Abstract

Astrocytes actively regulate numerous cell types both within and outside of the central nervous system in health and disease. Indeed, astrocyte morphology, gene expression and function, alongside the content of astrocyte-derived extracellular vesicles (ADEVs), is significantly altered by ageing, inflammatory processes and in neurodegenerative diseases, such as Alzheimer’s disease, Parkinson’s disease and amyotrophic lateral sclerosis. Here, we review the relevant emerging literature focussed on perturbation in expression of microRNA (miRNA), small non-coding RNAs that potently regulate gene expression. Synthesis of this literature shows that ageing-related processes, neurodegenerative disease-associated mutations or peptides and cytokines induce dysregulated expression of miRNA in astrocytes and in some cases can lead to selective incorporation of miRNA into ADEVs. Analysis of the miRNA targets shows that the resulting downstream consequences of alterations to levels of miRNA include release of cytokines, chronic activation of the immune response, increased apoptosis, and compromised cellular functioning of both astrocytes and ADEV-ingesting cells. We conclude that perturbation of these functions likely exacerbates mechanisms leading to neuropathology and ultimately contributes to the cognitive or motor symptoms of neurodegenerative diseases. This field requires comprehensive miRNA expression profiling of both astrocytes and ADEVs to fully understand the effect of perturbed astrocytic miRNA expression in ageing and neurodegenerative disease.

Highlights

  • Astrocytes are highly ramified glial cells found throughout the central nervous system (CNS)

  • As complement factor H (CFH) acts as an inhibitor of the complement cascade, the miR-146a5p-mediated downregulation of CFH combined with IRAK2 upregulation following astrocytic exposure to Aβ is likely to result in sustained activation of the immune response, with the enhanced astrocytic production and secretion of NFκBregulated pro-inflammatory cytokines contributing to continued activation of both microglia and astrocytes (Li et al, 2011; Figure 1A)

  • Altered activity of key transcription factors (TFs) in astrocytes appears to result in aberrant transcription of miRNA which affects the health and function of surrounding cells, neurons

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Summary

Introduction

Astrocytes are highly ramified glial cells found throughout the central nervous system (CNS). HO-1-induced alterations to astrocytic miRNA expression may contribute to the increased risk of developing a neurodegenerative disease in older age.

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