Brain innate immune response via miRNA-TLR7 sensing in polymicrobial sepsis

• Published in: Brain, behavior, and immunity behavior, and immunity, 2022-02, Vol.100, p.10-24
• Main Authors: Zou, Lin, He, Junyun, Gu, Lili, Shahror, Rami A., Li, Yun, Cao, Tuoxin, Wang, Sheng, Zhu, Jing, Huang, Huang, Chen, Fengqian, Fan, Xiaoxuan, Wu, Junfang, Chao, Wei
• Format: Article
• Language: English
• Subjects: Animals; Behavior; Brain - metabolism; Cytokines; Cytokines - metabolism; Encephalopathy; Extracellular RNA; IL-6; Immunity, Innate; Innate immunity; Membrane Glycoproteins; Mice; Mice, Inbred C57BL; MicroRNA; MicroRNAs - genetics; MicroRNAs - metabolism; Neuroinflammation; Sepsis; TLR7; Toll-Like Receptor 7 - genetics; Toll-Like Receptor 7 - metabolism
• ISSN: 0889-1591; 1090-2139
• DOI: 10.1016/j.bbi.2021.11.007

•Sepsis triggers release of host cellular microRNAs into the circulation.•Exogenous miR-146a-5p induces brain inflammation via the TLR7.•Depletion of miR-146a reduced number of monocytes and neutrophils in the brain.•TLR7 deficiency reduced some aspects of inflammation in the brain following sepsis.•Ablation of TLR7 did not affect neurobehavioral recovery following sepsis. Sepsis-associated encephalopathy (SAE) occurs in sepsis survivors and is associated with breakdown of the blood–brain barrier (BBB), brain inflammation, and neurological dysfunction. We have previously identified a group of extracellular microRNAs (ex-miRNAs), such as miR-146a-5p, that were upregulated in the plasma of septic mice and human, and capable of inducing potent pro-inflammatory cytokines and complements. Here, we established a clinically relevant mouse model of SAE and investigated the role of extracellular miRNAs and their sensor Toll-like receptor 7 (TLR7) in brain inflammation and neurological dysfunction. We observed BBB disruption and a profound neuroinflammatory responses in the brain for up to 14 days post-sepsis; these included increased pro-inflammatory cytokines production, microglial expansion, and peripheral leukocyte accumulation in the CNS. In a battery of neurobehavioral tests, septic mice displayed impairment of motor coordination and neurological function. Sepsis significantly increased plasma RNA and miRNA levels for up to 7 days, such as miR-146a-5p. Exogenously added miR-146a-5p induces innate immune responses in both cultured microglia/astrocytes and the intact brain via a TLR7-dependent manner. Moreover, mice genetically deficient of miR-146a showed reduced accumulation of monocytes and neutrophils in the brain compared to WT after sepsis. Finally, ablation of TLR7 in the TLR7-/- mice preserved BBB integrity, reduced microglial expansion and leukocyte accumulation, and attenuated GSK3β signaling in the brain, but did not improve neurobehavioral recovery following sepsis. Taken together, these data establish an important role of extracellular miRNA and TLR7 sensing in sepsis-induced brain inflammation.