Maurya Shashank Kumar, Bhattacharya Neetu, Mishra Suman, Bhattacharya Amit, Banerjee Pratibha, Senapati Sabyasachi, Mishra Rajnikant
Department of Zoology, Ramjas College, University of Delhi, Delhi, India.
Department of Zoology, Dyal Singh College, University of Delhi, Delhi, India.
Front Pharmacol. 2021 Apr 13;12:654489. doi: 10.3389/fphar.2021.654489. eCollection 2021.
Microglia, a type of innate immune cell of the brain, regulates neurogenesis, immunological surveillance, redox imbalance, cognitive and behavioral changes under normal and pathological conditions like Alzheimer's, Parkinson's, Multiple sclerosis and traumatic brain injury. Microglia produces a wide variety of cytokines to maintain homeostasis. It also participates in synaptic pruning and regulation of neurons overproduction by phagocytosis of neural precursor cells. The phenotypes of microglia are regulated by the local microenvironment of neurons and astrocytes via interaction with both soluble and membrane-bound mediators. In case of neuron degeneration as observed in acute or chronic neurodegenerative diseases, microglia gets released from the inhibitory effect of neurons and astrocytes, showing activated phenotype either of its dual function. Microglia shows neuroprotective effect by secreting growths factors to heal neurons and clears cell debris through phagocytosis in case of a moderate stimulus. But the same microglia starts releasing pro-inflammatory cytokines like TNF-α, IFN-γ, reactive oxygen species (ROS), and nitric oxide (NO), increasing neuroinflammation and redox imbalance in the brain under chronic signals. Therefore, pharmacological targeting of microglia would be a promising strategy in the regulation of neuroinflammation, redox imbalance and oxidative stress in neurodegenerative diseases. Some studies present potentials of natural products like curcumin, resveratrol, cannabidiol, ginsenosides, flavonoids and sulforaphane to suppress activation of microglia. These natural products have also been proposed as effective therapeutics to regulate the progression of neurodegenerative diseases. The present review article intends to explain the molecular mechanisms and functions of microglia and molecular dynamics of microglia specific genes and proteins like Iba1 and Tmem119 in neurodegeneration. The possible interventions by curcumin, resveratrol, cannabidiol, ginsenosides, flavonoids and sulforaphane on microglia specific protein Iba1 suggest possibility of natural products mediated regulation of microglia phenotypes and its functions to control redox imbalance and neuroinflammation in management of Alzheimer's, Parkinson's and Multiple Sclerosis for microglia-mediated therapeutics.
小胶质细胞是大脑中的一种固有免疫细胞,在正常和病理条件下(如阿尔茨海默病、帕金森病、多发性硬化症和创伤性脑损伤)调节神经发生、免疫监视、氧化还原失衡、认知和行为变化。小胶质细胞产生多种细胞因子以维持体内平衡。它还通过吞噬神经前体细胞参与突触修剪和神经元过度产生的调节。小胶质细胞的表型通过与可溶性和膜结合介质的相互作用,由神经元和星形胶质细胞的局部微环境调节。在急性或慢性神经退行性疾病中观察到神经元退化的情况下,小胶质细胞从神经元和星形胶质细胞的抑制作用中释放出来,表现出其双重功能的激活表型。在适度刺激的情况下,小胶质细胞通过分泌生长因子来修复神经元并通过吞噬作用清除细胞碎片,从而发挥神经保护作用。但在慢性信号作用下,同样的小胶质细胞开始释放促炎细胞因子,如肿瘤坏死因子-α、干扰素-γ、活性氧(ROS)和一氧化氮(NO),增加大脑中的神经炎症和氧化还原失衡。因此,对小胶质细胞进行药物靶向治疗可能是调节神经退行性疾病中神经炎症、氧化还原失衡和氧化应激的一种有前景的策略。一些研究表明,姜黄素、白藜芦醇、大麻二酚、人参皂苷、类黄酮和萝卜硫素等天然产物具有抑制小胶质细胞激活的潜力。这些天然产物也被提议作为调节神经退行性疾病进展的有效疗法。本综述文章旨在解释小胶质细胞的分子机制和功能,以及小胶质细胞特异性基因和蛋白质(如Iba1和Tmem119)在神经退行性变中的分子动力学。姜黄素、白藜芦醇、大麻二酚、人参皂苷、类黄酮和萝卜硫素对小胶质细胞特异性蛋白Iba1的可能干预表明,天然产物有可能介导小胶质细胞表型及其功能的调节,以控制阿尔茨海默病、帕金森病和多发性硬化症治疗中由小胶质细胞介导的氧化还原失衡和神经炎症。