Name: Isolation of CNS Cell Types Using Magnetic Beads in Naive and EAE Mice
Uploaded: 2023-10-06T13:40:00
Duration: 1 min 32 s
Description: Watch this Scientific Journal Video about Isolation of CNS Cell Types Using Magnetic Beads in Naive and EAE Mice at JoVE.com

isolation of cns cell types using magnetic beads in naive and eae mice

Isolement simultané de tous les types de cellules résidentes du SNC chez les souris auto-immunes

Multiple sclerosis (MS) is a chronic inflammatory autoimmune disease of the central nervous system (CNS) characterized by demyelination, axonal damage, gliosis, and neurodegeneration. Despite numerous research approaches in this field, the pathophysiology of MS is still not fully understood1,2,3,4. The most common animal model for investigating MS is the myelin oligodendrocyte glycoprotein peptide 35-55 (MOG35-55)-induced experimental autoimmune encephalomyelitis (EAE) which shares many of its clinical and pathophysiological features5,6,7,8,9. It is based on the response of the immune system against CNS-specific antigens leading to inflammation, demyelination, and neuroaxonal degeneration. Experimental autoimmune encephalomyelitis (EAE) is a suitable model for the investigation of neuroinflammatory pathways and signaling cascades found in MS.
Current therapy options for MS are only partially effective and focus primarily on the initial inflammatory phase of the disease. However, the neurodegenerative component of MS seems to be the major challenge for long-term therapeutic approaches. Therefore, reproducible, and precise cell isolation protocols are required to investigate molecular and cellular mechanisms in autoimmune diseases in a comprehensive way. Even if some protocols for the isolation of one single cell type exist10,11,12,13,14,15, there is an unmet need for the simultaneous isolation of several CNS-resident cell populations at once. Previous protocols for the isolation of CNS-resident cells lack in preserving cellular functionality and purity, resulting in co-cultivation with neighboring cells16,17,18 or the unsuitability for complex analyses of intracellular networks ex vivo19,20,21,22.
The aim of this protocol was to establish a reproducible and comprehensive method for the simultaneous isolation of pure viable single-cell suspensions of all principal CNS-resident cell types applicable in adult healthy and EAE mice. The different cell types were isolated using magnetic-activated cell sorting (MACS)23. The cell separation can be accomplished either by positive selection, i.e., magnetic labeling of cell-type-specific surface markers, or by negative selection via biotinylation and depletion of all undesired cells. Flow cytometry was applied to ensure a purity of above 90% and a viability of at least 80% of the isolated single-cell suspensions.
In conclusion, the main goal was to establish a protocol for the simultaneous isolation of all main CNS-resident cell types as a versatile tool for the investigation of neuroinflammatory pathways offering a comprehensive and precise analysis of complex cellular networks and biochemical signaling cascades in healthy and EAE mice.

Pleins feux sur l’auteur : Étude des voies neuroinflammatoires par l’isolement simultané de tous les principaux types de cellules résidentes du SNC 

Isolement simultané de types de cellules résidentes du système nerveux central chez des souris adultes atteintes d’encéphalomyélite auto-immune

To investigate molecular and cellular mechanisms in autoimmune diseases such as multiple sclerosis, the generation of reproducible and sophisticated cell isolation protocols is an unmet need. Most of the current technologies to isolate and analyze CNS-resident cells show serious shortcomings, such as focusing on only one cell type or only postnatal mice. The current protocol for the simultaneous isolation of all main CNS-resident cell types from one CNS replicate offers the possibility to analyze complex neuronal networks and new inflammatory pathways, ex vivo from one single cell suspension, applicable to healthy mice and those with experimental autoimmune encephalomyelitis.Additionally, mice numbers are decreased Our protocol for the simultaneous isolation of all four major CNS-resident cell types in healthy and EAE mice could be used as a helpful tool for research groups studying new inflammatory pathways, allowing a much more accurate analysis of complex biomolecular mechanisms and cellular networks ex vivo. New scientific questions that could be answered with the help of our protocol are dynamic investigations in EAE during different stages of disease course, like neuroinflammation, neurodegeneration, and remission. Also, cell-cell interactions and biochemical pathways could be studied on an individual level.Likewise, functional assays could be performed with cultivated cells. We intend to focus on dynamic studies of the EAE course for multi-omic analysis from one individual CNS homogenate per EAE time point.

Watch this Scientific Journal Video about Isolation of CNS Cell Types Using Magnetic Beads in Naive and EAE Mice at JoVE.com

Isolation of CNS Cell Types Using Magnetic Beads in Naive and EAE Mice  

Isolement des types de cellules du SNC à l’aide de billes magnétiques chez les souris naïves et EAE

Pour commencer, divisez la suspension de cellules du SNC purifiée et non diluée de souris en deux fractions pour isoler davantage la microglie et les oligodendrocytes. Ajoutez ensuite à la suspension cellulaire respective une microbille marquée magnétiquement spécifique de l’antigène de surface pour différents types de cellules du SNC. Placez la colonne dans le champ magnétique, égalisez la colonne, puis ajoutez la suspension cellulaire résultante sur la colonne.Les cellules marquées magnétiquement seront conservées dans la colonne, et les cellules non étiquetées passeront à travers. Après avoir retiré la colonne du champ magnétique, rincez les cellules marquées magnétiquement de la colonne dans un tube en tant que fraction cellulaire sélectionnée positivement. Divisez le flux négatif des oligodendrocytes en deux fractions pour les isolements ultérieurs des neurones et des astrocytes.L’analyse par cytométrie en flux à l’aide de marqueurs spécifiques au type de cellule combinée à la discrimination des cellules vivantes ou mortes a permis d’obtenir des microglies, des oligodendrocytes, des astrocytes et des neurones. La caractérisation phénotypique des différentes populations cellulaires a montré que des suspensions unicellulaires d’une pureté et d’une viabilité d’environ 90 % ont été obtenues pour tous les principaux types de cellules résidentes du SNC.

Research

JoVE Journal

Neuroscience

Isolation of CNS Cell Types Using Magnetic Beads in Naive and EAE Mice

Simultaneous Isolation of Principal Central Nervous System-Resident Cell Types from Adult Autoimmune Encephalomyelitis Mice

Experimental autoimmune encephalomyelitis (EAE) is the most common murine model for multiple sclerosis (MS) and is frequently used to further elucidate ...

Recherche

Neurosciences

Preparation of CNS Tissue for Isolating Cells in EAE Mice 

Préparation de tissu SNC pour l’isolement de cellules chez des souris EAE 

Dissociation of CNS Tissue for Isolating Cells in EAE Mice 

Dissociation du tissu du SNC pour l’isolement des cellules chez les souris EAE 

Removal of Debris and Red Blood Cells from CNS Cell Suspension of EAE Mice

Élimination des débris et des globules rouges de la suspension des cellules du SNC chez les souris EAE