Please wait a minute...

中国生物工程杂志

China Biotechnology
China Biotechnology  2011, Vol. 31 Issue (5): 22-27    DOI:
    
Effects of Hepatocellular Carcinoma Cells' Apoptosis and the Related Mechanisms after Indoleamine 2,3-Dioxygenase Gene Transfection
BU Xiao-qian, ZHANG Rui, SHENG Hui-qin, LUO Jing, LIU Yan, ZHANG Lu-ying, LIU Chun-liang, WANG Qi
Shanxi Medical University,Taiyuan 030001,China
Download: HTML   PDF(1172KB) HTML
Export: BibTeX | EndNote (RIS)      

Abstract  

Objective:To explore after indoleamine-2,3-dioxygenase(IDO)gene transfection the influence of the hepatocellular carcinoma cells’ apoptosis and the related cellular immune mechanisms by cell culture and in vivo. Methods: By cell culture and gene transfection technology,T-lymphocytes freshly isolated from healthy people and hepatocellular carcinoma cells were cocultured. The experiments were divided into six groups: T-lymphocytes and HepG2 cells group, T-lymphocytes and pcDNA3.1-HepG2 cells group, T-lymphocytes and pcDNA3.1-IDO-HepG2 cells group,and the three intervention groups which were added to IDO inhibitor 1-MT(1-methyl-tryptophan) on the basis of the above three groups. After two days of combine reaction, the apoptosisrate of HepG2 cell and the cytotoxicity of T-lymphocyte against HepG2 cell were examined by flow cytometer and MTT assay. After five days in mixed culture,the percentage of regulatory T cells(Treg) were analyzed by flow cytometer. Through establishment of the mouse model of human liver cancer cells, the percentage of Treg cells in peripheral blood of mouse was analyzed by flow cytometer. Results: 1.After two days of combine reaction, the apoptosis rate of HepG2 cell and the cytotoxicity of T-lymphocyte against HepG2 cell in IDO-HepG2 group were significantly lower than which in pcDNA3.1-HepG2 and HepG2 groups. They were respectively (1.65 ±0. 14) % and (35.00±2.20)% (p<0.05). With 1-MT groups, the above indexes were significantly higher than before the intervention (p<0.05). 2.After five days in mixed culture,the percentage of Treg cells in IDO-HepG2 group was significant higher and that was(10.53±1.05)%,it was considered statistically significant compared with the control group without 1-MT. In adding 1-MT groups, it decreased significantly (p<0.05). 3.In the mouse model of human liver cancer cells, the percentage of Treg cells in peripheral blood of IDO-HepG2 group increased significantly, that is (15.33 ±1.18)% and compared with the other two groups was statistically significant (p<0.05). Conclusion: 1.Though increasing the percentage of Treg cells in T-lymphocytes, IDO can suppress the apoptosis rate of hepatocellular carcinoma cells and the cytotoxicity of T-lymphocyte. 1-MT can reverse the role of IDO. 2.In vivo test, it can be confirmed that over-expression of IDO can increase the proportion of Treg cells in peripheral blood.



Key wordsIndoleamine 2      3-dioxygenase      Hepatocellular carcinoma cells      T-lymphocyte      Treg cells      Apoptosis     
Received: 28 December 2010      Published: 27 May 2011
ZTFLH:  Q813  
Cite this article:

BU Xiao-qian, ZHANG Rui, SHENG Hui-qin, LUO Jing, LIU Yan, ZHANG Lu-ying, LIU Chun-liang, WANG Qi. Effects of Hepatocellular Carcinoma Cells' Apoptosis and the Related Mechanisms after Indoleamine 2,3-Dioxygenase Gene Transfection. China Biotechnology, 2011, 31(5): 22-27.

URL:

https://manu60.magtech.com.cn/biotech/     OR     https://manu60.magtech.com.cn/biotech/Y2011/V31/I5/22


[1] Schrcksnadel K, Wirleitner B,Winkler C, et al. Monitoring tryptophan metabolism in chronic immune activation . Clin Chim Acta, 2006, 364(1-2):82-90.

