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

应中央军委要求,2022年9月起,《药学实践杂志》将更名为《药学实践与服务》,双月刊,正文96页;2023年1月起,拟出版月刊,正文64页,数据库收录情况与原《药学实践杂志》相同。欢迎作者踊跃投稿!

巨噬源性泡沫细胞中p62蛋白上调作用和机制的研究

林张军 李倩 章越凡 芮耀诚

林张军, 李倩, 章越凡, 芮耀诚. 巨噬源性泡沫细胞中p62蛋白上调作用和机制的研究[J]. 药学实践与服务, 2019, 37(5): 400-405,426. doi: 10.3969/j.issn.1006-0111.2019.05.004
引用本文: 林张军, 李倩, 章越凡, 芮耀诚. 巨噬源性泡沫细胞中p62蛋白上调作用和机制的研究[J]. 药学实践与服务, 2019, 37(5): 400-405,426. doi: 10.3969/j.issn.1006-0111.2019.05.004
LIN Zhangjun, LI Qian, ZHANG Yuefan, RUI Yaocheng. A study on the role and mechanism of upregulated p62 protein in macrophage-derived foam cells[J]. Journal of Pharmaceutical Practice and Service, 2019, 37(5): 400-405,426. doi: 10.3969/j.issn.1006-0111.2019.05.004
Citation: LIN Zhangjun, LI Qian, ZHANG Yuefan, RUI Yaocheng. A study on the role and mechanism of upregulated p62 protein in macrophage-derived foam cells[J]. Journal of Pharmaceutical Practice and Service, 2019, 37(5): 400-405,426. doi: 10.3969/j.issn.1006-0111.2019.05.004

巨噬源性泡沫细胞中p62蛋白上调作用和机制的研究

doi: 10.3969/j.issn.1006-0111.2019.05.004
基金项目: 国家自然科学基金(30672455)

A study on the role and mechanism of upregulated p62 protein in macrophage-derived foam cells

