MicroRNA-181a-5p Curbs Osteogenic Differentiation and Bone Formation Partially Through Impairing Runx1-Dependent Inhibition of AIF-1 Transcription

被引:6
|
作者
Liu, Jingwei [1 ]
Chang, Xueying [2 ]
Dong, Daming [1 ,3 ]
机构
[1] Harbin Med Univ, Dept Orthoped, Affiliated Hosp 1, Harbin, Peoples R China
[2] Harbin Med Univ, Dept Nephrol, Affiliated Hosp 1, Harbin, Peoples R China
[3] Harbin Med Univ, Dept Orthoped, Affiliated Hosp 1, 23 Youzheng Rd, Harbin 150001, Heilongjiang, Peoples R China
关键词
MicroRNAs; Transcription factors; Ovariectomy; Osteoporosis; Osteogenesis; INFLAMMATORY FACTOR-I; OSTEOBLAST DIFFERENTIATION; CELLS; OSTEOPOROSIS; PATHOGENESIS; MICRORNAS;
D O I
10.3803/EnM.2022.1516
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Evidence has revealed the involvement of microRNAs (miRNAs) in modulating osteogenic differentiation, implying the promise of miRNA-based therapies for treating osteoporosis. This study investigated whether miR-181a-5p influences osteogen-ic differentiation and bone formation and aimed to establish the mechanisms in depth. Methods: Clinical serum samples were obtained from osteoporosis patients, and MC3T3-E1 cells were treated with osteogenic duction medium (OIM) to induce osteogenic differentiation. miR-181a-5p-, Runt-related transcription factor 1 (Runx1)-, and/or lograft inflammatory factor-1 (AIF-1)-associated oligonucleotides or vectors were transfected into MC3T3-E1 cells to explore their function in relation to the number of calcified nodules, alkaline phosphatase (ALP) staining and activity, expression levels of osteo-genesis-related proteins, and apoptosis. Luciferase activity, RNA immunoprecipitation, and chromatin immunoprecipitation assays were employed to validate the binding relationship between miR-181a-5p and Runx1, and the transcriptional regulatory relationship between Runx1 and AIF-1. Ovariectomy (OVX)-induced mice were injected with a miR-181a-5p antagonist for in vivo verification. Results: miR-181a-5p was highly expressed in the serum of osteoporosis patients. OIM treatment decreased miR-181a-5p and AIF-1 expression, but promoted Runx1 expression in MC3T-E1 cells. Meanwhile, upregulated miR-181a-5p suppressed OIM-induced increases in calcified nodules, ALP content, and osteogenesis-related protein expression. Mechanically, miR-181a-5p targeted Runx1, which acted as a transcription factor to negatively modulate AIF-1 expression. Downregulated Runx1 suppressed the miR-181a-5p inhibitor-mediated promotion of osteogenic differentiation, and downregulated AIF-1 reversed the miR-181a-5p mimic duced inhibition of osteogenic differentiation. Tail vein injection of a miR-181a-5p antagonist induced bone formation in OVX-in-duced osteoporotic mice. Conclusion: In conclusion, miR-181a-5p affects osteogenic differentiation and bone formation partially via the modulation of Runx1/AIF-1 axis.
引用
收藏
页码:156 / 173
页数:18
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