Department of Microbiology-Immunology, Northwestern University Feinberg Medical School, 303 East Chicago Avenue, Chicago, IL, 60611, USA.
KM Application Center, Korea Institute of Oriental Medicine, Daegu, Republic of Korea.
J Neuroinflammation. 2020 Oct 17;17(1):307. doi: 10.1186/s12974-020-01986-z.
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.
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.
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.
实验性自身免疫性脑脊髓炎(EAE)和病毒性脱髓鞘疾病是两种用于研究人类多发性硬化症的主要实验模型系统。尽管先前在 EAE 和病毒性脱髓鞘疾病小鼠的中枢神经系统中观察到内皮素-1 水平升高,但内皮素-1 在这些脱髓鞘疾病发展中的潜在作用尚不清楚。
在这项研究中,使用这两种实验模型研究了内皮素-1 在脱髓鞘疾病发展和进展中的作用。内皮素-1 的给药显著促进了两种实验疾病的进展,同时伴有炎症性 T 细胞反应的升高。相比之下,特定的内皮素-1 抑制剂(BQ610 和 BQ788)的给药显著抑制了这些疾病的进展,同时伴有对各自抗原的 T 细胞反应减少。
这些结果强烈表明,内皮素-1 水平通过促进免疫反应在免疫介导的中枢神经系统脱髓鞘疾病的发病机制中发挥重要作用。