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.

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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