  • 摘要: 目的 探讨巨噬源性泡沫细胞中p62蛋白对脂质代谢相关的自噬以及炎症因子表达的影响,为p62在抗动脉粥样硬化中的应用提供参考。 方法 利用Ox-LDL刺激RAW264.7细胞的方法模拟巨噬源性泡沫细胞的形成,通过Western blot及实时荧光定量PCR检测巨噬源性泡沫细胞中p62蛋白和mRNA水平。通过Western blot比较p62 siRNA组和对照组中Ox-LDL诱导的LC3剪切、脂滴相关蛋白Plin2和过氧化物酶体相关蛋白PEX2的蛋白水平,通过实时荧光定量PCR比较TNFα和IL-6 mRNA表达水平。 结果 Ox-LDL对RAW264.7细胞中p62蛋白以及mRNA水平均有上调作用。干扰p62的表达之后,LC3-Ⅱ蛋白水平降低,Plin2的蛋白水平并无明显变化,PEX2的蛋白水平升高,TNFα和IL-6 mRNA表达升高。进一步研究发现,干扰Nrf2后能明显抑制Ox-LDL对p62的上调作用。 结论 巨噬源性泡沫细胞中Ox-LDL通过Nrf2介导p62蛋白的上调,p62可能具有抗动脉粥样硬化的作用。
  • [1] HANSSON G K.Inflammation,atherosclerosis,and coronary artery disease[J].N Engl J Med,2005,352(16):1685-1695.
    [2] LEVINE B,KROEMER G.Autophagy in the pathogenesis of disease[J].Cell,2008,132(1):27-42.
    [3] EVANS T D,SERGIN I,ZHANG X Y,et al.Target acquired:Selective autophagy in cardiometabolic disease[J].Sci Signal,2017,10(468):eaag2298.
    [4] OUIMET M,FRANKLIN V,MAK E,et al.Autophagy regulates cholesterol efflux from macrophage foam cells via lysosomal acid lipase[J].Cell Metab,2011,13(6):655-667.
    [5] LIAO X H,SLUIMER J C,WANG Y,et al.Macrophage autophagy plays a protective role in advanced atherosclerosis[J].Cell Metab,2012,15(4):545-553.
    [6] LIPPAI M,LÖW P.The role of the selective adaptor p62 and ubiquitin-like proteins in autophagy[J].Biomed Res Int,2014,2014:832704.
    [7] MANLEY S,WILLIAMS J A,DING W X.Role of p62/SQSTM1 in liver physiology and pathogenesis[J].Exp Biol Med (Maywood),2013,238(5):525-538.
    [8] BITTO A,LERNER C A,NACARELLI T,et al.P62/SQSTM1 at the interface of aging,autophagy,and disease[J].Age (Dordr),2014,36(3):9626.
    [9] BURDELSKI C,REISWICH V,HUBE-MAGG C,et al.Cytoplasmic accumulation of sequestosome 1(p62) is a predictor of biochemical recurrence,rapid tumor cell proliferation,and genomic instability in prostate cancer[J].Clin Cancer Res,2015,21(15):3471-3479.
    [10] SERGIN I,BHATTACHARYA S,EMANUEL R,et al.Inclusion bodies enriched for p62 and polyubiquitinated proteins in macrophages protect against atherosclerosis[J].Sci Signal,2016,9(409):ra2.
    [11] SERGIN I,EVANS T D,ZHANG X Y,et al.Exploiting macrophage autophagy-lysosomal biogenesis as a therapy for atherosclerosis[J].Nat Commun,2017,8:15750.
    [12] GROOTAERT M O J,ROTH L,SCHRIJVERS D M,et al.Defective autophagy in atherosclerosis:to die or to senesce?[J].Oxid Med Cell Longev,2018,2018:7687083.
    [13] JEONG S J,ZHANG X Y,RODRIGUEZ-VELEZ A,et al.P62/SQSTM1 and selective autophagy in cardiometabolic diseases[J].Antioxid Redox Signal,2019,31(6):458-471.
    [14] HU D,WU J,XU L F,et al.A method for the establishment of a cell line with stable expression of the GFP-LC3 reporter protein[J].Mol Med Rep,2012,6(4):783-786.
    [15] LIU N,WU C M,SUN L Z,et al.Sesamin enhances cholesterol efflux in RAW264.7 macrophages[J].Molecules,2014,19(6):7516-7527.
    [16] GUPTA N,GOSWAMI R,ALHARBI M O,et al.TRPV 4 is a regulator in P.gingivalis lipopolysaccharide-induced exacerbation of macrophage foam cell formation[J].Physiol Rep,2019,7(7):e14069.
    [17] BIERMANNS M,VON LAAR J,BROSIUS U,et al.The peroxisomal membrane targeting elements of human peroxin 2(PEX2)[J].Eur J Cell Biol,2003,82(4):155-162.
    [18] ISHⅡ T,ITOH K,TAKAHASHI S,et al.Transcription factor Nrf2 coordinately regulates a group of oxidative stress-inducible genes in macrophages[J].J Biol Chem,2000,275(21):16023-16029.
    [19] PARK Y M.CD36,a scavenger receptor implicated in atherosclerosis[J].Exp Mol Med,2014,46:e99.DOI: 10.1038/emm.2014.38.
