| Literature DB >> 31825829 |
Alice Buonfiglioli1, Ibrahim E Efe2, Dilansu Guneykaya3, Andranik Ivanov4, Yimin Huang3, Elisabeth Orlowski3, Christina Krüger5, Rudolf A Deisz5, Darko Markovic6, Charlotte Flüh7, Andrew G Newman5, Ulf C Schneider8, Dieter Beule9, Susanne A Wolf10, Omar Dzaye11, David H Gutmann12, Marcus Semtner3, Helmut Kettenmann13, Seija Lehnardt14.
Abstract
Microglia express Toll-like receptors (TLRs) that sense pathogen- and host-derived factors, including single-stranded RNA. In the brain, let-7 microRNA (miRNA) family members are abundantly expressed, and some have recently been shown to serve as TLR7 ligands. We investigated whether let-7 miRNA family members differentially control microglia biology in health and disease. We found that a subset of let-7 miRNA family members function as signaling molecules to induce microglial release of inflammatory cytokines, modulate antigen presentation, and attenuate cell migration in a TLR7-dependent manner. The capability of the let-7 miRNAs to control microglial function is sequence specific, mapping to a let-7 UUGU motif. In human and murine glioblastoma/glioma, let-7 miRNAs are differentially expressed and reduce murine GL261 glioma growth in the same sequence-specific fashion through microglial TLR7. Taken together, these data establish let-7 miRNAs as key TLR7 signaling activators that serve to regulate the diverse functions of microglia in health and glioma.Entities:
Keywords: Toll-like receptor 7; glioblastoma; lethal-7; microRNA; microglia
Year: 2019 PMID: 31825829 DOI: 10.1016/j.celrep.2019.11.029
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423