Ban Jelena, Sámano Cynthia, Mladinic Miranda, Munitic Ivana
Ivana Munitic, Department of Biotechnology, University of Rijeka, R. Matejčić 2, 51000 Rijeka, Croatia,
Croat Med J. 2019 Apr 30;60(2):109-120. doi: 10.3325/cmj.2019.60.109.
The toolkit for repairing damaged neurons in amyotrophic lateral sclerosis (ALS) and spinal cord injury (SCI) is extremely limited. Here, we reviewed the in vitro and in vivo studies and clinical trials on nonneuronal cells in the neurodegenerative processes common to both these conditions. Special focus was directed to microglia and astrocytes, because their activation and proliferation, also known as neuroinflammation, is a key driver of neurodegeneration. Neuroinflammation is a multifaceted process that evolves during the disease course, and can be either beneficial or toxic to neurons. Given the fundamental regulatory functions of glia, pathogenic mechanisms in neuroinflammation represent promising therapeutic targets. We also discussed neuroprotective, immunosuppressive, and stem-cell based approaches applicable to both ALS and SCI.
用于修复肌萎缩侧索硬化症(ALS)和脊髓损伤(SCI)中受损神经元的工具极为有限。在此,我们回顾了关于这两种病症共有的神经退行性过程中非神经元细胞的体外和体内研究及临床试验。特别关注了小胶质细胞和星形胶质细胞,因为它们的激活和增殖,即神经炎症,是神经退行性变的关键驱动因素。神经炎症是一个多方面的过程,在疾病进程中演变,对神经元可能有益也可能有毒。鉴于胶质细胞的基本调节功能,神经炎症中的致病机制是很有前景的治疗靶点。我们还讨论了适用于ALS和SCI的神经保护、免疫抑制以及基于干细胞的方法。