Alzheimer's disease (AD) is an irreversible neurodegenerative illness and the exact etiology of the disease remains unknown. It is characterized by long preclinical and prodromal phases with pathological features including an accumulation of amyloid-beta (Aβ) peptides into extracellular Aβ plaques in the brain parenchyma and the formation of intracellular neurofibrillary tangles (NFTs) within neurons as a result of abnormal phosphorylation of microtubule-associated tau proteins. In addition, prominent activation of innate immune cells is also observed and/or followed by marked neuroinflammation. While such neuroinflammatory responses may function in a neuroprotective manner by clearing neurotoxic factors, they can also be neurotoxic by contributing to neurodegeneration via elevated levels of proinflammatory mediators and oxidative stress, and altered levels of neurotransmitters, that underlie pathological symptoms including synaptic and cognitive impairment, neuronal death, reduced memory, and neocortex and hippocampus malfunctions. Glial cells, particularly activated microglia and reactive astrocytes, appear to play critical and interactive roles in such dichotomous responses. Accumulating evidences clearly point to their critical involvement in the prevention, initiation, and progression, of neurodegenerative diseases, including AD. Here, we review recent findings on the roles of astrocyte-microglial interactions in neurodegeneration in the context of AD and discuss newly developed in vitro and in vivo experimental models that will enable more detailed analysis of glial interplay. An increased understanding of the roles of glia and the development of new exploratory tools are likely to be crucial for the development of new interventions for early stage AD prevention and cures.
Bibliographical noteFunding Information:
This research was supported by Pioneering Funding Award funded by Cure Alzheimer’s Fund (CAF, HaC), the Brain Research Program through the National Research Foundation of Korea(NRF) funded by the Ministry of Science and ICT (2018M3C7A1056682) (HeC and CL).
This research was supported by Pioneering Funding Award funded by Cure Alzheimer's Fund (CAF, HaC), the Brain Research Program through the National Research Foundation of Korea(NRF) funded by the Ministry of Science and ICT (2018M3C7A1056682) (HeC and CL).
© 2018 Chun, Marriott, Lee and Cho.
All Science Journal Classification (ASJC) codes
- Clinical Neurology