中文English
ISSN 1001-5256 (Print)
ISSN 2097-3497 (Online)
CN 22-1108/R
Issue 8
Aug.  2016
Turn off MathJax
Article Contents

Hepatocyte autophagy model established by physical method

DOI: 10.3969/j.issn.1001-5256.2016.08.027
Research funding:

 

  • Received Date: 2016-02-19
  • Published Date: 2016-08-20
  • Objective To establish the autophagy model of normal human liver cell line 7702 induced by hypoxia and starvation,and to lay a foundation for further studies on the influence of autophagy on liver function. Methods The 7702 cells were selected and incubated with95% air and 5% CO2 at a temperature of 37 ℃( normal control group). The Binder three- gas incubator was used,with a temperature of37 ℃,a CO2 concentration of 5%,and an O2 concentration of 0. 3% to provide a hypoxic environment,and the serum- free DMEM was used to induce starvation. These cells were divided into 6-,12-,18-,and 24- hour hypoxia- starvation groups. Western blot was used to measure the protein expression of Beclin 1,Atg5,and LC3 in the normal control group and experimental groups,RT- q PCR was used to measure the mRNA expression of Beclin 1 and Atg5 in each group,and after transfection of LC3 plasmid,immunofluorescence assay was used to observe autophagy in each group. An analysis of variance was used for comparison of continuous data between groups,and the least significant difference t- test was used for further comparison between any two groups; the chi- square test was used for comparison of categorical data between groups. Results The 6- hour hypoxia- starvation groups had higher protein expression of Beclin 1,Atg5,and LC3 than the normal control group or other treated groups. Compared with all the other groups,the 6- hour hypoxia- starvation group showed significantly increased mRNA expression of Beclin 1 and Atg5,as well as significantly greater increases in the mRNA expression of Beclin 1and Atg5( all P < 0. 05). The hypoxia- starvation groups had significantly lower numbers of autophagosomes than the normal control group,and the 6- hour hypoxia- starvation group had the highest number of autophagosomes( all P < 0. 05). Conclusion Hypoxia and starvation established by physical methods can successfully induce hepatocyte autophagy,which is the most remarkable at 6 hours of hypoxia and starvation.

     

