AUTHOR=Yin Chong , Tian Ye , Yu Yang , Yang Chaofei , Su Peihong , Zhao Yipu , Wang Xue , Zhang Kewen , Pei Jiawei , Li Dijie , Chen Zhihao , Zhang Yan , Miao Zhiping , Qian Airong 

TITLE=miR-129-5p Inhibits Bone Formation Through TCF4

JOURNAL=Frontiers in Cell and Developmental Biology

VOLUME=Volume 8 - 2020

YEAR=2020

URL=https://www.frontiersin.org/journals/cell-and-developmental-biology/articles/10.3389/fcell.2020.600641

DOI=10.3389/fcell.2020.600641

ISSN=2296-634X

ABSTRACT=Osteoporosis is a frequently-occurring bone disease in middle-aged and aged men and women. However, current therapies on this disease are still not ideal. miRNA is a class of endogenous non-protein-coding RNA with a length of 18-25 nucleotides. miRNA have been identified as important regulators for development, metabolism, carcinogenesis and bone formation. miR-129-5p has been reported as a regulator of cancer and neuroscience, while studies about its function on bone formation is still limited. In this study, we investigated the function and mechanism of miR-129-5p on osteoblast differentiation and bone formation.

We have assessed the expression of miRNAs in bone mesenchymal stem cells (BMSCs) from aging and menopause osteoporosis C57BL6 mice. The expression of miR-129-5p was altered in all osteoporosis models. Besides, the expression of miR-129-5p was negatively correlated with osteoblastic differentiation markers in the femur tissues of C57BL/6 mice of different ages. We further demonstrated that over-expression of miR-129-5p inhibited osteoblast differentiation in MC3T3-E1 cell line as well as bone formation of C57BL/6 mice. On the other hand, down-regulation of miR-129-5p enhanced osteoblast differentiation and bone formation. We also found that miR-129-5p inhibited wnt/β-catenin pathway in osteoblast. The target gene of miR-129-5p have been forecasted and proved as Tcf4. We further found that plasmid containing Tcf4 3’UTR sequence enhanced osteoblast differentiation as well as wnt/β-catenin pathway in MC3T3-E1 cells. To further investigate the rescue effect of miR-129-5p inhibitor, we manufactured bioengineered novel recombinant miR-129-5p inhibitor through E. coli system, and then tested its function. The results showed that the novel recombinant miR-129-5p inhibitor promoted osteoblast differentiation, and greatly ameliorated menopause osteoporosis in C57BL6 mice.

In conclusion, we have discovered miR-129-5p as an inhibitor of bone formation. miR-129-5p inhibited downstream transcription factors of wnt/β-catenin pathway through targeting Tcf4. Moreover, novel recombinant miR-129-5p inhibitor showed rescue effect on osteoporosis. This study has revealed a new mechanism of osteogenic differentiation and provided novel therapeutic strategies for treatment of skeletal disorders.