Correlation Engine 2.0
Clear Search sequence regions


  • 3 utr (1)
  • ABCA1 (3)
  • abca1 protein (1)
  • ACAT1 (8)
  • acetyl coa (2)
  • atp (2)
  • cell (2)
  • cellular (1)
  • cholesterol (2)
  • cholesterol ester (3)
  • gene (2)
  • intracellular (1)
  • lipoprotein (1)
  • lipoproteins ldl (2)
  • low (1)
  • LPL (1)
  • macrophages (4)
  • mice (1)
  • micrornas (3)
  • MIRN467 (1)
  • oxldl (3)
  • regions (2)
  • regulates (3)
  • rna (1)
  • target gene (2)
  • Sizes of these terms reflect their relevance to your search.

    Previous studies have shown that miR-467b plays a central role in the progression of atherosclerosis via regulating LPL expression. However, the regulatory mechanism of miR-467b in regulateing the CE and FC formation is still unclear. Interestingly, computational analysis demonstrated that ACAT1 which converts intracellular FC into the storage form of CE, and ABCA1 which promotes cellular FC efflux may be target gene of miR-467b. Here, we examined whether miR-467b could target ACAT1 and ABCA1, thereby affecting the CE and FC formation in oxLDL-treatment RAW 264.7 cells. We found that miR-467b regulates the CE:FC ratio in oxLDL-treatment RAW 264.7 macrophages, and the luciferase activity of ACAT1 is regulated by the miR-467b, but the luciferase activity of ABCA1 has no effect. Furthermore, our data suggested that miR-467b highly regulates the endogenous levels of ACAT1 expression, thereby affecting the CE formation in oxLDL-treatment RAW 264.7 macrophages. Taken together, our findings demonstrate that ACAT1 is a target gene of miR-467b, and miR-467b regulated the CE and FC formation via directly target the ACAT1 3'UTR. Copyright © 2016. Published by Elsevier B.V.

    Citation

    Bo Wang, Ping-Ping He, Gao-Feng Zeng, Tao Zhang, Xin-Ping Ou Yang. miR-467b regulates the cholesterol ester formation via targeting ACAT1 gene in RAW 264.7 macrophages. Biochimie. 2017 Jan;132:38-44

    Expand section icon Mesh Tags

    Expand section icon Substances


    PMID: 27678191

    View Full Text