留言板

尊敬的读者、作者、审稿人, 关于本刊的投稿、审稿、编辑和出版的任何问题, 您可以本页添加留言。我们将尽快给您答复。谢谢您的支持!

姓名
邮箱
手机号码
标题
留言内容
验证码

褪黑素调控Nrf2/ARE信号通路延缓髓核间充质干细胞退变的实验研究

李才 许盼盼 胡捷 朱坤 叶雨辰 张亚伟 张长春

李才, 许盼盼, 胡捷, 朱坤, 叶雨辰, 张亚伟, 张长春. 褪黑素调控Nrf2/ARE信号通路延缓髓核间充质干细胞退变的实验研究[J]. 中华全科医学, 2022, 20(11): 1831-1835. doi: 10.16766/j.cnki.issn.1674-4152.002713
引用本文: 李才, 许盼盼, 胡捷, 朱坤, 叶雨辰, 张亚伟, 张长春. 褪黑素调控Nrf2/ARE信号通路延缓髓核间充质干细胞退变的实验研究[J]. 中华全科医学, 2022, 20(11): 1831-1835. doi: 10.16766/j.cnki.issn.1674-4152.002713
LI Cai, XU Pan-pan, HU Jie, ZHU Kun, YE Yu-chen, ZHANG Ya-wei, ZHANG Chang-chun. Melatonin regulates Nrf2/ARE signal pathway to delay the degeneration of nucleus pulposus mesenchymal stem cells[J]. Chinese Journal of General Practice, 2022, 20(11): 1831-1835. doi: 10.16766/j.cnki.issn.1674-4152.002713
Citation: LI Cai, XU Pan-pan, HU Jie, ZHU Kun, YE Yu-chen, ZHANG Ya-wei, ZHANG Chang-chun. Melatonin regulates Nrf2/ARE signal pathway to delay the degeneration of nucleus pulposus mesenchymal stem cells[J]. Chinese Journal of General Practice, 2022, 20(11): 1831-1835. doi: 10.16766/j.cnki.issn.1674-4152.002713

褪黑素调控Nrf2/ARE信号通路延缓髓核间充质干细胞退变的实验研究

doi: 10.16766/j.cnki.issn.1674-4152.002713
基金项目: 

安徽省自然科学重点项目 1908085MC90

安徽省教育厅自然科学重点项目 KJ2021A0743

蚌埠医学院研究生科研创新计划 Byycx20029

蚌埠医学院大学生创新创业训练计划 bydc2021017

详细信息
    通讯作者:

    张长春,E-mail:zccanhui@sina.com

  • 中图分类号: R681.53 R-332

Melatonin regulates Nrf2/ARE signal pathway to delay the degeneration of nucleus pulposus mesenchymal stem cells

  • 摘要:   目的  探讨褪黑素对氧化应激条件下的大鼠髓核间充质干细胞(NPMSCs)的影响及调节机制。  方法  使用差速贴壁法获取大鼠NPMSCs。显微镜下观察细胞状态,鉴定第三代细胞三系分化潜能和细胞表面免疫标志物;采用CCK-8法检测不同浓度过氧化氢和褪黑素诱导对大鼠NPMSCs活力的影响确定最佳浓度和实验分组;免疫荧光和流式细胞学技术检测NPMSCs活性氧水平;免疫印迹分析外基质标志蛋白(Ⅱ型胶原、糖胺聚糖)和通路核心蛋白(Nrf2、HO-1)表达情况。  结果  褪黑素在氧化应激下保护了NPMSCs的活性,且1 μmol/L浓度保护效应最为明显(0.717±0.018,t=7.102, P<0.01)。褪黑素可抑制NPMSCs在H2O2诱导后的活性氧水平(阳性率70.0% vs. 32.7%)。此外,褪黑素还能显著提高Nrf2/ARE信号通路中关键蛋白核因子E2相关因子(1.925±0.024,t=13.150,P<0.01)和血红素氧合酶-1(1.605±0.019,t=12.940, P<0.01)的活性,改善NPMSCs的功能。褪黑素治疗后,细胞基质蛋白Ⅱ型胶原(0.850±0.010,t=25.200,P<0.01)和糖胺聚糖(0.335±0.013,t=10.640,P<0.01)表达增加。  结论  褪黑素通过调控Nrf2/ARE信号通路可以影响NPMSCs退变的生物学特性。

     

  • 图  1  NPMSCs表型鉴定

    注:A为第3代NPMSCs细胞形态观察(×100);B~D为28 d诱导后茜素红染色、油红O染色和阿利辛蓝染色(×100);E为流式检测显示细胞高表达CD73、CD90,低表达CD34、CD45。

    Figure  1.  Phenotypic identification of NPMSCs

    图  2  褪黑素和H2O2对NPMSCs增殖的影响

    注: A为不同浓度褪黑素对NPMSCs的细胞毒性检测;B为不同浓度H2O2和褪黑素预处理后诱导下细胞活力检测。与对照组比较,aP < 0.01;与H2O2组比较,bP < 0.01。

    Figure  2.  Effects of melatonin and H2O2 on proliferation of NPMSCs

    图  3  褪黑素改善NPMSCs氧化应激下的ROS水平

    注:A为不同处理组明场形态学观察(×100);B为不同处理组ROS在细胞内荧光分布(×100);C为各处理组ROS水平流式细胞学检测。

    Figure  3.  Melatonin improves Ros levels of NPMSCs under oxidative stress

    图  4  褪黑素激活Nrf2/ARE通路改善NPMSCs退变

    注:Western blotting检测各处理组外基质成分蛋白Ⅱ型胶原、糖胺聚糖及核蛋白Nrf2和下游靶蛋白HO-1相对表达水平;与对照组比较,aP < 0.01;与H2O2组比较,bP < 0.01。

