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

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 a...

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Veröffentlicht in:The Journal of biological chemistry 2016-02, Vol.291 (8), p.3959-3966
Hauptverfasser: Kushwaha, Priyanka, Khedgikar, Vikram, Sharma, Deepika, Yuen, Tony, Gautam, Jyoti, Ahmad, Naseer, Karvande, Anirudha, Mishra, Prabhat R., Trivedi, Prabodh K., Sun, Li, Bhadada, Sanjay K., Zaidi, Mone, Trivedi, Ritu
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Sprache:eng
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Zusammenfassung: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.
ISSN:0021-9258
1083-351X
DOI:10.1074/jbc.M115.687152