4.7 Article

Effects of Adipose-Derived Biogenic Nanoparticle-Associated microRNA-451a on Toll-like Receptor 4-Induced Cytokines

Journal

PHARMACEUTICS
Volume 14, Issue 1, Pages -

Publisher

MDPI
DOI: 10.3390/pharmaceutics14010016

Keywords

exosome; extracellular vesicle; microRNA; microvesicle; Toll-like receptor 4

Funding

  1. Mayo Clinic Center for Regenerative Medicine in Florida
  2. Mayo Clinic Center for Biomedical Discovery
  3. Erik Compton Foundation
  4. National Institute of Allergy and Infectious Diseases, National Institutes of Health (NIH) [R21AI152318]
  5. American Heart Association [20TPA35490415]
  6. Programma Operativo Nazionale Ricerca e Innovazione, Italian Ministry of Education, University and Research, Italy [DOT13A8025]

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Extracellular vesicles (EVs) are nanoparticles released by cells that transfer biomolecules between cells. MicroRNAs (miRNAs/miRs) in EVs play a significant role in modulating signaling pathways in recipient cells. This study shows that miR-451a, abundant in EVs from adipose tissue, can suppress pro-inflammatory cytokines and enhance anti-inflammatory cytokines in the TLR4 pathway.
Extracellular vesicles (EVs) are cell-released nanoparticles that transfer biomolecular content between cells. Among EV-associated biomolecules, microRNAs (miRNAs/miRs) represent one of the most important modulators of signaling pathways in recipient cells. Previous studies have shown that EVs from adipose-derived mesenchymal stromal cells (MSCs) and adipose tissue modulate inflammatory pathways in macrophages. In this study, the effects of miRNAs that are abundant in adipose tissue EVs and other biogenic nanoparticles (BiNPs) were assessed in terms of altering Toll-like receptor 4 (TLR4)-induced cytokines. TLR-4 signaling in macrophages is often triggered by pathogen or damage-induced inflammation and is associated with several diseases. This study demonstrates that miR-451a, which is abundant in adipose tissue BiNPs, suppresses pro-inflammatory cytokines and increases anti-inflammatory cytokines associated with the TLR4 pathway. Therefore, miR-451a may be partially responsible for immunomodulatory effects of adipose tissue-derived BiNPs.

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