中国神经再生研究(英文版) ›› 2020, Vol. 15 ›› Issue (10): 1831-1837.doi: 10.4103/1673-5374.280307

• 综述:退行性病与再生 • 上一篇    下一篇

MicroRNAs作为实验性自身免疫性脑脊髓炎多发性硬化症模型的疾病进展生物标志物和治疗靶标

  

  • 出版日期:2020-10-15 发布日期:2020-08-06

MicroRNAs as disease progression biomarkers and therapeutic targets in experimental autoimmune encephalomyelitis model of multiple sclerosis

Bridget Martinez 1, 2 , Philip V. Peplow 3   

  1. 1 Physical Chemistry and Applied Spectroscopy, Chemistry Division, Los Alamos National Laboratory, Los Alamos, NM, USA
    2 Department of Medicine, St. Georges University School of Medicine, Grenada
    3 Department of Anatomy, University of Otago, Dunedin, New Zealand
  • Online:2020-10-15 Published:2020-08-06
  • Contact: Philip V. Peplow, PhD,phil.peplow@otago.ac.nz.

摘要: orcid: 0000-0001-5468-1989 (Philip V. Peplow)

Abstract: Multiple sclerosis is an autoimmune neurodegenerative disease of the central nervous system character- ized by pronounced inflammatory infiltrates entering the brain, spinal cord and optic nerve leading to demyelination. Focal demyelination is associated with relapsing-remitting multiple sclerosis, while pro- gressive forms of the disease show axonal degeneration and neuronal loss. The tests currently used in the clinical diagnosis and management of multiple sclerosis have limitations due to specificity and sensitivity. MicroRNAs (miRNAs) are dysregulated in many diseases and disorders including demyelinating and neu- roinflammatory diseases. A review of recent studies with the experimental autoimmune encephalomyelitis animal model (mostly female mice 6–12 weeks of age) has confirmed miRNAs as biomarkers of experimen- tal autoimmune encephalomyelitis disease and importantly at the pre-onset (asymptomatic) stage when assessed in blood plasma and urine exosomes, and spinal cord tissue. The expression of certain miRNAs was also dysregulated at the onset and peak of disease in blood plasma and urine exosomes, brain and spinal cord tissue, and at the post-peak (chronic) stage of experimental autoimmune encephalomyelitis dis- ease in spinal cord tissue. Therapies using miRNA mimics or inhibitors were found to delay the induction and alleviate the severity of experimental autoimmune encephalomyelitis disease. Interestingly, experimen- tal autoimmune encephalomyelitis disease severity was reduced by overexpression of miR-146a, miR-23b, miR-497, miR-26a, and miR-20b, or by suppression of miR-182, miR-181c, miR-223, miR-155, and miR- 873. Further studies are warranted on determining more fully miRNA profiles in blood plasma and urine exosomes of experimental autoimmune encephalomyelitis animals since they could serve as biomarkers of asymptomatic multiple sclerosis and disease course. Additionally, studies should be performed with male mice of a similar age, and with aged male and female mice.

Key words: animal model, blood plasma, blood serum, brain tissue, disease biomarkers, experimental autoimmune encephalomyelitis, microRNAs, multiple sclerosis, spinal cord, therapeutic targets, urine exosomes