Qiao Wenlan, Li Dong, Shi Qing, Wang Huanhuan, Wang Hao, Guo Jing
Shandong Provincial Key Laboratory of Oral Tissue Regeneration, Department of Orthodontics, School of Stomatology, Shandong University, Jinan, Shandong 250012, P.R. China.
Department of Stomatology, Qilu Hospital, and Institute of Stomatology, Shandong University, Jinan, Shandong 250012, P.R. China.
Exp Ther Med. 2020 Jan;19(1):9-18. doi: 10.3892/etm.2019.8213. Epub 2019 Nov 18.
Dental pulp stem cells (DPSCs) are reported to be enriched in stem/progenitor cells, however to the best of our knowledge they have yet to be well documented and characterized. In the present study, in order to characterize DPSCs and the effect of microRNAs (miRs/miRNAs) on DPSC properties, a miRNA array was performed between dental periodontal ligament cells (DPLCs) and DPSCs. The results revealed that miR-224-5p (miR-224) was highly expressed in the DPSCs compared with that in the DPLCs. The transfection of DPSCs with an miR-224 inhibitor impaired cell viability. In addition, miR-224 inhibition significantly promoted cell apoptosis in DPSCscompared with the NC group. analysis and a dual-luciferase reporter assay demonstrated that miR-224 targets the 3'-untranslated region of the Rac family small GTPase 1 (Rac1) gene. miR-224 downregulation resulted in the increased expression of Rac1 in DPSCs compared with DPLCs. Furthermore, miR-224 inhibition caused augmented mitogen-activated protein kinase 8, caspase-3, caspase-9 and Fas ligand expression in DPSC, which may be recovered by Rac1 silencing with transfection with short hairpin RNA-Rac1. Furthermore, Annexin V-fluorescein isothiocyanate/propidium iodide flow cytometry indicated that the silencing of Rac1 restored the pro-apoptotic DPSC cell number with miR-224 transfection. Therefore, the results of the present study suggested miR-224 in DPSC serves an important function in protecting cells against apoptosis by downregulating Rac1 expression, and also identified miR-224 as a novel miRNA in regulating the features of DPSC.
据报道,牙髓干细胞(DPSCs)富含干/祖细胞,然而据我们所知,它们尚未得到充分的记录和表征。在本研究中,为了表征DPSCs以及微小RNA(miRs/miRNAs)对DPSC特性的影响,在牙周膜细胞(DPLCs)和DPSCs之间进行了miRNA阵列分析。结果显示,与DPLCs相比,miR-224-5p(miR-224)在DPSCs中高表达。用miR-224抑制剂转染DPSCs会损害细胞活力。此外,与NC组相比,抑制miR-224可显著促进DPSCs中的细胞凋亡。分析和双荧光素酶报告基因检测表明,miR-224靶向Rac家族小GTP酶1(Rac1)基因的3'-非翻译区。与DPLCs相比,miR-224下调导致DPSCs中Rac1表达增加。此外,抑制miR-224会导致DPSC中有丝分裂原激活蛋白激酶8、半胱天冬酶-3、半胱天冬酶-9和Fas配体表达增加,而用短发夹RNA-Rac1转染使Rac1沉默可恢复这些增加的表达。此外,膜联蛋白V-异硫氰酸荧光素/碘化丙啶流式细胞术表明,Rac1沉默可恢复miR-224转染导致的促凋亡DPSC细胞数量。因此,本研究结果表明,DPSC中的miR-224通过下调Rac1表达在保护细胞免受凋亡方面发挥重要作用,并且还将miR-224鉴定为调节DPSC特性的一种新型miRNA。