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MicroRNA-146a protects against LPS-induced organ damage by inhibiting Notch1 in macrophage
Xiaozhi Bai1, Julei Zhang1, Mengyuan Cao2
1Department of Burns and Cutaneous Surgery, Xijing Hospital, the Fourth Military Medical University, 127 Changle West Road, Xi'an, Shaanxi 710032, China.
Abstract:
MicroRNA-146a is a well-studied microRNA participating in immune and inflammatory diseases, but its role in sepsis has not been investigated. Here in our study, we found increased level of microRNA-146a in macrophage stimulated by lipopolysaccharide. In addition, the mRNA level of Notch1 was also increased. Up-regulation of microRNA-146a by miR-146a-mimic alleviated inflammatory responses of macrophage, for the levels of IL-1β, IL-6 and CCL-2 were decreased, and the activation of NF-κB signaling was inhibited. The histological examination showed that microRNA-146a protected against organ damage in mice with lipopolysaccharide injection, and the level of inflammatory factors, Cr, BUN, AST and ALT in serum were all decreased, reflecting the alleviated inflammation and recovered organ function. Then predicting databases were used and Notch1 was predicted as one of the potential targets of microRNA-146a. Knockout of Notch1 in macrophage showed reduced secretion of inflammatory factors and attenuated activation of NF-κB signaling in response to lipopolysaccharide. Specifically knockout of Notch1 in macrophage protected mice from LPS induced organ damage and dysfunction. Therefore, we prove that miR-146a acts as an inhibitor of inflammation by targeting Notch1 in macrophage, therefore protects mice from organ damage in sepsis.
Insights
MicroRNA-146a reduces inflammation in sepsis by targeting Notch1 in macrophages. This protects against organ damage and dysfunction in mice, offering a potential therapeutic target for sepsis treatment.
Area of Science:
- Immunology
- Molecular Biology
- Pathology
Background:
- MicroRNA-146a is implicated in immune and inflammatory diseases.
- Its specific role in sepsis remains largely unexplored.
Purpose of the Study:
- To investigate the role of microRNA-146a in sepsis.
- To elucidate the underlying molecular mechanisms involving Notch1 and NF-κB signaling.
Main Methods:
- Macrophages were stimulated with lipopolysaccharide (LPS).
- MicroRNA-146a levels and Notch1 mRNA were quantified.
- Overexpression and knockout models were used in macrophages and mice.
- Inflammatory markers and organ function were assessed.
Main Results:
- LPS stimulation increased microRNA-146a and Notch1 mRNA in macrophages.
- MicroRNA-146a mimic reduced inflammatory responses (IL-1β, IL-6, CCL-2) and NF-κB activation.
- MicroRNA-146a protected mice from LPS-induced organ damage and improved organ function markers.
- Notch1 was identified as a target of microRNA-146a; its knockout mimicked microRNA-146a's anti-inflammatory effects.
Conclusions:
- MicroRNA-146a acts as an inflammation inhibitor in sepsis by targeting Notch1 in macrophages.
- This pathway protects against sepsis-induced organ damage and dysfunction.
- MicroRNA-146a represents a potential therapeutic target for sepsis.
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