Wang Han, Sun Zhongyang, Wang Yixuan, Hu Zebing, Zhou Hua, Zhang Lianchang, Hong Bo, Zhang Shu, Cao Xinsheng
The Key Laboratory of Aerospace Medicine, Ministry of Education, The Fourth Military Medical University, 710032, Xi'an, Shaanxi, China.
Department of orthopedics, No. 454 Hospital of PLA, 210002, Nanjing, Jiangsu, China.
Sci Rep. 2016 Mar 16;6:23170. doi: 10.1038/srep23170.
MicroRNAs (miRNAs) interfere with the translation of specific target mRNAs and are thought to thereby regulate many cellular processes. However, the role of miRNAs in osteoblast mechanotransduction remains to be defined. In this study, we investigated the ability of a miRNA to respond to different mechanical environments and regulate mechano-induced osteoblast differentiation. First, we demonstrated that miR-33-5p expressed by osteoblasts is sensitive to multiple mechanical environments, microgravity and fluid shear stress. We then confirmed the ability of miR-33-5p to promote osteoblast differentiation. Microgravity or fluid shear stress influences osteoblast differentiation partially via miR-33-5p. Through bioinformatics analysis and a luciferase assay, we subsequently confirmed that Hmga2 is a target gene of miR-33-5p that negatively regulates osteoblast differentiation. Moreover, miR-33-5p regulates osteoblast differentiation partially via Hmga2. In summary, our findings demonstrate that miR-33-5p is a novel mechano-sensitive miRNA that can promote osteoblast differentiation and participate in the regulation of differentiation induced by changes in the mechanical environment, suggesting this miRNA as a potential target for the treatment of pathological bone loss.
微小RNA(miRNA)可干扰特定靶标mRNA的翻译,被认为由此调控多种细胞过程。然而,miRNA在成骨细胞机械转导中的作用仍有待明确。在本研究中,我们探究了一种miRNA对不同机械环境作出反应并调控机械诱导的成骨细胞分化的能力。首先,我们证明了成骨细胞表达的miR-33-5p对多种机械环境、微重力和流体剪切应力敏感。然后,我们证实了miR-33-5p具有促进成骨细胞分化的能力。微重力或流体剪切应力部分通过miR-33-5p影响成骨细胞分化。通过生物信息学分析和荧光素酶测定,我们随后证实Hmga2是miR-33-5p的靶基因,其对成骨细胞分化起负调控作用。此外,miR-33-5p部分通过Hmga2调控成骨细胞分化。总之,我们的研究结果表明,miR-33-5p是一种新型的机械敏感miRNA,可促进成骨细胞分化并参与机械环境变化诱导的分化调控,提示该miRNA作为治疗病理性骨质流失的潜在靶点。