Ma Zhanjun, Dang Hong Anh, Yang Jingjing, Rodella Giulia, Mwema Ariane, De Lombaerde Emily, Chen Yong, De Geest Bruno G, van Pesch Vincent, Muccioli Giulio G, des Rieux Anne
Louvain Drug Research Institute, Advanced Drug Delivery and Biomaterials, Université Catholique de Louvain, UCLouvain, 1200, Brussels, Belgium; Louvain Drug Research Institute, Bioanalysis and Pharmacology of Bioactive Lipids, Université Catholique de Louvain, UCLouvain, 1200, Brussels, Belgium.
Institute of Neurosciences, Neurochemistry Group, Université Catholique de Louvain, UCLouvain, 1200, Brussels, Belgium.
Biomaterials. 2026 Feb;325:123589. doi: 10.1016/j.biomaterials.2025.123589. Epub 2025 Jul 29.
MicroRNAs (miRNAs) regulate many physiological and pathological processes implicated in numerous diseases, including neuroinflammatory disorders. Chronic neuroinflammation is a key feature of neurodegenerative diseases, yet effective medications remain unavailable. Delivery of exogenous miRNAs, such as miRNA-124 (miR-124), shows promise as a therapeutic approach as it promotes microglial polarization towards an anti-inflammatory phenotype. However, the options for robust drug delivery systems to enhance miRNA mimic stability and ability to penetrate the central nervous system (CNS) are limited. Here, for the first time, we propose an LNP formulation optimized for miR-124 delivery to the CNS. We compared several ionizable lipids and selected the one that provided the highest efficiency (both regarding cell uptake, transfection efficiency and inflammation modulation) and the lowest microglia activation (S-Ac7-DOG). In cultured BV2 and primary mixed glial cells, miR-124-LNP treatment downregulated the expression of pro-inflammatory and upregulated anti-inflammatory genes. Furthermore, local delivery into the prefrontal cortex as well as intravenous injection of miR-124-LNP in lipopolysaccharides (LPS)-treated mice effectively reduced inflammation, as evidenced by the lower expression of pro-inflammatory and higher levels of anti-inflammatory cytokines. Thus, we provide a rational screening of clinically relevant LNP ionizable lipids for miRNA delivery, the demonstration of the therapeutic efficacy of miR-124-S-Ac7-DOG LNP in an LPS-induced neuroinflammation model, and finally, a non-viral, clinically translatable delivery system for miRNA therapy in the CNS. Overall, this study highlights LNP as an effective miRNA delivery vehicle for CNS applications and as a versatile platform for exploring gene therapies targeting neuroinflammation.
