Glia in amyotrophic lateral sclerosis and spinal cord injury: common therapeutic targets

被引:16
作者
Ban, Jelena [1 ]
Samano, Cynthia [2 ]
Mladinic, Miranda [1 ]
Munitic, Ivana [3 ]
机构
[1] Univ Rijeka, Dept Biotechnol, Lab Mol Neurobiol, Rijeka, Croatia
[2] Univ Autonoma Metropolitana, Unidad Cuajimalpa, Lab Biol Celular, Dept Ciencias Nat, Mexico City, DF, Mexico
[3] Univ Rijeka, Dept Biotechnol, Lab Mol Immunol, Rijeka, Croatia
关键词
NEURAL STEM-CELLS; ACUTE ISCHEMIC-STROKE; NECROSIS-FACTOR-ALPHA; BLOOD-BRAIN-BARRIER; DNA-BINDING PROTEIN; PHASE-I TRIAL; NF-KAPPA-B; MOUSE MODEL; FOCAL TRANSPLANTATION; DISEASE PROGRESSION;
D O I
10.3325/cmj.2019.60.109
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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. Neuroin flammation 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.
引用
收藏
页码:109 / 120
页数:12
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