中国组织工程研究2017，Vol.21Issue(21)：3287-3292,6.DOI:10.3969/j.issn.2095-4344.2017.21.002
miR-21/Sprouty1功能轴调控绝经后骨质疏松患者骨髓间充质干细胞的成骨能力
miR-21/Sprouty1 function axis regulates the osteogenic differentiation of bone marrow mesenchymal stem cells after postmenopausal osteoporosis
摘要
Abstract
BACKGROUND:Osteogenic differentiation is a complex process involving transcriptional and post-transcriptional regulation by multiple signaling pathways, and the specific mechanisms remain unclear. It is of great significance to study the role of critical miRNAs in the osteogenic differentiation of bone marrow mesenchymal stem cells (BMSCs) in the treatment of osteoporosis and bone defects. OBJECTIVE: To explore the regulatory ability of miR-21/Sprouty1 function axis in the osteogenic differentiation of BMSCs in patients with postmenopausal osteoporosis. METHODS:BMSCs were isolated from healthy people (H-hBMSCs) and patients with postmenopausal osteoporosis (PMOP-hBMSCs), and their osteogenic ability was compared. Expression of miR-21 and Spry1 at gene and protein levels was detected by real-time RT-PCR and western blot assay, respectively. miR-21 expression was upregulated via transfection in PMOP-hBMSCs, and the osteogenic ability and Spry1 expression of the cells were detected, while real-time RT-PCR and western blot were used to detect the expression of osteogenic marker genes, Runx2 and Osterix. RESULTS AND CONCLUSION:Compared with H-hBMSCs, PMOP-hBMSCs osteogenic ability was weakened significantly, miR-21 expression decreased, and Spry1 expression increased, indicating an inhibition to the miR-21-Spry1 function axis. Through the transfection of miR-21 and down-regulation of Spry1, the expression levels of Runx2 and Osterix were increased, and PMOP-hBMSCs osteogenic ability was partially restored.关键词
干细胞/骨髓干细胞/骨髓间充质干细胞/miR-21/绝经后骨质疏松/成骨分化/国家自然科学基金分类
医药卫生引用本文复制引用
杨楠,周威,王光,丁寅,金岩..miR-21/Sprouty1功能轴调控绝经后骨质疏松患者骨髓间充质干细胞的成骨能力[J].中国组织工程研究,2017,21(21):3287-3292,6.基金项目
国家重点基础研究发展计划(2011CB96700) （2011CB96700）
国家自然科学基金(81400854)the National Basic Research Program of China (973 Program), No. 2011CB96700 （81400854）
the National Natural Science Foundation of China, No. 81400854 （）