    Figure  4.  Melatonin activates Nrf2/ARE pathway to ameliorate NPMSCs degeneration

  • [1] WILSON ZINGG R, KENDALL R. Obesity, vascular disease, and lumbar disk degeneration: Associations of comorbidities in low back pain[J]. PM R, 2017, 9(4): 398-402. doi: 10.1016/j.pmrj.2016.09.011
    [2] HUANG Y C, LEUNG V Y, LU W W, et al. The effects of microenvironment in mesenchymal stem cell-based regeneration of intervertebral disc[J]. Spine J, 2013, 13(3): 352-362. doi: 10.1016/j.spinee.2012.12.005
    [3] O'SULLIVAN K, O'SULLIVAN P B, KEEFFE M. The Lancet series on low back pain: Reflections and clinical implications[J]. Br J Sports Med, 2019, 53(7): 392-393. doi: 10.1136/bjsports-2018-099671
    [4] SHI R, WANG F, HONG X, et al. The presence of stem cells in potential stem cell niches of the intervertebral disc region: An in vitro study on rats[J]. Eur Spine J, 2015, 24(11): 2411-2424. doi: 10.1007/s00586-015-4168-7
    [5] QI L, WANG R, SHI Q, et al. Umbilical cord mesenchymal stem cell conditioned medium restored the expression of collagen Ⅱ and aggrecan in nucleus pulposus mesenchymal stem cells exposed to high glucose[J]. J Bone Miner Metab, 2019, 37(3): 455-466. doi: 10.1007/s00774-018-0953-9
    [6] NAN L P, WANG F, RAN D, et al. Naringin alleviates H2O2-induced apoptosis via the PI3K/Akt pathway in rat nucleus pulposus-derived mesenchymal stem cells[J]. Connect Tissue Res, 2020, 61(6): 554-567. doi: 10.1080/03008207.2019.1631299
    [7] BRZOZOWSKA I, STRZALKA M, DROZDOWICZ D, et al. Mechanisms of esophageal protection, gastroprotection and ulcer healing by melatonin. Implications for the therapeutic use of melatonin in gastroesophageal reflux disease (GERD) and peptic ulcer disease[J]. Curr Pharm Des, 2014, 20(30): 4807-4815. doi: 10.2174/1381612819666131119110258
    [8] LIM H D, KIM Y S, KO S H, et al. Cytoprotective and anti-inflammatory effects of melatonin in hydrogen peroxide-stimulated CHON-001 human chondrocyte cell line and rabbit model of osteoarthritis via the SIRT1 pathway[J]. J Pineal Res, 2012, 53(3): 225-237. doi: 10.1111/j.1600-079X.2012.00991.x
    [9] HAN Y C, LI X H, YAN M J, et al. Oxidative damage induces apoptosis and promotes calcification in disc cartilage endplate cell through ROS/MAPK/NF-κB pathway: Implications for disc degeneration[J]. Biochem Biophys Res Commun, 2019, 516(3): 1026-1032. doi: 10.1016/j.bbrc.2017.03.111
    [10] XU W N, ZHENG H L, YANG R Z, et al. Mitochondrial NDUFA4L2 attenuates the apoptosis of nucleus pulposus cells induced by oxidative stress via the inhibition of mitophagy[J]. Exp Mol Med, 2019, 51(11): 1-16.
    [11] LAZZARINI R, GUARNIERI S, FULGENZI G, et al. Mesenchymal stem cells from nucleus pulposus and neural differentiation potential: A continuous challenge[J]. J Mol Neurosci, 2019, 67(1): 111-124. doi: 10.1007/s12031-018-1216-x
    [12] HAN B, WANG H C, LI H, et al. Nucleus pulposus mesenchymal stem cells in acidic conditions mimicking degenerative intervertebral discs give better performance than adipose tissue-derived mesenchymal stem cells[J]. Cells Tissues Organs, 2014, 199(5-6): 342-352. doi: 10.1159/000369452
    [13] 马南, 耑冰, 李萍, 等. 氧化应激失衡在支气管哮喘急性发作中的意义[J]. 中华全科医学, 2019, 17(12): 1993-1997. doi: 10.16766/j.cnki.issn.1674-4152.001110

    MA N, ZHUAN B, LI P, et al. Significance of oxidative stress in acute exacerbation of bronchial asthma[J]. Chinese Journal of General Practice, 2019, 17(12): 1993-1997. doi: 10.16766/j.cnki.issn.1674-4152.001110
    [14] FAN P, YU X Y, XIE X H, et al. Mitophagy is a protective response against oxidative damage in bone marrow mesenchymal stem cells[J]. Life Sci, 2019, 229: 36-45. doi: 10.1016/j.lfs.2019.05.027
    [15] LI Z, LI X Y, CHEN C, et al. Melatonin inhibits nucleus pulposus (NP) cell proliferation and extracellular matrix (ECM) remodeling via the melatonin membrane receptors mediated PI3K-Akt pathway[J]. J Pineal Res, 2017. DOI: 10.1111/jpi.12435.
    [16] BAUER I, RAUPACH A. The Role of heme Oxygenase-1 in remote ischemic and anesthetic organ conditioning[J]. Antioxidants (Basel), 2019, 8(9): 403. doi: 10.3390/antiox8090403
  • 加载中
图(4)
计量
  • 文章访问数:  136
  • HTML全文浏览量:  36
  • PDF下载量:  4
  • 被引次数: 0
出版历程
  • 收稿日期:  2022-02-06
  • 网络出版日期:  2022-12-30

目录

    /

    返回文章
    返回