» Articles » PMID: 24552578

What Are Exosomes and How Can They Be Used in Multiple Sclerosis Therapy?

Overview
Specialties Neurology
Pharmacology
Date 2014 Feb 21
PMID 24552578
Citations 31
Authors
Affiliations
Soon will be listed here.
Abstract

Current treatment options for multiple sclerosis are limited and consist of immunosuppressors or agents to prevent immune infiltration of the brain. These therapies have potentially harmful side effects and do little to promote myelin repair. Instead, we suggest using exosomes, naturally occurring small vesicles that exert influence through the delivery of mRNA, microRNA and protein. Dendritic cells can be cultured from bone marrow and stimulated to release exosomes. When administered to the brain, these exosomes significantly increase myelination and improve remyelination following injury by prompting preoligodendrocytes to differentiate into myelin producing cells. Additionally, they are non-toxic and can easily cross the blood-brain barrier and, thus, have great potential as a therapeutic.

Citing Articles

The role of mesenchymal stem cells in attenuating inflammatory bowel disease through ubiquitination.

Liao H, Mao X, Wang L, Wang N, Ocansey D, Wang B Front Immunol. 2024; 15:1423069.

PMID: 39185411 PMC: 11341407. DOI: 10.3389/fimmu.2024.1423069.


Exosome Content-Mediated Signaling Pathways in Multiple Sclerosis.

Mohammadinasr M, Montazersaheb S, Ayromlou H, Hosseini V, Molavi O, Hejazi M Mol Neurobiol. 2024; 61(8):5404-5417.

PMID: 38191693 DOI: 10.1007/s12035-023-03862-2.


Biogenesis, Composition and Potential Therapeutic Applications of Mesenchymal Stem Cells Derived Exosomes in Various Diseases.

Yuan Y, Wang J, Zhang Y, Li L, Reza A, Gurunathan S Int J Nanomedicine. 2023; 18:3177-3210.

PMID: 37337578 PMC: 10276992. DOI: 10.2147/IJN.S407029.


Insights into Exosome Transport through the Blood-Brain Barrier and the Potential Therapeutical Applications in Brain Diseases.

Abdelsalam M, Ahmed M, Osaid Z, Hamoudi R, Harati R Pharmaceuticals (Basel). 2023; 16(4).

PMID: 37111328 PMC: 10144189. DOI: 10.3390/ph16040571.


Multiplex Analysis of Cerebrospinal Fluid and Serum Exosomes MicroRNAs of Untreated Relapsing Remitting Multiple Sclerosis (RRMS) and Proposing Noninvasive Diagnostic Biomarkers.

Mohammadinasr M, Montazersaheb S, Molavi O, Kahroba H, Talebi M, Ayromlou H Neuromolecular Med. 2023; 25(3):402-414.

PMID: 37020076 DOI: 10.1007/s12017-023-08744-3.


References
1.
Zhao X, He X, Han X, Yu Y, Ye F, Chen Y . MicroRNA-mediated control of oligodendrocyte differentiation. Neuron. 2010; 65(5):612-26. PMC: 2855245. DOI: 10.1016/j.neuron.2010.02.018. View

2.
Fields R . White matter in learning, cognition and psychiatric disorders. Trends Neurosci. 2008; 31(7):361-70. PMC: 2486416. DOI: 10.1016/j.tins.2008.04.001. View

3.
Kuhlmann T, Miron V, Cui Q, Cuo Q, Wegner C, Antel J . Differentiation block of oligodendroglial progenitor cells as a cause for remyelination failure in chronic multiple sclerosis. Brain. 2008; 131(Pt 7):1749-58. DOI: 10.1093/brain/awn096. View

4.
Hartman Z, Wei J, Glass O, Guo H, Lei G, Yang X . Increasing vaccine potency through exosome antigen targeting. Vaccine. 2011; 29(50):9361-7. PMC: 3350974. DOI: 10.1016/j.vaccine.2011.09.133. View

5.
Mattson M, Duan W, Lee J, Guo Z . Suppression of brain aging and neurodegenerative disorders by dietary restriction and environmental enrichment: molecular mechanisms. Mech Ageing Dev. 2001; 122(7):757-78. DOI: 10.1016/s0047-6374(01)00226-3. View