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周期性拉伸通过调节印度刺猬信号通路促进黄韧带骨化。

Cyclic stretch promotes the ossification of ligamentum flavum by modulating the Indian hedgehog signaling pathway.

机构信息

Department of Orthopedics, Changzheng Hospital, Second Military Medical University, Shanghai 200003, P.R. China.

Department of Orthopedics, Lanzhou General Hospital of PLA, Lanzhou, Gansu 730050, P.R. China.

出版信息

Mol Med Rep. 2020 Aug;22(2):1119-1128. doi: 10.3892/mmr.2020.11200. Epub 2020 Jun 2.

Abstract

The Indian hedgehog (IHH) signaling pathway is an important pathway for bone growth and development. The aim of the present study was to examine the role of the IHH signaling pathway in the development of the ossification of ligamentum flavum (OLF) at the cellular and tissue levels. The expression levels and localization of the osteogenic genes Runt-related transcription factor 2 (RUNX2), Osterix, alkaline phosphatase (ALP), osteocalcin (OCN) and IHH were evaluated in OLF tissues by reverse transcription-quantitative PCR (RT-qPCR) and immunohistochemistry. Non-ossified ligamentum flavum (LF) sections were used as control samples. The tissue explant method was used to obtain cultured LF cells. In addition, OLF cells were subjected to cyclic stretch application for 0, 6, 12 or 24 h. The expression levels of osteogenic genes, and the IHH signaling pathway genes IHH, Smoothened (SMO), GLI family zinc finger 1 (GLI1), GLI2 and GLI3 were evaluated with RT-qPCR and western blotting. Osteogenic differentiation was further evaluated by assessing ALP activity and staining. Moreover, the effect of cyclopamine (Cpn), an IHH signaling inhibitor, on osteogenic differentiation was examined. The RT-qPCR and immunohistochemical results indicated that the mRNA and protein expression levels of RUNX2, Osterix, ALP, OCN and IHH were significantly higher in the OLF group compared with the LF group. Furthermore, application of cyclic stretch to OLF cells resulted in greater ALP activity, and significant increases in mRNA and protein expression levels of RUNX2, Osterix, ALP and OCN in a time-d00ependent manner. Cyclic stretch application also led to significant increases in IHH signaling pathway genes, including IHH, SMO, GLI1 and GLI2, while no significant effect was found on GLI3 expression level. In addition, it was found that Cpn significantly reversed the effect of cyclic stretch on the ALP activity, and the expression levels of RUNX2, Osterix, ALP, OCN, GLI1 and GLI2. Collectively, the present results suggested that the IHH signaling pathway may mediate the effect of cyclic stretch on the OLF cells.

摘要

印度刺猬(IHH)信号通路是骨骼生长和发育的重要途径。本研究旨在从细胞和组织水平上探讨 IHH 信号通路在黄韧带骨化(OLF)发育中的作用。通过逆转录定量 PCR(RT-qPCR)和免疫组织化学方法评估 OLF 组织中成骨基因 runt 相关转录因子 2(RUNX2)、osterix、碱性磷酸酶(ALP)、骨钙素(OCN)和 IHH 的表达水平和定位。未骨化的黄韧带(LF)切片用作对照样本。采用组织外植体法获取培养的 LF 细胞。此外,对 OLF 细胞进行循环拉伸应用,持续 0、6、12 或 24 小时。通过 RT-qPCR 和 Western blot 评估成骨基因和 IHH 信号通路基因 IHH、Smoothened(SMO)、GLI 家族锌指蛋白 1(GLI1)、GLI2 和 GLI3 的表达水平。通过评估碱性磷酸酶(ALP)活性和染色进一步评估成骨分化。此外,还研究了 IHH 信号抑制剂环巴胺(Cpn)对成骨分化的影响。RT-qPCR 和免疫组织化学结果表明,与 LF 组相比,OLF 组 RUNX2、osterix、ALP、OCN 和 IHH 的 mRNA 和蛋白表达水平均显著升高。此外,循环拉伸应用于 OLF 细胞导致 ALP 活性显著增加,并且 RUNX2、osterix、ALP 和 OCN 的 mRNA 和蛋白表达水平随时间呈时间依赖性增加。循环拉伸应用还导致 IHH 信号通路基因,包括 IHH、SMO、GLI1 和 GLI2 的表达水平显著增加,而 GLI3 的表达水平没有显著影响。此外,还发现 Cpn 可显著逆转循环拉伸对 ALP 活性以及 RUNX2、osterix、ALP、OCN、GLI1 和 GLI2 表达水平的影响。综上所述,本研究结果提示,IHH 信号通路可能介导循环拉伸对 OLF 细胞的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ddc3/7339599/002a8c7cf2d6/MMR-22-02-1119-g00.jpg

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