Hsa_Circ_0005044通过调节miR-296-3p/FOSL1促进牙髓干细胞成骨/成牙分化

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS ACS Applied Bio Materials Pub Date : 2023-01-01 DOI:10.1089/dna.2022.0394
Zhongjun Liu, Siwei Li, Shuaimei Xu, Nu Er Bi Ya A Bu Du Xi Ku, Jun Wen, Xiongqun Zeng, Xiaoqing Shen, Pingping Xu
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引用次数: 0

摘要

环状rna (circRNAs)是一种缺乏编码潜能的rna。这些环状rna在牙髓干细胞(DPSC)成骨/牙源性分化中的作用仍有待确定。在本研究中,通过RNA-seq分析了DPSC成骨/牙源性分化过程中的circRNA表达谱。采用qRT-PCR证实circ_0005044、miR-296-3p和FOSL1在DPSC成骨分化过程中的差异表达。Circ_0005044、miR-296-3p和FOSL1被敲低或过表达。通过碱性磷酸酶(ALP)和茜素红S (ARS)染色检测成骨细胞活性和相关矿物质活性。通过荧光素酶报告基因检测评估miR-296-3p、circ_0005044和FOSL1之间的相互作用。最后,利用体内系统证实circ_0005044与成骨细胞分化的相关性。结果,我们在DPSC成骨/牙源性分化过程中检测到显著的circ_0005044和FOSL1上调,以及伴随的miR-296-3p下调。当敲除circ_0005044或过表达miR-296-3p时,可显著抑制成骨。荧光素酶报告基因检测证实miR-296-3p能够结合circ_0005044和FOSL1野生型中的保守序列。此外,在体内敲除circ_0005044显著减弱骨形成。因此,circ_0005044/miR-2964-3p/FOSL1轴调控DPSC成骨/牙源性分化,可能为牙髓复合体再生提供潜在的分子靶点。
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Hsa_Circ_0005044 Promotes Osteo/Odontogenic Differentiation of Dental Pulp Stem Cell Via Modulating miR-296-3p/FOSL1.

Circular RNAs (circRNAs) are a form of RNAs that lack coding potential. The role of such circRNAs in dental pulp stem cell (DPSC) osteo/odontogenic differentiation remains to be determined. In this study, circRNA expression profiles in DPSC osteo/odontogenic differentiation process were analyzed by RNA-seq. qRT-PCR was used to confirm the differential expression of circ_0005044, miR-296-3p, and FOSL1 in DPSC osteogenic differentiation process. Circ_0005044, miR-296-3p, and FOSL1 were knocked down or overexpressed. Osteoblastic activity and associated mineral activity were monitored via alkaline phosphatase (ALP) and alizarin red S (ARS) staining. Interactions between miR-296-3p, circ_0005044, and FOSL1 were assessed through luciferase reporter assays. Finally, an in vivo system was used to confirm the relevance of circ_0005044 to osteoblastic differentiation. As results, we detected significant circ_0005044 and FOSL1 upregulation in DPSC osteo/odontogenic differentiation process, as well as concomitant miR-296-3p downregulation. When knocking down circ_0005044 or overexpressed miR-296-3p, this significantly inhibited osteogenesis. Luciferase reporter assay confirmed that miR-296-3p was capable of binding to conserved sequences in the wild-type forms of both the circ_0005044 and FOSL1. Furthermore, knocking down circ_0005044 in vivo significantly attenuated bone formation. Therefore, the circ_0005044/miR-2964-3p/FOSL1 axis regulates DPSC osteo/odontogenic differentiation, which may provide potential molecular targets for dental-pulp complex regeneration.

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ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
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