IL-6-Mediated Upregulated miRNAs in Extracellular Vesicles Derived from Lund Human Mesencephalic (LUHMES) Cells: Effects on Astrocytes and Microglia

• Published in: Biomolecules (Basel, Switzerland) Vol. 13; no. 5; p. 718
• Main Authors: Nishi, Kento, Izumi, Hiroto, Tomonaga, Taisuke, Nagano, Chikage, Morimoto, Yasuo, Horie, Seichi
• Format: Journal Article
• Language: English
• Published: Switzerland MDPI AG 22-04-2023; MDPI
• Subjects: Adenosine triphosphate; Antibodies; astrocyte; Astrocytes; Astrocytes - metabolism; Cell culture; Depression, Mental; Exosomes; Extracellular vesicles; Extracellular Vesicles - genetics; Extracellular Vesicles - metabolism; Gene expression; Humans; IL-6; Interleukin 6; Interleukin-6 - genetics; Interleukin-6 - metabolism; Mental depression; Mental disorders; Microglia; Microglia - metabolism; MicroRNA; MicroRNAs; MicroRNAs - genetics; MicroRNAs - metabolism; miRNA; Nanofiltration; neural precursor cells; Neural Stem Cells - metabolism; Neurophysiology; Physiological aspects; Plasmids; Psychological aspects; Reagents; Regeneration; Stress (Psychology); Japan; United States > US; stress; extracellular vesicles; microRNA; depression; astrocyte; microglia; IL-6; neural precursor cells
• ISSN: 2218-273X; 2218-273X
• DOI: 10.3390/biom13050718

Psychological stress plays a major role in depression, and interleukin-6 (IL-6) is elevated during depression and psychological stress. MicroRNAs (miRNAs) in extracellular vesicles (EVs), including exosomes and microvesicles, suppress mRNA expression in other cells when endocytosed. In this study, we analyzed the effect of IL-6 on EVs secreted by neural precursor cells. Cells from the human immortalized neural precursor cell line LUHMES were treated with IL-6. EVs were collected using a nanofiltration method. We then analyzed the uptake of LUHMES-derived EVs by astrocytes (ACs) and microglia (MG). Microarray analysis of miRNAs was performed using EV-incorporated RNA and intracellular RNA from ACs and MG to search for increased numbers of miRNAs. We applied the miRNAs to ACs and MG, and examined the cells for suppressed mRNAs. IL-6 increased several miRNAs in the EVs. Three of these miRNAs were originally low in ACs and MG (hsa-miR-135a-3p, hsa-miR-6790-3p, and hsa-miR-11399). In ACs and MG, hsa-miR-6790-3p and hsa-miR-11399 suppressed four mRNAs involved in nerve regeneration (NREP, KCTD12, LLPH, and CTNND1). IL-6 altered the types of miRNAs in EVs derived from neural precursor cells, by which mRNAs involved in nerve regeneration were decreased in ACs and MG. These findings provide new insights into the involvement of IL-6 in stress and depression.