流体切应力诱导的 miR-146a-5p 下调通过靶向 SMAD4 抑制成骨细胞凋亡。
Fluid shear stress-induced down-regulation of miR-146a-5p inhibits osteoblast apoptosis via targeting SMAD4.
机构信息
Department of Orthopaedics, Lanzhou University Second Hospital, Lanzhou Gansu, China.
出版信息
Physiol Res. 2022 Dec 16;71(6):835-848. doi: 10.33549/physiolres.934922. Epub 2022 Oct 13.
Fluid shear stress (FSS) plays an important role in osteoblast apoptosis. However, the role of miRNA in osteoblast apoptosis under FSS and possible molecular mechanisms remain unknown. Our aim of the study was to explore whether miR-146a-5p regulates osteoblast apoptosis under FSS and its molecular mechanisms. FSS could down-regulate the expression of miR-146a-5p in MC3T3-E1 cells. We confirm that up-regulation of miR-146a-5p promotes osteoblasts apoptosis and down-regulation of miR-146a-5p inhibits osteoblasts apoptosis. We further demonstrated that FSS inhibits osteoblast apoptosis by down-regulated miR-146a-5p. Dual-luciferase reporter assay validated that SMAD4 is a direct target gene of miR-146a-5p. In addition, mimic-146a-5p suppressed FSS-induced up-regulation of SMAD4 protein levels, which suggests that FSS elevated SMAD4 protein expression levels via regulation miR-146a-5p. Further investigations showed that SMAD4 could inhibit osteoblast apoptosis. We demonstrated that miR-146a-5p regulates osteoblast apoptosis via targeting SMAD4. Taken together, our present study showed that FSS-induced down-regulation miR-146a-5p inhibits osteoblast apoptosis via target SMAD4. These findings may provide novel mechanisms for FSS to inhibit osteoblast apoptosis, and also may provide a potential therapeutic target for osteoporosis.
流体切应力 (FSS) 在成骨细胞凋亡中起重要作用。然而,miRNA 在 FSS 下成骨细胞凋亡中的作用及其可能的分子机制尚不清楚。本研究旨在探讨 miR-146a-5p 是否在 FSS 下调节成骨细胞凋亡及其分子机制。FSS 可下调 MC3T3-E1 细胞中 miR-146a-5p 的表达。我们证实上调 miR-146a-5p 可促进成骨细胞凋亡,而下调 miR-146a-5p 可抑制成骨细胞凋亡。我们进一步证明 FSS 通过下调 miR-146a-5p 抑制成骨细胞凋亡。双荧光素酶报告基因实验验证了 SMAD4 是 miR-146a-5p 的直接靶基因。此外,miR-146a-5p 模拟物抑制了 FSS 诱导的 SMAD4 蛋白水平的上调,这表明 FSS 通过调节 miR-146a-5p 升高了 SMAD4 蛋白表达水平。进一步的研究表明,SMAD4 可抑制成骨细胞凋亡。我们证明 miR-146a-5p 通过靶向 SMAD4 调节成骨细胞凋亡。综上所述,本研究表明 FSS 诱导的 miR-146a-5p 下调通过靶向 SMAD4 抑制成骨细胞凋亡。这些发现可能为 FSS 抑制成骨细胞凋亡提供新的机制,并为骨质疏松症提供潜在的治疗靶点。
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