运动通过激活长非编码 RNA H19/microRNA-149轴促进成骨分化

Xu-Chang Zhou, Dong-Xue Wang, Chun-Yu Zhang, Ya-Jing Yang, Ruo-Bing Zhao, Shengyao Liu, Guo-Xin Ni
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摘要

背景 在儿童和青少年时期进行有规律的体育锻炼有利于骨骼发育,因为体育锻炼能够通过促进骨骼形成来增加骨密度和峰值骨量。目的 研究运动对生长期小鼠骨形成的影响,并探究其潜在机制。方法 将 20 只生长期小鼠随机分为两组:Con组(对照组,n = 10)和Ex组(跑步机运动组,n = 10)。采用血红素-伊红染色法、免疫组化法和显微 CT 扫描法评估小鼠股骨的骨形成相关指标。生物信息学分析用于寻找长非编码 RNA H19(lncRNA H19)的潜在 miRNAs 靶点。利用 RT-qPCR 和 Western Blot 确认 lncRNA H19 潜在的 miRNA 靶基因以及 lncRNA H19 在促进成骨分化中的作用。结果 与 Con 组相比,骨形态发生蛋白 2 的表达也明显增加。micro-CT结果显示,8周中等强度跑步机运动能显著增加小鼠股骨的骨矿密度、骨体积分数和骨小梁数量,并减少骨小梁分离。抑制lncRNA H19可明显上调miR-149的表达,抑制成骨分化标志物的表达。此外,敲除lncRNA H19能明显下调自噬标记物的表达,这与免疫荧光法检测到的小鼠股骨中自噬相关蛋白变化的结果一致。结论 适当的跑步机运动能有效刺激骨形成,促进生长期小鼠骨密度和骨量的增加,从而提高小鼠的峰值骨量。lncRNA H19/miR-149轴在成骨分化中起着重要的调控作用。
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Exercise promotes osteogenic differentiation by activating the long non-coding RNA H19/microRNA-149 axis
BACKGROUND Regular physical activity during childhood and adolescence is beneficial to bone development, as evidenced by the ability to increase bone density and peak bone mass by promoting bone formation. AIM To investigate the effects of exercise on bone formation in growing mice and to investigate the underlying mechanisms. METHODS 20 growing mice were randomly divided into two groups: Con group (control group, n = 10) and Ex group (treadmill exercise group, n = 10). Hematoxylin-eosin staining, immunohistochemistry, and micro-CT scanning were used to assess the bone formation-related indexes of the mouse femur. Bioinformatics analysis was used to find potential miRNAs targets of long non-coding RNA H19 (lncRNA H19). RT-qPCR and Western Blot were used to confirm potential miRNA target genes of lncRNA H19 and the role of lncRNA H19 in promoting osteogenic differentiation. RESULTS Compared with the Con group, the expression of bone morphogenetic protein 2 was also significantly increased. The micro-CT results showed that 8 wk moderate-intensity treadmill exercise significantly increased bone mineral density, bone volume fraction, and the number of trabeculae, and decreased trabecular segregation in the femur of mice. Inhibition of lncRNA H19 significantly upregulated the expression of miR-149 and suppressed the expression of markers of osteogenic differentiation. In addition, knockdown of lncRNA H19 significantly downregulated the expression of autophagy markers, which is consistent with the results of autophagy-related protein changes detected in mouse femurs by immunofluorescence. CONCLUSION Appropriate treadmill exercise can effectively stimulate bone formation and promote the increase of bone density and bone volume in growing mice, thus enhancing the peak bone mass of mice. The lncRNA H19/miR-149 axis plays an important regulatory role in osteogenic differentiation.
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