Role of Microglia TLRs in Neurodegeneration
- PMID: 30333729
- PMCID: PMC6176466
- DOI: 10.3389/fncel.2018.00329
Role of Microglia TLRs in Neurodegeneration
Abstract
Toll-like receptors (TLRs) are a group of receptors widely distributed in the organism. In the central nervous system, they are expressed in neurons, astrocytes and microglia. Although their involvement in immunity is notorious, different articles have demonstrated their roles in physiological and pathological conditions, including neurodegeneration. There is increasing evidence of an involvement of TLRs, especially TLR2, 4 and 9 in neurodegenerative diseases such as Alzheimer's disease (AD), Parkinson's disease (PD), and amyotrophic lateral sclerosis (ALS). In this sense, their expression in microglia might modulate the activity of these cells, which in turn, lead to protective or deleterious effects over neurons and other cells. Therefore, TLRs might mediate the link between inflammation and neurodegenerative diseases. However, further studies have to be performed to elucidate the role of the other TLRs in these diseases and to further prove and confirm the pathophysiological role of all TLRs in neurodegeneration. In this article, we revise and summarize the current knowledge regarding the role of TLRs in neurodegeneration with the focus on the possible functions of these receptors in microglia.
Keywords: Alzheimer’s disease; Parkinson’s disease; inflammatory mediators; microglia; neurodegenerative diseases; neuroinflammation; toll-like receptors (TLRs).
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References
-
- Balducci C., Frasca A., Zotti M., La Vitola P., Mhillaj E., Grigoli E., et al. . (2017). Toll-like receptor 4-dependent glial cell activation mediates the impairment in memory establishment induced by β-amyloid oligomers in an acute mouse model of Alzheimer’s disease. Brain Behav. Immun. 60, 188–197. 10.1016/j.bbi.2016.10.012 - DOI - PubMed
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