Pekny Milos, Wilhelmsson Ulrika, Pekna Marcela
Center for Brain Repair and Rehabilitation, Department of Clinical Neuroscience and Rehabilitation, Institute of Neuroscience and Physiology, Sahlgrenska Academy at the University of Gothenburg, Gothenburg SE-405 30, Sweden; Florey Institute of Neuroscience and Mental Health, Parkville, Victoria, Australia.
Center for Brain Repair and Rehabilitation, Department of Clinical Neuroscience and Rehabilitation, Institute of Neuroscience and Physiology, Sahlgrenska Academy at the University of Gothenburg, Gothenburg SE-405 30, Sweden.
Neurosci Lett. 2014 Apr 17;565:30-8. doi: 10.1016/j.neulet.2013.12.071. Epub 2014 Jan 7.
Astrocyte activation and reactive gliosis accompany most of the pathologies in the brain, spinal cord, and retina. Reactive gliosis has been described as constitutive, graded, multi-stage, and evolutionary conserved defensive astroglial reaction [Verkhratsky and Butt (2013) In: Glial Physiology and Pathophysiology]. A well- known feature of astrocyte activation and reactive gliosis are the increased production of intermediate filament proteins (also known as nanofilament proteins) and remodeling of the intermediate filament system of astrocytes. Activation of astrocytes is associated with changes in the expression of many genes and characteristic morphological hallmarks, and has important functional consequences in situations such as stroke, trauma, epilepsy, Alzheimer's disease (AD), and other neurodegenerative diseases. The impact of astrocyte activation and reactive gliosis on the pathogenesis of different neurological disorders is not yet fully understood but the available experimental evidence points to many beneficial aspects of astrocyte activation and reactive gliosis that range from isolation and sequestration of the affected region of the central nervous system (CNS) from the neighboring tissue that limits the lesion size to active neuroprotection and regulation of the CNS homeostasis in times of acute ischemic, osmotic, or other kinds of stress. The available experimental data from selected CNS pathologies suggest that if not resolved in time, reactive gliosis can exert inhibitory effects on several aspects of neuroplasticity and CNS regeneration and thus might become a target for future therapeutic interventions.
星形胶质细胞激活和反应性胶质增生伴随脑、脊髓和视网膜中的大多数病理情况。反应性胶质增生被描述为一种组成性、分级、多阶段且在进化上保守的防御性星形胶质细胞反应[韦赫拉茨基和巴特(2013年),载于《胶质细胞生理学与病理生理学》]。星形胶质细胞激活和反应性胶质增生的一个众所周知的特征是中间丝蛋白(也称为纳米丝蛋白)产生增加以及星形胶质细胞中间丝系统的重塑。星形胶质细胞的激活与许多基因表达的变化和特征性形态学标志相关,并在中风、创伤、癫痫、阿尔茨海默病(AD)和其他神经退行性疾病等情况下具有重要的功能后果。星形胶质细胞激活和反应性胶质增生对不同神经疾病发病机制的影响尚未完全了解,但现有实验证据表明星形胶质细胞激活和反应性胶质增生有许多有益方面,从将中枢神经系统(CNS)的受影响区域与邻近组织隔离和隔离以限制病变大小到在急性缺血、渗透压或其他类型应激时积极的神经保护和调节CNS内环境稳定。来自选定CNS病理的现有实验数据表明,如果不及时解决,反应性胶质增生可能对神经可塑性和CNS再生的多个方面产生抑制作用,因此可能成为未来治疗干预的靶点。