Neurorestorative Roles of Microgliosis and Astrogliosis in Neuroinflammation and Neurodegeneration

B. Adetuyi, Pere-Ebi Toloyai, E. Ojugbeli, O. Oyebanjo, O. Adetuyi, C. Z. Uche, M. Olisah, O. Adumanya, C. J. Chikwendu, Johra Khan, Muhammad Akram, C. G. Awuchi, C. Egbuna
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引用次数: 1

Abstract

The pathophysiological processes involved in neurodegenerative diseases have not been clearly defined. Nevertheless, a significant aspect of the proof focuses directly on the function of several mechanisms of inflammation. The immune system is represented in the central nervous system by the microglial cell capable of detecting harmful or foreign pathogens, and thus initiates self-activation and neuro-inflammatory processes via phagocytosis and cytokines release, to maintain the cellular microenvironment. Then, microglial cells can spawn an emphasis on persistent inflammation that sometimes precedes or promote the neurodegenerative processes. Hence, the neuro-inflammatory micro-environment turns toxic and damaging to the neuronal cell, leading to degeneration and release of several factors which trigger an inflammatory reaction of the microglia, activating the neurodegenerative cycle. The biomechanical properties of the brain, neuronal regeneration, and plasticity can be modified by reactive gliosis. Defining the inception and development of reactive microgliosis and astrogliosis is vital for better clinical treatments design.
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小胶质细胞和星形胶质细胞在神经炎症和神经退行性变中的神经恢复作用
神经退行性疾病的病理生理过程尚未明确定义。然而,证据的一个重要方面直接集中在几种炎症机制的功能上。免疫系统在中枢神经系统中由能够检测有害或外来病原体的小胶质细胞代表,从而通过吞噬和细胞因子释放启动自我激活和神经炎症过程,以维持细胞微环境。然后,小胶质细胞可以产生持续性炎症,这种炎症有时先于或促进神经退行性过程。因此,神经炎症微环境对神经元细胞具有毒性和破坏性,导致退化并释放几种触发小胶质细胞炎症反应的因子,激活神经退行性循环。脑的生物力学特性、神经元再生和可塑性可以通过反应性胶质瘤来改变。明确反应性小胶质瘤和星形胶质瘤的起源和发展对更好的临床治疗设计至关重要。
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