Meng Xianmin, Wang Wenjie, Wang Xueling
Department of Stomatology, Aerospace Center Hospital, Beijing, PR China.
J Dent Sci. 2022 Jul;17(3):1281-1291. doi: 10.1016/j.jds.2021.11.011. Epub 2021 Dec 6.
BACKGROUND/PURPOSE: During orthodontic tooth movement, mechanical forces induce the osteogenic differentiation of periodontal ligament stem cells (PDLSCs), which contributes to alveolar bone remodeling. MicroRNAs (miRNAs) are involved in regulating PDLSC osteogenic differentiation. Therefore, we intended to explore the role of miR-34a and miR-146a in osteogenic differentiation of PDLSCs under cyclic stretch.
Phenotypic identification of PDLSCs was determined by flow cytometry analysis. PDLSCs were incubated with osteogenic differentiation medium for 3 weeks and the osteogenic differentiation capability was detected by Alizarin Red staining. To mimic the orthodontic forces, cyclic mechanical stretch was applied to PDLSCs. Alkaline phosphatase (ALP) activity assay and ALP staining were used for evaluating the ALP activity. The expression of osteogenesis markers in PDLSCs was assessed by western blotting and qRT-PCR. The binding between miR-34a (or miR-146a) and CUGBP Elav-like family member 3 (CELF3) was validated by luciferase reporter assay.
Cyclic stretch elevated ALP activity and the expression of osteogenesis markers, osteopontin (OPN), runt-related transcription factor 2 (RUNX2), type I collagen (COL1), ALP, osteocalcin (OCN) and osterix (OSX), in PDLSCs. MiR-146a and miR-34a were downregulated in PDLSCs under cyclic stretch. Either overexpressing miR-146a and miR-34a reduced ALP activity and the expression of osteogenesis markers. CELF3 was a target of both miR-146a and miR-34a. CELF3 silencing attenuated while CELF3 overexpression enhanced ALP activity and the expression of osteogenesis markers.
MiR-34a and miR-146a repress cyclic stretch-induced osteogenic differentiation of PDLSCs via regulating the expression of CELF3.
背景/目的:在正畸牙齿移动过程中,机械力诱导牙周膜干细胞(PDLSCs)的成骨分化,这有助于牙槽骨重塑。微小RNA(miRNAs)参与调节PDLSCs的成骨分化。因此,我们旨在探讨miR-34a和miR-146a在周期性拉伸下对PDLSCs成骨分化的作用。
通过流式细胞术分析确定PDLSCs的表型鉴定。将PDLSCs与成骨分化培养基孵育3周,并通过茜素红染色检测成骨分化能力。为模拟正畸力,对PDLSCs施加周期性机械拉伸。使用碱性磷酸酶(ALP)活性测定和ALP染色评估ALP活性。通过蛋白质印迹和qRT-PCR评估PDLSCs中成骨标志物的表达。通过荧光素酶报告基因测定验证miR-34a(或miR-146a)与CUGBP Elav样家族成员3(CELF3)之间的结合。
周期性拉伸提高了PDLSCs中ALP活性和成骨标志物骨桥蛋白(OPN)、 runt相关转录因子2(RUNX2)、I型胶原蛋白(COL1)、ALP、骨钙素(OCN)和osterix(OSX)的表达。在周期性拉伸下,PDLSCs中miR-146a和miR-34a表达下调。过表达miR-146a和miR-34a均可降低ALP活性和成骨标志物的表达。CELF3是miR-146a和miR-34a的靶标。CELF3沉默减弱而CELF3过表达增强ALP活性和成骨标志物的表达。
miR-34a和miR-146a通过调节CELF3的表达抑制周期性拉伸诱导的PDLSCs成骨分化。