» Articles » PMID: 38851724

Characterization of Spinal Cord Tissue-derived Extracellular Vesicles in Neuroinflammation

Abstract

Extracellular vesicles (EVs) are released by all cells, can cross the blood-brain barrier, and have been shown to play an important role in cellular communication, substance shuttling, and immune modulation. In recent years EVs have shifted into focus in multiple sclerosis (MS) research as potential plasma biomarkers and therapeutic vehicles. Yet little is known about the disease-associated changes in EVs in the central nervous system (CNS). To address this gap, we characterized the physical and proteomic changes of mouse spinal cord-derived EVs before and at 16 and 25 days after the induction of experimental autoimmune encephalomyelitis (EAE), a neuroinflammatory model of MS. Using various bioinformatic tools, we found changes in inflammatory, glial, and synaptic proteins and pathways, as well as a shift in the predicted contribution of immune and glial cell types over time. These results show that EVs provide snapshots of crucial disease processes such as CNS-compartmentalized inflammation, re/de-myelination, and synaptic pathology, and might also mediate these processes. Additionally, inflammatory plasma EV biomarkers previously identified in people with MS were also altered in EAE spinal cord EVs, suggesting commonalities of EV-related pathological processes during EAE and MS and overlap of EV proteomic changes between CNS and circulating EVs.

References
1.
Bakhti M, Winter C, Simons M . Inhibition of myelin membrane sheath formation by oligodendrocyte-derived exosome-like vesicles. J Biol Chem. 2010; 286(1):787-96. PMC: 3013037. DOI: 10.1074/jbc.M110.190009. View

2.
Bhargava P, Nogueras-Ortiz C, Chawla S, Baek R, Jorgensen M, Kapogiannis D . Altered Levels of Toll-Like Receptors in Circulating Extracellular Vesicles in Multiple Sclerosis. Cells. 2019; 8(9). PMC: 6769450. DOI: 10.3390/cells8091058. View

3.
Welsh J, Goberdhan D, ODriscoll L, Buzas E, Blenkiron C, Bussolati B . Minimal information for studies of extracellular vesicles (MISEV2023): From basic to advanced approaches. J Extracell Vesicles. 2024; 13(2):e12404. PMC: 10850029. DOI: 10.1002/jev2.12404. View

4.
Kumar S, Frid M, Zhang H, Li M, Riddle S, Brown R . Complement-containing small extracellular vesicles from adventitial fibroblasts induce proinflammatory and metabolic reprogramming in macrophages. JCI Insight. 2021; 6(21). PMC: 8663554. DOI: 10.1172/jci.insight.148382. View

5.
Gharagozloo M, Smith M, Jin J, Garton T, Taylor M, Chao A . Complement component 3 from astrocytes mediates retinal ganglion cell loss during neuroinflammation. Acta Neuropathol. 2021; 142(5):899-915. PMC: 8713426. DOI: 10.1007/s00401-021-02366-4. View