MiR-637 maintains the balance between adipocytes and osteoblasts by directly targeting Osterix

J Zhang, W Fu, M He, H Wang, W Wang… - Molecular biology of …, 2011 - Am Soc Cell Biol
J Zhang, W Fu, M He, H Wang, W Wang, S Yu, XW Bian, J Zhou, MCM Lin, G Lu, W Poon…
Molecular biology of the cell, 2011Am Soc Cell Biol
Bone development is dynamically regulated by homeostasis, in which a balance between
adipocytes and osteoblasts is maintained. Disruption of this differentiation balance leads to
various bone-related metabolic diseases, including osteoporosis. In the present study, a
primate-specific microRNA (miR-637) was found to be involved in the differentiation of
human mesenchymal stem cells (hMSCs). Our preliminary data indicated that miR-637
suppressed the growth of hMSCs and induced S-phase arrest. Expression of miR-637 was …
Bone development is dynamically regulated by homeostasis, in which a balance between adipocytes and osteoblasts is maintained. Disruption of this differentiation balance leads to various bone-related metabolic diseases, including osteoporosis. In the present study, a primate-specific microRNA (miR-637) was found to be involved in the differentiation of human mesenchymal stem cells (hMSCs). Our preliminary data indicated that miR-637 suppressed the growth of hMSCs and induced S-phase arrest. Expression of miR-637 was increased during adipocyte differentiation (AD), whereas it was decreased during osteoblast differentiation (OS), which suggests miR-637 could act as a mediator of adipoosteogenic differentiation. Osterix (Osx), a significant transcription factor of osteoblasts, was shown to be a direct target of miR-637, which significantly enhanced AD and suppressed OS in hMSCs through direct suppression of Osx expression. Furthermore, miR-637 also significantly enhanced de novo adipogenesis in nude mice. In conclusion, our data indicated that the expression of miR-637 was indispensable for maintaining the balance of adipocytes and osteoblasts. Disruption of miR-637 expression patterns leads to irreversible damage to the balance of differentiation in bone marrow.
Am Soc Cell Biol