Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Concept Videos

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Regulatory B cells contribute to allergen-encapsulating nanoparticle immunotherapy efficacy for food allergy.

JCI insight·2026
Same author

Targeting fibrosis in the treatment of lower urinary tract dysfunction.

The Journal of pathology·2026
Same author

Myeloid Cell-Targeting PLGA Nanoparticles Ameliorate Acute Graft-Versus-Host Disease.

Cancers·2026
Same author

VEGFR Blockade Reduces <i>Mycobacterium tuberculosis</i>-Induced Lung Pathology in Immunocompromised Mice.

Cells·2026
Same author

Antigen-specific immunotherapy with a CD4<sup>+</sup> T cell neoepitope restrains CD8<sup>+</sup> T cell differentiation in murine pancreatic islet grafts.

Nature communications·2026
Same author

Cribriform Plate Microenvironment Assembles a Suppressive Myeloid Network during EAE-induced Neuroinflammation.

bioRxiv : the preprint server for biology·2026
Same journal

A Novel Laboratorial Approach to Evaluate Bacterial Microleakage of Endodontic Sealers.

Current protocols·2026
Same journal

TRIAGE Toolkit: Streamlined Discovery of Regulatory Genes and Elements.

Current protocols·2026
Same journal

High-throughput Profiling of Pseudouridines in Microbiome-derived Bacterial RNA.

Current protocols·2026
Same journal

Recombinant Protein Expression in Rhodococcus species.

Current protocols·2026
Same journal

Streamlined In Vitro Transcription for Generating Self-Amplifying RNA With Modified Nucleotides.

Current protocols·2026
Same journal

CODEC Library Preparation From Genomic DNA.

Current protocols·2026
See all related articles

Related Experiment Video

Updated: Oct 11, 2025

Author Spotlight: Creating a Versatile Experimental Autoimmune Encephalomyelitis Model Relevant for Both Male and Female Mice
05:44

Author Spotlight: Creating a Versatile Experimental Autoimmune Encephalomyelitis Model Relevant for Both Male and Female Mice

Published on: October 13, 2023

1.7K

Experimental Autoimmune Encephalomyelitis in the Mouse.

Collin Laaker1, Martin Hsu1, Zsuzsanna Fabry1

  • 1Department of Pathology and Lab Medicine, University of Wisconsin-Madison, Madison, Wisconsin.

Current Protocols
|December 6, 2021
PubMed
Summary
This summary is machine-generated.

This study provides detailed protocols for inducing experimental autoimmune encephalomyelitis (EAE) in mice using myelin proteins. It covers active and adoptive transfer methods for proteolipid protein (PLP), myelin basic protein (MBP), and myelin oligodendrocyte glycoprotein (MOG).

Keywords:
EAEMBPMOGPLPexperimental autoimmune encephalomyelitis

More Related Videos

Myelin Oligodendrocyte Glycoprotein MOG35-55 Induced Experimental Autoimmune Encephalomyelitis EAE in C57BL/6 Mice
08:03

Myelin Oligodendrocyte Glycoprotein MOG35-55 Induced Experimental Autoimmune Encephalomyelitis EAE in C57BL/6 Mice

Published on: April 15, 2014

82.7K
Induction of Experimental Autoimmune Encephalomyelitis in Mice and Evaluation of the Disease-dependent Distribution of Immune Cells in Various Tissues
08:47

Induction of Experimental Autoimmune Encephalomyelitis in Mice and Evaluation of the Disease-dependent Distribution of Immune Cells in Various Tissues

Published on: May 8, 2016

24.1K

Related Experiment Videos

Last Updated: Oct 11, 2025

Author Spotlight: Creating a Versatile Experimental Autoimmune Encephalomyelitis Model Relevant for Both Male and Female Mice
05:44

Author Spotlight: Creating a Versatile Experimental Autoimmune Encephalomyelitis Model Relevant for Both Male and Female Mice

Published on: October 13, 2023

1.7K
Myelin Oligodendrocyte Glycoprotein MOG35-55 Induced Experimental Autoimmune Encephalomyelitis EAE in C57BL/6 Mice
08:03

Myelin Oligodendrocyte Glycoprotein MOG35-55 Induced Experimental Autoimmune Encephalomyelitis EAE in C57BL/6 Mice

Published on: April 15, 2014

82.7K
Induction of Experimental Autoimmune Encephalomyelitis in Mice and Evaluation of the Disease-dependent Distribution of Immune Cells in Various Tissues
08:47

Induction of Experimental Autoimmune Encephalomyelitis in Mice and Evaluation of the Disease-dependent Distribution of Immune Cells in Various Tissues

Published on: May 8, 2016

24.1K

Area of Science:

  • Neuroimmunology
  • Autoimmune disease research
  • Animal models in neuroscience

Background:

  • Experimental autoimmune encephalomyelitis (EAE) is a widely used animal model for studying demyelinating diseases like multiple sclerosis.
  • Understanding the induction and transfer of EAE is crucial for investigating autoimmune responses against myelin.
  • Standardized protocols are essential for reproducible research in neuroimmunology.

Purpose of the Study:

  • To provide comprehensive materials and methods for active and adoptive transfer of EAE in specific mouse strains.
  • To detail the purification of key myelin proteins (PLP, MBP) and isolation of relevant lymphocytes.
  • To offer a resource for researchers working with EAE models, including potential modifications for other strains.

Main Methods:

  • Active induction of EAE in SJL mice using intact proteolipid protein (PLP) or myelin basic protein (MBP) proteins/peptides.
  • Adoptive transfer of EAE in SJL mice using PLP-, MBP-, or MOG-specific lymphocytes.
  • Active induction of EAE in C57BL/6 mice using myelin oligodendrocyte glycoprotein (MOG) peptide.
  • Purification protocols for PLP and MBP.
  • Isolation of central nervous system (CNS)-infiltrating lymphocytes from EAE mice.

Main Results:

  • Established protocols for successful active and adoptive induction of EAE in SJL and C57BL/6 mouse strains.
  • Detailed procedures for myelin protein purification and CNS lymphocyte isolation.
  • Demonstrated the utility of PLP, MBP, and MOG in EAE induction models.

Conclusions:

  • The provided protocols facilitate reproducible EAE induction and lymphocyte isolation for neuroimmunological studies.
  • This work serves as a valuable guide for researchers utilizing EAE models.
  • Adaptations may be needed for successful EAE induction in different mouse strains.