCNSCo culturingNeuronal HealthNeurodegenerative DiseasesMultiple SclerosisIn Vitro ProtocolPrimary MicrogliaMixed Glia CultureBrain HomogenatesEmbryonic DaysImmunofluorescence MicroscopyRNA AssaysProtein Assays

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