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长链非编码RNA MALAT1通过调节miR-494/SP1轴增强骨再生过程中的血管生成。

Long non-coding RNA MALAT1 enhances angiogenesis during bone regeneration by regulating the miR-494/SP1 axis.

作者信息

Ding Ao, Li Cheng-Hua, Yu Chan-Yuan, Zhou Hang-Tian, Zhang Zhi-Hong

机构信息

Department of Stomatology, The First Affiliated Hospital of USTC (Anhui Provincial Hospital), Division of Life Sciences and Medicine, University of Science and Technology of China, Hefei, Anhui Province, P.R. China.

Department of Stomatology, Beidaihe Rihabilitation and Recuperation Center of PLA, Qinhuangdao, Hebei Province, P.R. China.

出版信息

Lab Invest. 2021 Nov;101(11):1458-1466. doi: 10.1038/s41374-021-00649-8. Epub 2021 Aug 14.

Abstract

Bone regeneration is a coordinated process involving connections between blood vessels and osteocytes. Angiogenesis and osteogenesis are tightly connected throughout the progression of bone regeneration. This study aimed to explore the underlying mechanism of metastasis-associated lung adenocarcinoma transcript 1 (MALAT1)-regulated angiogenesis during bone regeneration. Gene and protein expression was detected by quantitative real-time PCR and western blot assay. Vascular endothelial growth factor (VEGFA) secretion was assessed by enzyme-linked immunosorbent assay. To evaluate the effect of osteogenic differentiation, alkaline phosphatase (ALP) and alizarin red staining assays were performed. Proliferation was detected by 3-(4,5-Dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide assay. Migration and angiogenesis were measured using Transwell and tube formation assays. A dual luciferase reporter assay was performed to confirm the binding relationship among MALAT1, miR-494, and specificity protein 1 (SP1). Expression levels of MALAT1, SP1, and VEGFA were elevated and miR-494 was suppressed in MC3T3-E1 cells after culture in osteogenic medium. MALAT1 knockdown suppressed the osteogenic differentiation of MC3T3-E1, since ALP activity, mineralized nodules, and expression of the osteodifferentiated markers runt-related transcription factor 2 and osterix were restrained. In addition, MALAT1 silencing inhibited angiogenesis during bone regeneration, as the proliferation, migration, and capillary tube formation of human umbilical vein endothelial cells were blocked. Furthermore, miR-494 was directly targeted by MALAT1 and regulated the SP1/Toll-like receptor 2 (TLR2)/bone morphogenetic protein 2 (BMP2) axis by targeting SP1. Furthermore, miR-494 overexpression inhibited angiogenesis and osteogenic differentiation. Moreover, SP1 overexpression or miR-494 inhibition rescued the regulatory effect of sh-MALAT1 on angiogenesis and osteogenic differentiation. Taken together, these findings indicate that MALAT1 promotes angiogenesis and osteogenic differentiation by targeting miR-494 and activating the SP1/TLR2/BMP2 pathway, suggesting a novel target for bone regeneration therapy by promoting angiogenesis.

摘要

骨再生是一个涉及血管与骨细胞之间联系的协调过程。在骨再生的整个进程中,血管生成和成骨作用紧密相连。本研究旨在探索转移相关肺腺癌转录本1(MALAT1)在骨再生过程中调控血管生成的潜在机制。通过定量实时聚合酶链反应和蛋白质免疫印迹法检测基因和蛋白质表达。采用酶联免疫吸附测定法评估血管内皮生长因子(VEGFA)的分泌。为评估成骨分化的效果,进行了碱性磷酸酶(ALP)和茜素红染色试验。通过3-(4,5-二甲基噻唑-2-基)-2,5-二苯基四氮唑溴盐试验检测细胞增殖。使用Transwell和小管形成试验测量细胞迁移和血管生成。进行双荧光素酶报告基因试验以确认MALAT1、miR-494和特异性蛋白1(SP1)之间的结合关系。在成骨培养基中培养后,MC3T3-E1细胞中MALAT1、SP1和VEGFA的表达水平升高,而miR-494受到抑制。敲低MALAT1可抑制MC3T3-E1细胞的成骨分化,因为碱性磷酸酶活性、矿化结节以及成骨分化标志物 runt相关转录因子2和osterix的表达均受到抑制。此外,沉默MALAT1可抑制骨再生过程中的血管生成,因为人脐静脉内皮细胞的增殖、迁移和毛细血管管形成均被阻断。此外,miR-494是MALAT1的直接靶点,并通过靶向SP1调控SP1/Toll样受体2(TLR2)/骨形态发生蛋白2(BMP2)轴。此外,miR-494过表达可抑制血管生成和成骨分化。此外,SP1过表达或miR-494抑制可挽救sh-MALAT1对血管生成和成骨分化的调控作用。综上所述,这些发现表明MALAT1通过靶向miR-494并激活SP1/TLR2/BMP2途径促进血管生成和成骨分化,提示通过促进血管生成进行骨再生治疗的新靶点。

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