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miR-29a-5p 靶向 SATB2 并调控 SIRT1/Smad3 去乙酰化通路抑制胸椎黄韧带细胞成骨。

miR-29a-5p Targets SATB2 and Regulates the SIRT1/Smad3 Deacetylation Pathway to Inhibit Thoracic Ligamentum Flavum Cell Osteogenesis.

机构信息

Department of Orthopedics, Zhejiang Provincial People's Hospital, People's Hospital of Hangzhou Medical College, Hangzhou, PR China.

Department of Endocrinology, Affiliated Hangzhou First People's Hospital, Zhejiang University School of Medicine, Hangzhou, PR China.

出版信息

Spine (Phila Pa 1976). 2020 Sep 1;45(17):E1057-E1065. doi: 10.1097/BRS.0000000000003505.

Abstract

STUDY DESIGN

Experimental analysis of the thoracic ligamentum flavum cell osteogenic differentiation process.

OBJECTIVE

This study aimed to explore the role of miR-29a-5p and special AT-rich sequence-binding protein 2 (SATB2) in a pathological osteogenic process.

SUMMARY OF BACKGROUND DATA

Thoracic ossification of the ligamentum flavum (TOLF) is an uncommon disease wherein ligaments within the spine undergo progressive ossification, resulting in stenosis of the spinal canal and myelopathy. MiR-29a-5p was found to be downregulated in ligament cells from ossified ligament tissue in a previous study. However, whether miR-29a-5p is involved in the process of TOLF has not been investigated.

METHODS

The expression of miR-29a-5p in ligament tissues or in the context of TOLF osteogenic cell differentiation was measured via qRT-PCR. Alkaline phosphatase activity assay and Alizarin red staining were used to analyze cellular osteogenesis. The protein-level expression of SATB2, SIRT1, and Smad3 were measured via immunohistochemistry or western blotting. Dual luciferase reporter assays and western blotting were used to confirm that miR-29a targets SATB2.

RESULTS

SATB2 was found to be upregulated and miR-29a-5p was downregulated in TOLF tissue. We additionally observed decreased miR-29a-5p expression during the process of TOLF osteogenic cell differentiation, and there was a marked reduction in the expression of key mediators of osteogenesis when miR-29a-5p was overexpressed. Consistent with this, when miR-29a-5p was inhibited this led to enhanced osteogenic cell differentiation of these cells. We further found miR-29a-5p to directly target and suppress the expression of SATB2. Knock-down of SATB2 was sufficient to reduce the ability of miR-29a-5p to inhibit osteogenesis, and this also led to decreased SIRT1 expression and Smad3 acetylation.

CONCLUSION

Together our findings indicate that miR-29a-5p is able to prevent thoracic ligamentum flavum cell osteogenesis at least in part via targeting SATB2 and thereby suppressing the SIRT1/Smad3 deacetylation pathway.

LEVEL OF EVIDENCE

N/A.

摘要

研究设计

胸韧带黄细胞成骨分化过程的实验分析。

目的

本研究旨在探讨 miR-29a-5p 和特殊富含 AT 的序列结合蛋白 2(SATB2)在病理性成骨过程中的作用。

背景资料概要

胸韧带黄骨化(TOLF)是一种不常见的疾病,脊柱中的韧带会发生进行性骨化,导致椎管狭窄和脊髓病。在之前的研究中发现,miR-29a-5p 在骨化韧带组织中的韧带细胞中表达下调。然而,miR-29a-5p 是否参与 TOLF 过程尚未得到研究。

方法

通过 qRT-PCR 测量 miR-29a-5p 在韧带组织或 TOLF 成骨细胞分化过程中的表达。碱性磷酸酶活性测定和茜素红染色用于分析细胞成骨作用。通过免疫组织化学或 Western blot 测量 SATB2、SIRT1 和 Smad3 的蛋白水平表达。双荧光素酶报告基因检测和 Western blot 用于证实 miR-29a 靶向 SATB2。

结果

在 TOLF 组织中发现 SATB2 上调和 miR-29a-5p 下调。我们还观察到在 TOLF 成骨细胞分化过程中 miR-29a-5p 表达降低,并且当 miR-29a-5p 过表达时,成骨关键介质的表达明显降低。与此一致的是,当 miR-29a-5p 被抑制时,这些细胞的成骨细胞分化增强。我们进一步发现 miR-29a-5p 可直接靶向并抑制 SATB2 的表达。SATB2 的敲低足以减少 miR-29a-5p 抑制成骨的能力,这也导致 SIRT1 表达减少和 Smad3 乙酰化。

结论

综上所述,我们的研究结果表明,miR-29a-5p 至少部分通过靶向 SATB2 抑制 SIRT1/Smad3 去乙酰化途径来防止胸韧带黄细胞成骨。

证据水平

无。

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