4.8 Article

let-7 MicroRNAs Regulate Microglial Function and Suppress Glioma Growth through Toll-Like Receptor 7

Journal

CELL REPORTS
Volume 29, Issue 11, Pages 3460-+

Publisher

CELL PRESS
DOI: 10.1016/j.celrep.2019.11.029

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Funding

  1. Deutsche Forschungsgemeinschaft [LE 2420/2-1, SFB-TRR167/B3]
  2. Alexander von Humboldt Award
  3. Berliner Krebsgesellschaft e.V.
  4. Monika Kutzner Foundation
  5. BIH-Charite Clinician Scientist Program
  6. Medical Neuroscience graduate program of Charite, Berlin
  7. NeuroCure [Exc 257]
  8. Berlin Institute of Health/Einstein Fellowship grant

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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.

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