  • loading
  • [1]LIU YP,DONG L.Research advances in the role of autophagy in the development,progression,and treatment of liver cancer[J].Int J Dig Dis,2011,31(6):351-353.(in Chinese)刘亚萍,董蕾.自噬与肝癌发生发展和治疗的研究进展[J].国际消化病杂志,2011,31(6):351-353.
    [2]HUANG LW,XU LM.Relationship between liver diseases and autophagy[J].J Clin Hepatol,2014,30(2):186-188.(in Chinese)黄兰蔚,徐列明.细胞自噬在肝脏疾病中的作用[J].临床肝胆病杂志,2014,30(2):186-188.
    [3]GEBHARDT R,COFFER PJ.Hepatic autophagy is differentially regulated in periportal and pericentral zones-a general mechanism relevant for other tissues?[J].Cell Commun Signal,2013,11(1):21.
    [4]CHRISTIAN P,SACCO J,ADELI K.Autophagy:emerging roles in lipid homeostasis and metabolic control[J].Biochim Biophys Acta,2013,1831(4):819-824.
    [5]MA B,CAO W,LI W,et al.Dapper1 promotes autophagy by enhancing the Beclin1-Vps34-Atg14L complex formation[J].Cell Res,2014,24(8):912-924.
    [6]ZHANG DX,ZHANG JP,HU JY,et al.The potential regulatory roles of NAD+and its metabolism in autophagy[J].Metabolism,2016,65(4):456-462.
    [7]STEELE S,BRUNTON J,KAWULA T.The role of autophagy in intracellular pathogen nutrient acquisition[J].Front Cell Infect Microbiol,2015,5:51.
    [8]ROLANDO M,ESCOLL P,NORA T,et al.Legionella pneumophila S1P-lyase targets host sphingolipid metabolism and restrains autophagy[J].Proc Natl Acad Sci U S A,2016,113(7):1901-1906.
    [9]VAKIFAHMETOGLU-NORBERG H,XIA HG,YUAN J.Pharmacologic agents targeting autophagy[J].J Clin Invest,2015,125(1):5-13.
    [10]TANG Q,BU WH,WANG DD,et al.Advance research on interaction between autophagy and apoptosis and its influence in doevelopment of tumors[J].J Jilin Univ:Med Edit,2015,41(6):1303-1306.(in Chinese)唐琪,布文奂,王丹丹,等.自噬与凋亡的相互作用及其对肿瘤发展过程影响的研究进展[J].吉林大学学报:医学版,2015,41(6):1303-1306.
    [11]HARDAS SS,SULTANA R,WARRIER G,et al.Rat hippocampal responses up to 90 days after a single nanoceria dose extends a hierarchical oxidative stress model for nanoparticle toxicity[J].Nanotoxicology,2014,8(Suppl 1):155-166.
    [12]SONG W,SOO LEE S,SAVINI M,et al.Ceria nanoparticles stabilized by organic surface coatings activate the lysosome-autophagy system and enhance autophagic clearance[J].ACS Nano,2014,8(10):10328-10342.
    [13]HUANG J,BRUMELL JH.Bacteria-autophagy interplay:a battle for survival[J].Nat Rev Microbiol,2014,12(2):101-114.
    [14]ESCOLL P,ROLANDO M,BUCHRIESER C.Modulation of host autophagy during bacterial infection:sabotaging host munitions for pathogen nutrition[J].Front Immunol,2016,7:81.
    [15]FU ZY.Molecular mechanism and regulating factors of autophagy[J].J Clin Exp Med,2015,14(17):1488-1489.(in Chinese)付智勇.自噬的分子机制及其调控因素[J].临床和实验医学杂志,2015,14(17):1488-1489.
    [16]NOVAK I,KIRKIN V,McE WAN DG,et al.Nix is a selective autophagy receptor for mitochondrial clearance[J].EMBO Rep,2010,11(1):45-51.
    [17]RUBINSZTEIN DC,MARIO G,KROEMER G.Autophagy and aging[J].Cell,2011,146(5):682-695.
    [18]LIN CF,KUO YT,CHEN TY,et al.Quercetin-rich guava(psidium guajava)juice in combination with trehalose reduces autophagy,apoptosis and pyroptosis formation in the kidney and pancreas of type II diabetic rats[J].Molecules,2016,21(3):e334.
    [19]FRANOIS A,JULIAN A,RAGOT S,et al.Correction:inflammatory stress on autophagy in peripheral blood mononuclear cells from patients with alzheimer's disease during 24 months of followup[J].PLoS One,2016,11(3):e0143933.
    [20]CHUN SK,GO K,YANG MJ,et al.Autophagy in ischemic livers:a critical role of sirtuin 1/mitofusin 2 axis in autophagy induction[J].Toxicol Res,2016,32(1):35-46.
    [21]PROSKE J,WALTER L,BUMES E,et al.Adaptive immune response to and survival effect of temozolomide-and valproic acidinduced autophagy in glioblastoma[J].Anticancer Res,2016,36(3):899-905.
    [22]WANG KF,ZHU YK,MENG QH.Research advances in oxidative stress and mitochondrial permeability transition in liver failure[J].JClin Hepatol,2013,29(9):711-714.(in Chinese)王克菲,朱跃科,孟庆华.氧化应激、线粒体通透性转换与肝衰竭的相关性[J].临床肝胆病杂志,2013,2(9):711-714.
  • 加载中

Catalog

    通讯作者: 陈斌, bchen63@163.com
    • 1. 

      沈阳化工大学材料科学与工程学院 沈阳 110142

    1. 本站搜索
    2. 百度学术搜索
    3. 万方数据库搜索
    4. CNKI搜索

    Article Metrics

    Article views (2341) PDF downloads(502) Cited by()
    Proportional views
    Related

    /

    DownLoad:  Full-Size Img  PowerPoint
    Return
    Return