4.6 Article

MicroRNA 874-3p Exerts Skeletal Anabolic Effects Epigenetically during Weaning by Suppressing Hdac1 Expression

期刊

JOURNAL OF BIOLOGICAL CHEMISTRY
卷 291, 期 8, 页码 3959-3966

出版社

AMER SOC BIOCHEMISTRY MOLECULAR BIOLOGY INC
DOI: 10.1074/jbc.M115.687152

关键词

animal model; bone; bone morphogenetic protein (BMP); cell differentiation; drug discovery; gene silencing; histone deacetylase 1 (HDAC1); microRNA (miRNA); osteoblast; osteoporosis

资金

  1. CSIR [BSC0201]
  2. Department of Biotechnology [DBT-GAP0127]
  3. National Institutes of Health [DK80459, AG40132, AR06592, AR06066]

向作者/读者索取更多资源

Embryonic skeletogenesis and postnatal bone development require the transfer of calcium from the mother to the offspring during pregnancy and lactation. Therefore, bone resorption in the mother becomes elevated during these periods, resulting in significant maternal skeletal loss. There follows an anabolic phase around weaning during which there is a remarkable recovery of the maternal skeleton. However, the mechanism(s) of this anabolic response remain(s) largely unknown. We identified eight differentially expressed miRNAs by array profiling, of which miR-874-3p was highly expressed at weaning, a time when bone loss was noted to recover. We report that this weaning-associated miRNA is an anabolic target. Therefore, an agomir of miR-874-3p induced osteoblast differentiation and mineralization. These actions were mediated through the inhibition of Hdac1 expression and enhanced Runx2 transcriptional activation. When injected in vivo, the agomir significantly increased osteoblastogenesis and mineralization, reversed bone loss caused by ovariectomy, and increased bone strength. We speculate that elevated miR-874-3p expression during weaning enhances bone formation and that this miRNA may become a therapeutic target for conditions of bone loss.

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