Department of Anthropology, School of Biomedical Sciences, Brain Health Research Institute, Kent State University, Kent, OH 44240, USA.
School of Biomedical Sciences, College of Arts and Sciences, Kent State University, Kent, OH 44240, USA.
Cells. 2021 May 8;10(5):1138. doi: 10.3390/cells10051138.
Microglia are the primary immune cells of the central nervous system that help nourish and support neurons, clear debris, and respond to foreign stimuli. Greatly impacted by their environment, microglia go through rapid changes in cell shape, gene expression, and functional behavior during states of infection, trauma, and neurodegeneration. Aging also has a profound effect on microglia, leading to chronic inflammation and an increase in the brain's susceptibility to neurodegenerative processes that occur in Alzheimer's disease. Despite the scientific community's growing knowledge in the field of neuroinflammation, the overall success rate of drug treatment for age-related and neurodegenerative diseases remains incredibly low. Potential reasons for the lack of translation from animal models to the clinic include the use of a single species model, an assumption of similarity in humans, and ignoring contradictory data or information from other species. To aid in the selection of validated and predictive animal models and to bridge the translational gap, this review evaluates similarities and differences among species in microglial activation and density, morphology and phenotype, cytokine expression, phagocytosis, and production of oxidative species in aging and Alzheimer's disease.
小胶质细胞是中枢神经系统的主要免疫细胞,有助于滋养和支持神经元、清除碎片,并对外部刺激做出反应。小胶质细胞受其环境影响很大,在感染、创伤和神经退行性变等状态下,其细胞形态、基因表达和功能行为会发生快速变化。衰老也对小胶质细胞产生深远影响,导致慢性炎症,并增加大脑对阿尔茨海默病等神经退行性过程的易感性。尽管科学界在神经炎症领域的知识不断增加,但针对与年龄相关和神经退行性疾病的药物治疗的总体成功率仍然非常低。从动物模型到临床应用缺乏转化的潜在原因包括使用单一物种模型、假设人类具有相似性以及忽略来自其他物种的矛盾数据或信息。为了帮助选择经过验证和可预测的动物模型并弥合转化差距,本综述评估了衰老和阿尔茨海默病中小胶质细胞激活和密度、形态和表型、细胞因子表达、吞噬作用以及氧化物质产生方面的物种间相似性和差异。