机构:[a]Laboratory of Tissue Regeneration and Immunology and Department of Periodontics, Beijing Key Laboratory of Tooth Regeneration and Function Reconstruction, School of Stomatology, Capital Medical University, PR China[b]Department of Orthodontics School of Stomatology, Capital Medical University, PR China[c]Department of Stomatology, Beijing Tiantan Hospital, Capital Medical University, PR China首都医科大学附属天坛医院[d]Salivary Gland Disease Center and Molecular Laboratory for Gene Therapy and Tooth Regeneration, School of Stomatology, Capital Medical University, PR China
Wound healing is regulated by a complex network of cells, molecules, and cytokines, as well as microRNAs (miRNAs). miRNAs were confirmed to influence the wound healing process, and miR-21, an important member of the miRNA family, was also shown to regulate wound healing. The aim of the present study was to investigate the role of miR-21 in the wound healing process and the possible underlying cell signaling pathways. We isolated GMSCs from WT and miR-21-KO mouse gingiva. Flow cytometric analysis and immunocytofluorescense staining were used to identify the GMSCs acquired from WT and miR-21-KO mice. RT-PCR, western blot analysis and immunohistofluorescence staining were performed to examine the expression of extracellular matrix components and key proteins of cell signaling pathways. TargetScan and pmiR-RB-REPORT vectors were used to verify that Smad7 was a direct target of miR-21. Compared to WT mice, miR-21-KO mice showed slower wound healing. RT-PCR and western blot analysis indicated that Elastin expression was downregulated in miR-21-deficient samples. We confirmed that Smad7 was a direct target of miR-21. miR-21 knockout resulted in increased expression of Smad7 and impaired phosphorylation of the Smad2/3 complex. The expression of the Smad7-Smad2/3-Elastin axis in palate tissues sections acquired from WT and miR-21-KO mice showed the same trend. Based on all these results, we demonstrated that miR-21 promoted the wound healing process via the Smad7-Smad2/3-Elastin pathway.
基金:
National Natural Science Foundation of ChinaNational Natural Science Foundation of China [81470751, 81222011, 81600891, 81470759]; Natural Science Foundation of Shandong ProvinceNatural Science Foundation of Shandong Province [ZR2015HL055]; Beijing Municipal Administration of Hospitals Clinical Medicine Development [ZYLX201703]
第一作者机构:[a]Laboratory of Tissue Regeneration and Immunology and Department of Periodontics, Beijing Key Laboratory of Tooth Regeneration and Function Reconstruction, School of Stomatology, Capital Medical University, PR China
通讯作者:
通讯机构:[a]Laboratory of Tissue Regeneration and Immunology and Department of Periodontics, Beijing Key Laboratory of Tooth Regeneration and Function Reconstruction, School of Stomatology, Capital Medical University, PR China[c]Department of Stomatology, Beijing Tiantan Hospital, Capital Medical University, PR China
推荐引用方式(GB/T 7714):
Xiaoyan Li,Lijia Guo,Yitong Liu,et al.MicroRNA-21 promotes wound healing via the Smad7-Smad2/3-Elastin pathway[J].EXPERIMENTAL CELL RESEARCH.2018,362(2):245-251.doi:10.1016/j.yexcr.2017.11.019.
APA:
Xiaoyan Li,Lijia Guo,Yitong Liu,Yingying Su,Yongmei Xie...&Yi Liu.(2018).MicroRNA-21 promotes wound healing via the Smad7-Smad2/3-Elastin pathway.EXPERIMENTAL CELL RESEARCH,362,(2)
MLA:
Xiaoyan Li,et al."MicroRNA-21 promotes wound healing via the Smad7-Smad2/3-Elastin pathway".EXPERIMENTAL CELL RESEARCH 362..2(2018):245-251