miR-34a, a physical exercise regulator, involved in LncRNA CCAT2 signaling to regulate hepatic stellate cells proliferation

Abstract

In plasma, miR-34a could be one of potential biomarkers for frailty and is involved in the physiology processes which are benefit from exercise. One of its targets, Smad4 play important role in TGF-β1 pathway which is a dominant factor for balancing collagen production and degradation in hepatic stellate cells. TGF-β1/Smad4 regulated collagen deposition is a hallmark of hepatic fibrosis. Thus, miR-34a could be a link between exercise and hepatic disease. The potential regulation on miR-34a by LncRNAs in hepatic stellate cells (HSCs) is still reserved to be revealed. In current study, it was hypothesized that a miR-34a interactor, lncRNA CCAT2 may regulate TGF-β1 pathway in liver fibrotic remodeling. Dual luciferase activity showed CCAT2 and Smad4 are targets of miR-34a-5p. Sh-CCAT2 transfection prohibit HSCs proliferation and induce HSCs apoptosis, also inhibited ECM protein synthesis in HSCs. Decreased miR-34a-5p enhanced HSCs proliferation, blocked HSCs apoptosis and promoted ECM protein production. miR-34a-5p inhibitor undo protective regulation of sh-CCAT2 in liver fibrosis. Furthermore, clinical investigation showed that CCAT2 and Smad4 expression level were significantly induced, while miR-34a-5p was significantly decreased in HBV related liver fibrosis serum. In conclusion, activated HSCs via TGF-β1/Smad4 signaling pathway was successfully alleviated by CCAT2 inhibition through miR-34a-5p elevation.

Small-molecule natural products for reversing liver fibrosis based on modulation of HSCs activation: an update

“…MiR-21 activity changes reconnect the TGF-β signaling network and have an impact on HSCs phenotype in vitro [14] . MiR-34a promotes HSCs via the TGF-β pathway [15] . (2) Anti-fibrotic effects of miRNAs.…”