    [20] CHOROMANSKA B,MYSLIWIEC P,CHOROMANSKA K,et al.The role of CD36 receptor in the pathogenesis of atherosclerosis[J].Adv Clin Exp Med,2017,26(4):717-722.
    [21] JEONG S J,LEE M N,OH G T.The role of macrophage lipophagy in reverse cholesterol transport[J].Endocrinol Metab (Seoul),2017,32(1):41-46.
    [22] SANDA G M,DELEANU M,TOMA L,et al.Oxidized LDL-exposed human macrophages display increased MMP-9 expression and secretion mediated by endoplasmic reticulum stress[J].J Cell Biochem,2017,118(4):661-669.
    [23] YAO S T,MIAO C,TIAN H,et al.Endoplasmic reticulum stress promotes macrophage-derived foam cell formation by up-regulating cluster of differentiation 36(CD36) expression[J].J Biol Chem,2014,289(7):4032-4042.
    [24] NING H F,LIU D,YU X C,et al.Oxidized low-density lipoprotein-induced p62/SQSTM1 accumulation in THP-1-derived macrophages promotes IL-18 secretion and cell death[J].Exp Ther Med,2017,14(6):5417-5423.
    [25] KIM J Y,OZATO K.The sequestosome 1/p62 attenuates cytokine gene expression in activated macrophages by inhibiting IFN regulatory factor 8 and TNF receptor-associated factor 6/NF-kappaB activity[J].J Immunol,2009,182(4):2131-2140.
    [26] KIRKIN V,LAMARK T,JOHANSEN T,et al.NBR1 cooperates with p62 in selective autophagy of ubiquitinated targets[J].Autophagy,2009,5(5):732-733.
    [27] NIAN Z Q,SUN Z Q,YU L X,et al.Fat-specific protein 27 undergoes ubiquitin-dependent degradation regulated by triacylglycerol synthesis and lipid droplet formation[J].J Biol Chem,2010,285(13):9604-9615.
    [28] FUJIMOTO T,OHSAKI Y.Proteasomal and autophagic pathways converge on lipid droplets[J].Autophagy,2006,2(4):299-301.
    [29] OUIMET M,MARCEL Y L.Regulation of lipid droplet cholesterol efflux from macrophage foam cells[J].Arterioscler Thromb Vasc Biol,2012,32(3):575-581.
    [30] TILL A,LAKHANI R,BURNETT S F,et al.Pexophagy:the selective degradation of peroxisomes[J].Int J Cell Biol,2012,2012:512721.
    [31] SARGENT G,VAN ZUTPHEN T,SHATSEVA T,et al.PEX2 is the E3 ubiquitin ligase required for pexophagy during starvation[J].J Cell Biol,2016,214(6):677-690.
    [32] JAIN A,LAMARK T,SJØTTEM E,et al.P62/SQSTM1 is a target gene for transcription factor NRF2 and creates a positive feedback loop by inducing antioxidant response element-driven gene transcription[J].J Biol Chem,2010,285(29):22576-22591.
  • [1] 刘丽艳, 余小翠, 孙传铎.  纳武利尤单抗治疗非小细胞肺癌有效性及安全性的Meta分析 . 药学实践与服务, 2024, 42(): 1-6. doi: 10.12206/j.issn.2097-2024.202310044
    [2] 宋雨桐, 夏德润, 顾珩, 唐少文, 易洪刚, 沃红梅.  帕博利珠单抗与铂类化疗方案在晚期非小细胞肺癌一线治疗中的药物经济学评价 . 药学实践与服务, 2024, 42(7): 1-7. doi: 10.12206/j.issn.2097-2024.202303023
    [3] 冯志惠, 邓仪卿, 叶冰, 安培, 张宏, 张海军.  雀梅藤石油醚提取物诱导三阴性乳腺癌细胞凋亡的实验研究 . 药学实践与服务, 2024, 42(6): 253-259. doi: 10.12206/j.issn.2097-2024.202311055
    [4] 姜涛, 徐卫凡, 蒋益萍, 夏天爽, 辛海量.  巴戟天丸组方对Aβ损伤成骨细胞的作用及基于网络药理学的机制研究 . 药学实践与服务, 2024, 42(7): 285-290, 296. doi: 10.12206/j.issn.2097-2024.202305011
    [5] 杨媛媛, 安晓强, 许佳捷, 江键, 梁媛媛.  正极性驻极体联合5-氟尿嘧啶对瘢痕成纤维细胞生长抑制的协同作用 . 药学实践与服务, 2024, 42(6): 244-247. doi: 10.12206/j.issn.2097-2024.202310027
    [6] 毛智毅, 王筱燕, 陈晓颖, 汤逸斐.  度拉糖肽联合二甲双胍对肥胖型2型糖尿病患者机体代谢、体脂成分及血清脂肪因子的影响 . 药学实践与服务, 2024, 42(7): 305-309. doi: 10.12206/j.issn.2097-2024.202305032
    [7] 修建平, 杨朝爱, 刘禧澳, 潘乾禹, 韦广旭, 王卫星.  全反式维甲酸对肝星状细胞活化及氧化应激的作用和机制探索 . 药学实践与服务, 2024, 42(7): 1-6. doi: 10.12206/j.issn.2097-2024.202312054
  • 加载中
计量
  • 文章访问数:  3113
  • HTML全文浏览量:  367
  • PDF下载量:  393
  • 被引次数: 0
出版历程
  • 收稿日期:  2019-06-23
  • 修回日期:  2019-07-23

