Muñoz-San Martín María, de la Guerra-Sasián Lucía, Gárate Gabriel, Madera Jorge, González-Suárez Andrea, Cavada-Bustamante Nadia C, González-Quintanilla Vicente, Dowling Jennifer K
Brain Inflammation Group Ireland (BIGie), School of Pharmacy and Biomolecular Sciences, Royal College of Surgeons in Ireland, 123 St. Stephen's Green, D02 YN77 Dublin, Ireland.
Instituto de Investigación Marqués de Valdecilla (IDIVAL), Hospital Universitario Marqués de Valdecilla & Universidad de Cantabria, Avda. Cardenal Herrera Oria s/n, 39011 Santander, Spain.
Int J Mol Sci. 2025 Sep 8;26(17):8740. doi: 10.3390/ijms26178740.
Beyond the potential role of microRNAs (miRNAs) as biomarkers, their participation in different biological and pathological processes observed in multiple sclerosis (MS) such as neuroinflammation, neurodegeneration and remyelination, makes them suitable candidates for therapeutic applications in neurorepair. Most studies addressing this reparative approach have been carried out using in vitro or in vivo model systems. However, functional differences between murine and human cells within the central nervous system (CNS) have been described, and certain mechanisms are distinctive in humans. The development of human models to investigate therapeutic interventions in neurological conditions including MS should be a priority to avoid failures. In this review, we provide a comprehensive summary of the advances in reparative therapeutic strategies for MS, including miRNAs and human models. We also discuss their benefits, the likely challenges they face and comment on possible mitigation strategies.
除了微小RNA(miRNA)作为生物标志物的潜在作用外,它们参与了在多发性硬化症(MS)中观察到的不同生物学和病理过程,如神经炎症、神经退行性变和髓鞘再生,这使得它们成为神经修复治疗应用的合适候选者。大多数针对这种修复方法的研究都是使用体外或体内模型系统进行的。然而,已经描述了中枢神经系统(CNS)内小鼠和人类细胞之间的功能差异,并且某些机制在人类中是独特的。开发用于研究包括MS在内的神经系统疾病治疗干预的人类模型应该是避免失败的优先事项。在这篇综述中,我们全面总结了MS修复治疗策略的进展,包括miRNA和人类模型。我们还讨论了它们的益处、可能面临的挑战,并对可能缓解策略进行了评论。