Rusty Microglia: Trainers of Innate Immunity in Alzheimer's Disease

Frontiers in Neurology

卷:9

Roberto Gradini¹  Amy I. Price²  Michael Cummings³  Adonis Sfera³  Eddie Diaz³  Carolina Osorio⁴ 

[1] Department of Pathology, La Sapienza University of Rome, Rome, Italy;

[2] Evidence Based Medicine, University of Oxford, Oxford, United Kingdom;

[3] Patton State Hospital, San Bernardino, CA, United States;

[4] Psychiatry, Loma Linda University, Loma Linda, CA, United States;

关键词: inflammasomes;    astrocytes;    microglia;    exosomes;    trained immunity;    tolerized immunity;   

DOI  :  10.3389/fneur.2018.01062

来源: DOAJ

【 摘 要 】

Alzheimer's disease, the most common form of dementia, is marked by progressive cognitive and functional impairment believed to reflect synaptic and neuronal loss. Recent preclinical data suggests that lipopolysaccharide (LPS)-activated microglia may contribute to the elimination of viable neurons and synapses by promoting a neurotoxic astrocytic phenotype, defined as A1. The innate immune cells, including microglia and astrocytes, can either facilitate or inhibit neuroinflammation in response to peripherally applied inflammatory stimuli, such as LPS. Depending on previous antigen encounters, these cells can assume activated (trained) or silenced (tolerized) phenotypes, augmenting or lowering inflammation. Iron, reactive oxygen species (ROS), and LPS, the cell wall component of gram-negative bacteria, are microglial activators, but only the latter can trigger immune tolerization. In Alzheimer's disease, tolerization may be impaired as elevated LPS levels, reported in this condition, fail to lower neuroinflammation. Iron is closely linked to immunity as it plays a key role in immune cells proliferation and maturation, but it is also indispensable to pathogens and malignancies which compete for its capture. Danger signals, including LPS, induce intracellular iron sequestration in innate immune cells to withhold it from pathogens. However, excess cytosolic iron increases the risk of inflammasomes' activation, microglial training and neuroinflammation. Moreover, it was suggested that free iron can awaken the dormant central nervous system (CNS) LPS-shedding microbes, engendering prolonged neuroinflammation that may override immune tolerization, triggering autoimmunity. In this review, we focus on iron-related innate immune pathology in Alzheimer's disease and discuss potential immunotherapeutic agents for microglial de-escalation along with possible delivery vehicles for these compounds.

【 授权许可】

Unknown