JNK通路在低频脉冲电磁场促进牙周膜干细胞成骨分化中的作用
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R783.1

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上海市卫生和计划生育委员会科研课题(20134418),解放军总后勤部面上项目(CHJ13J035),海军军医大学(第二军医大学)第一附属医院青年启动基金(2019QN16),海军军医大学(第二军医大学)第一附属医院“234学科攀峰计划”(2020YXK028),海军军医大学(第二军医大学)第一附属医院教改项目(CHJG2020040).


Role of JNK pathway in osteogenic differentiation of periodontal ligament stem cells stimulated by low-frequency pulsed electromagnetic fields
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Supported by Scientific Research Project of Shanghai Municipal Commission of Health and Family Planning (20134418), General Program of Logistics Department of PLA (CHJ13J035), and Youth Initial Fund (2019QN16), the "234 Discipline Peak Climbing Plan" (2020YXK028) and Education Reform Project of The First Affiliated Hospital of Naval Medical University (Second Milltary Medical University) (CHJG2020040).

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    摘要:

    目的 通过c-Jun氨基末端激酶(JNK)特异性抑制剂SP600125干预JNK信号通路,探究JNK通路是否参与低频脉冲电磁场(PEMF)诱导人牙周膜干细胞(hPDLSC)的成骨分化。方法 用低频PEMF(15 Hz、0~3 mT、每间隔12 h辐照1 h)体外辐照hPDLSC,第7天或第14天时通过qPCR检测细胞内Runt相关转录因子2(Runx2)、碱性磷酸酶(ALP)、骨桥蛋白(OPN)、骨钙蛋白(OCN)等成骨相关基因表达水平,评估低频PEMF诱导hPDLSC成骨分化的能力并筛选适宜的磁场作用强度;通过蛋白质印迹法检测低频PEMF刺激下细胞内JNK和磷酸化JNK(p-JNK)蛋白表达水平,qPCR检测不同浓度SP600125干预后细胞内成骨相关基因表达水平的变化,观察JNK通路在PEMF促进hPDLSC成骨分化过程中是否发挥作用。结果 hPDLSC经15 Hz、2.5 mT的低频PEMF辐照后,Runx2、ALP、OPN、OCN等成骨相关基因表达水平高于其他磁场强度分组(P均<0.05)。低频PEMF刺激下明显促进了细胞内JNK、p-JNK蛋白的表达(P均<0.05);JNK通路抑制后细胞内成骨相关基因表达水平降低,且20、30 μmol/L SP600125对成骨基因表达的抑制效果较10 μmol/L SP600125更明显(P均<0.05)。结论 15 Hz、2.5 mT的PEMF可通过部分激活JNK通路诱导hPDLSC成骨分化。

    Abstract:

    Objective To explore whether c-Jun N-terminal kinase (JNK) pathway is involved in the osteogenic differentiation of human periodontal ligament stem cells (hPDLSCs) induced by low-frequency pulsed electromagnetic field (PEMF) via using the specific inhibitor SP600125 to intervene JNK signaling pathway. Methods hPDLSCs were exposed to the low-frequency PEMF stimulation (15 Hz, 0-3.0 mT, radiate for 1 h every 12 h) in vitro for 7 d or 14 d and the expression levels of osteogenic-related genes Runt-related transcription factor 2 (Runx2), alkaline phosphatase (ALP), osteopontin (OPN) and osteocalcin (OCN) were detected by quantitative polymerase chain reaction (qPCR), so as to determine the osteogenic differentiation ability of cells induced by low-frequency PEMF and the appropriate magnetic field intensity. To determine whether JNK pathway plays a role in the osteogenic differentiation of hPDLSCs stimulated by low-frequency PEMF, the expression levels of JNK and phosphorylated-JNK (p-JNK) proteins were detected by Western blotting; and the expression levels of osteogenic genes in cells treated with different concentrations of SP600125 were detected by qPCR. Results The expression levels of osteogenic-related genes Runx2, ALP, OPN and OCN were higher in hPDLSCs irradiated with low-frequency PEMF at 15 Hz and 2.5 mT than other intensity groups (all P<0.05). Low-frequency PEMF significantly stimulated the expression of JNK and p-JNK proteins in cells (both P<0.05). The expression levels of osteogenic genes in hPDLSCs were decreased after the JNK pathway was inhibited by SP600125, and the inhibitory effects of 20 and 30 μmol/L SP600125 were more obvious than that of 10 μmol/L SP600125 (both P<0.05). Conclusion PEMF (15 Hz,2.5 mT) partially activates JNK pathway to induce hPDLSC osteogenic differentiation.

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  • 收稿日期:2022-04-30
  • 最后修改日期:2022-11-21
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  • 在线发布日期: 2023-03-30
  • 出版日期: 2023-03-20
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