巨噬源性泡沫细胞中p62蛋白上调作用和机制的研究

doi: 10.3969/j.issn.1006-0111.2019.05.004
    基金项目:  国家自然科学基金(30672455)

摘要: 目的 探讨巨噬源性泡沫细胞中p62蛋白对脂质代谢相关的自噬以及炎症因子表达的影响,为p62在抗动脉粥样硬化中的应用提供参考。 方法 利用Ox-LDL刺激RAW264.7细胞的方法模拟巨噬源性泡沫细胞的形成,通过Western blot及实时荧光定量PCR检测巨噬源性泡沫细胞中p62蛋白和mRNA水平。通过Western blot比较p62 siRNA组和对照组中Ox-LDL诱导的LC3剪切、脂滴相关蛋白Plin2和过氧化物酶体相关蛋白PEX2的蛋白水平,通过实时荧光定量PCR比较TNFα和IL-6 mRNA表达水平。 结果 Ox-LDL对RAW264.7细胞中p62蛋白以及mRNA水平均有上调作用。干扰p62的表达之后,LC3-Ⅱ蛋白水平降低,Plin2的蛋白水平并无明显变化,PEX2的蛋白水平升高,TNFα和IL-6 mRNA表达升高。进一步研究发现,干扰Nrf2后能明显抑制Ox-LDL对p62的上调作用。 结论 巨噬源性泡沫细胞中Ox-LDL通过Nrf2介导p62蛋白的上调,p62可能具有抗动脉粥样硬化的作用。

English Abstract

林张军, 李倩, 章越凡, 芮耀诚. 巨噬源性泡沫细胞中p62蛋白上调作用和机制的研究[J]. 药学实践与服务, 2019, 37(5): 400-405,426. doi: 10.3969/j.issn.1006-0111.2019.05.004
引用本文: 林张军, 李倩, 章越凡, 芮耀诚. 巨噬源性泡沫细胞中p62蛋白上调作用和机制的研究[J]. 药学实践与服务, 2019, 37(5): 400-405,426. doi: 10.3969/j.issn.1006-0111.2019.05.004
LIN Zhangjun, LI Qian, ZHANG Yuefan, RUI Yaocheng. A study on the role and mechanism of upregulated p62 protein in macrophage-derived foam cells[J]. Journal of Pharmaceutical Practice and Service, 2019, 37(5): 400-405,426. doi: 10.3969/j.issn.1006-0111.2019.05.004
Citation: LIN Zhangjun, LI Qian, ZHANG Yuefan, RUI Yaocheng. A study on the role and mechanism of upregulated p62 protein in macrophage-derived foam cells[J]. Journal of Pharmaceutical Practice and Service, 2019, 37(5): 400-405,426. doi: 10.3969/j.issn.1006-0111.2019.05.004
参考文献 (32)

目录

    /

    返回文章
    返回