| Literature DB >> 26663087 |
Priyanka Kushwaha1, Vikram Khedgikar2, Deepika Sharma3, Tony Yuen4, Jyoti Gautam2, Naseer Ahmad2, Anirudha Karvande2, Prabhat R Mishra5, Prabodh K Trivedi3, Li Sun4, Sanjay K Bhadada6, Mone Zaidi7, Ritu Trivedi8.
Abstract
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.Entities:
Keywords: animal model; bone; bone morphogenetic protein (BMP); cell differentiation; drug discovery; gene silencing; histone deacetylase 1 (HDAC1); microRNA (miRNA); osteoblast; osteoporosis
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Year: 2015 PMID: 26663087 PMCID: PMC4759174 DOI: 10.1074/jbc.M115.687152
Source DB: PubMed Journal: J Biol Chem ISSN: 0021-9258 Impact factor: 5.157