Temporal shifts in microRNAs signify the inflammatory state of primary murine microglial cells

Abstract

The primary function of microglia is to maintain brain homeostasis. However, in several neurodegenerative diseases, such as Alzheimers disease, the pathophysiological hallmarks that drive disease progression involve neurotoxicity and alterations in neuroinflammation. In this study, we exposed murine neonatal primary microglial cultures to external signals that mimic the in vivo stimuli caused by pathogens, injury, or toxic agents. In the presence of benzoyl ATP (bzATP) and lipopolysaccharide (LPS), we observed a coordinated increase in the expression of interleukins and chemokines. We focused on the dynamics of the differentially expressed microRNAs (miRNAs) that are statistically significant (DEMs) and tracked their post-activation dynamics. Monitoring miRNAs 3 and 8 hours (h) post-activation revealed robust changes in 33 and 57 DEMs, most of which were upregulated. The DEMs exhibiting the strongest temporal regulation included miR-155, miR-132, miR-3473e, miR-222, and miR-146b. Additionally, a strong downregulation of miR-3963 was attributed to the exposure to bzATP. Through their regulation of TNF and NF{kappa}B signaling pathways, the identified DEMs reflect the cellular response to inflammatory signals. We incubated the activated cells with ladostigil, a neuroprotective compound that has been shown to reduce oxidative stress, inflammation, and cognitive decline. While there was no significant effect 3 h post-activation, at 8 h, a few miRNAs implicated in inflammation suppression such as miR-27a, miR-27b, and miR-23b were upregulated in a ladostigil-dependent manner. We conclude that the miRNA expression profile provides a sensitive indicator of the regulatory mechanisms underlying inflammation-related responses in microglia. We propose that primary microglia subjected to controlled activation paradigms can serve as a robust model for inflammatory states in the brain to monitor the aging brain along the progression of neurodegenerative diseases.