Ankeny D P, Popovich P G
Center for Brain and Spinal Cord Repair, Department of Molecular Virology, Immunology and Medical Genetics, The Ohio State University Medical Center, Biomedical Research Tower-Room 786, 460 West 12th Avenue, Columbus, OH 43210, USA.
Neuroscience. 2009 Feb 6;158(3):1112-21. doi: 10.1016/j.neuroscience.2008.07.001. Epub 2008 Jul 4.
Traumatic spinal cord injury (SCI) in mammals causes widespread glial activation and recruitment to the CNS of innate (e.g. neutrophils, monocytes) and adaptive (e.g. T and B lymphocytes) immune cells. To date, most studies have sought to understand or manipulate the post-traumatic functions of astrocytes, microglia, neutrophils or monocytes. Significantly less is known about the consequences of SCI-induced lymphocyte activation. Yet, emerging data suggest that T and B cells are activated by SCI and play significant roles in shaping post-traumatic inflammation and downstream cascades of neurodegeneration and repair. Here, we provide neurobiologists with a timely review of the mechanisms and implications of SCI-induced lymphocyte activation, including a discussion of different experimental strategies that have been designed to manipulate lymphocyte function for therapeutic gain.
哺乳动物的创伤性脊髓损伤(SCI)会导致广泛的胶质细胞活化,并吸引先天性免疫细胞(如中性粒细胞、单核细胞)和适应性免疫细胞(如T淋巴细胞和B淋巴细胞)进入中枢神经系统(CNS)。迄今为止,大多数研究都致力于了解或操纵星形胶质细胞、小胶质细胞、中性粒细胞或单核细胞在创伤后的功能。关于SCI诱导的淋巴细胞活化的后果,人们了解得要少得多。然而,新出现的数据表明,T细胞和B细胞会被SCI激活,并在塑造创伤后炎症以及神经退行性变和修复的下游级联反应中发挥重要作用。在此,我们为神经生物学家及时综述SCI诱导的淋巴细胞活化的机制及影响,包括对为了治疗获益而设计的不同实验策略的讨论,这些策略旨在操纵淋巴细胞功能。