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Endothelin-1 contributes to the development of virus-induced demyelinating disease. | LitMetric

Endothelin-1 contributes to the development of virus-induced demyelinating disease.

J Neuroinflammation

Department of Microbiology-Immunology, Northwestern University Feinberg Medical School, 303 East Chicago Avenue, Chicago, IL, 60611, USA.

Published: October 2020

AI Article Synopsis

  • Endothelin-1 levels are elevated in the central nervous system (CNS) of mouse models for experimental autoimmune encephalitis (EAE) and viral demyelinating diseases, indicating a potential link to multiple sclerosis.
  • Administration of endothelin-1 worsens the progression of these demyelinating diseases by increasing inflammatory T cell responses, while specific inhibitors like BQ610 and BQ788 can curb disease progression and T cell activity.
  • The study concludes that endothelin-1 is crucial in the development of immune-mediated CNS demyelinating diseases by enhancing immune responses.

Article Abstract

Background: Experimental autoimmune encephalitis (EAE) and virally induced demyelinating disease are two major experimental model systems used to study human multiple sclerosis. Although endothelin-1 level elevation was previously observed in the CNS of mice with EAE and viral demyelinating disease, the potential role of endothelin-1 in the development of these demyelinating diseases is unknown.

Methods And Results: In this study, the involvement of endothelin-1 in the development and progression of demyelinating diseases was investigated using these two experimental models. Administration of endothelin-1 significantly promoted the progression of both experimental diseases accompanied with elevated inflammatory T cell responses. In contrast, administration of specific endothelin-1 inhibitors (BQ610 and BQ788) significantly inhibited progression of these diseases accompanied with reduced T cell responses to the respective antigens.

Conclusions: These results strongly suggest that the level of endothelin-1 plays an important role in the pathogenesis of immune-mediated CNS demyelinating diseases by promoting immune responses.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7568825PMC
http://dx.doi.org/10.1186/s12974-020-01986-zDOI Listing

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