4.7 Article

Omega-3 fatty acids impair miR-1-3p-dependent Notch3 down-regulation and alleviate sepsis-induced intestinal injury

期刊

MOLECULAR MEDICINE
卷 28, 期 1, 页码 -

出版社

SPRINGER
DOI: 10.1186/s10020-021-00425-w

关键词

Omega-3 fatty acids; microRNA-1-3p; Notch3; Smad; Sepsis; Intestinal injury; Inflammation; Stress oxidative

资金

  1. Guangdong Natural Science Foundation Project [2021A1515012119]
  2. Shenzhen's Sanming Project
  3. Shenzhen Key Laboratory of Prevention and Treatment of Severe Infections [ZDSYS20200811142804014]
  4. Shenzhen Key Medical Discipline Construction Fund [SZXK045]

向作者/读者索取更多资源

The study demonstrated that omega-3 fatty acids can protect against intestinal injury caused by sepsis by down-regulating miR-1-3p, resulting in reduced inflammation and oxidative stress levels. Additionally, miR-1-3p was found to down-regulate Notch3 to inactivate the Smad pathway, exacerbating intestinal inflammation and oxidative stress.
Background Sepsis is a troublesome syndrome that can cause intestinal injury and even high mortality rates. Omega-3 fatty acids (FAs) are known to protect against intestinal damage. Accordingly, the current study set out to explore if omega-3 FAs could affect sepsis-induced intestinal injury with the involvement of the microRNA (miR)-1-3p/Notch3-Smad axis. Methods First, cecal ligation and perforation (CLP) was performed to establish septic mouse models in C57BL/6J mice, and mouse intestinal epithelial MODE-K cells were induced by lipopolysaccharide (LPS) to establish sepsis cell models. The CLP-induced septic mice or LPS-exposed cells were subjected to treatment with Omega-3 FAs and activin (Smad signaling activator), miR-1-3p inhibitor and over-expressed/short hairpin RNA (oe-/sh)-Notch3 to explore their roles in inflammation, intestinal oxidative stress and cell apoptosis. A dual-luciferase reporter gene assay was further performed to verify the regulatory relationship between miR-1-3p and Notch3. Results Omega-3 FAs inhibited CLP-induced intestinal injury and ameliorated LPS-induced intestinal epithelial cell injury by down-regulating miR-1-3p, as evidenced by decreased levels of tumor necrosis factor-alpha, interleukin-1 beta (IL-1 beta) and IL-6, in addition to diminished levels of reactive oxygen species, malondialdehyde levels and superoxide dismutase activity. Furthermore, miR-1-3p could down-regulate Notch3, which inactivated the Smad pathway. Conclusion Collectively, our findings indicated that omega-3 FAs elevate the expression of Notch3 by down-regulating miR-1-3p, and then blocking the Smad pathway to alleviate intestinal epithelial inflammation and oxidative stress injury caused by sepsis.

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