[2] Munn D H,Mellor A L. Indoleamine 2,3-dioxygenase and tumor-induced tolerance.J Clin Invest,2007, 117(5):1147-1154.

[3] Lee S Y, Choi H K, Lee K J,et al. The immune tolerance of cancer is mediated by IDO that is inhibited by COX-2 inhibitors through regulatory T cells. J Immunother, 2009,32(1):22-28.

[4] Curti A, Pandolfi S, Valzasina B,et al. Modulation of tryptophan catabolism by human leukemic cells results in the conversion of CD25- into CD25+ T regulatory cells.Blood,2007,109(7):2871-2877.

[5] Babak B, Phillip R C, Madhav D S, et al. IDO Activates Regulatory T Cells and Blocks Their Conversion into Th17-Like T Cells. The Journal of Immunology, 2009, 183(4): 2475 -2483.

[6] Li M O, Flavell R A.TGF-β:a master of all T cell trades.Cell,2008,134(3):392-404.

[7] Korn T, Oukka M, Kuchroo V,et al.Th17 cells: effector T cells with inflammatory properties.Semin Immunol,2007,19(6):362-371.

[8] Rubtsov Y P, Rudensky A Y .TGF-β signalling in control of T-cell-mediated self-reactivity. Nat Rev Immunol,2007,7(6):443-453.

[9] Dong C. TH17 cells in development: an updated view of their molecular identity and genetic programming. Nat Rev Immunol,2008,8(5):337-348.

[10] Kim Y H, Choi B K, Kang W J, et al. IFN-γ-indoleamine-2,3 dioxygenase acts as a major suppressive factor in 4-1BB-mediated immune suppression in vivo. J Leukoc Biol,2009,85(5),817-825.

[1] TAO Shou-song,REN Guang-ming,YIN Rong-hua,YANG Xiao-ming,MA Wen-bing,GE Zhi-qiang. Knockdown of Deubiquitinase USP13 Inhibits the Proliferation of K562 Cells[J]. China Biotechnology, 2021, 41(5): 1-7.
[2] DUAN Yang-yang,ZHANG Feng-ting,CHENG Jiang,SHI Jin,YANG Juan,LI Hai-ning. The Effect of SIRT2 on Apoptosis and Mitochondrial Function in Parkinson’s Disease Model Cells Induced by MPP+[J]. China Biotechnology, 2021, 41(4): 1-8.
[3] ZHU Yongzhao,TAO Jin,REN Meng-meng,XIONG Ran,HE Ya-qin,ZHOU Yu,LU Zhen-hui,DU Yong,YANG Zhi-hong. Autophagy Protects Against Apoptosis of Human Placental Mesenchymal Stem Cells of Fetal Origin Induced by Tumor Necrosis Fator-α[J]. China Biotechnology, 2019, 39(9): 62-67.
[4] Ye LIU,Yue PAN,Wei ZHENG,Jing HU. miR-186-5p is Expressed Highly in Ethanol-induced Cardiomyocytes and Regulates Apoptosis by Target Gene XIAP[J]. China Biotechnology, 2019, 39(5): 53-62.
[5] Lu WANG,Li-yuan YANG,Yu-ting TANG,Yao TAO,Li LEI,Yi-pei JING,Xue-ke JIANG,Ling ZHANG. Effects of PKM2 Knockdown on Proliferation and Apoptosis of Human Leukemia Cells and Its Potential Mechanism[J]. China Biotechnology, 2019, 39(3): 13-20.
[6] Xiang HUANG,Jie YANG,Pei-yan HE,Zhi-hui WU,Hui-lan ZENG,Xin-Ning WANG,Jian-wei JIANG. Molecular Mechanism of Inducing 2774-C10 Cell Apoptosis and G1/S Cell Cycle Arrest by Ethanol Extract from Elephantopus mollis H.B.K.[J]. China Biotechnology, 2018, 38(4): 17-23.
[7] DAI Li-ting, WU Zhong-nan, HUANG Xiang, YANG Jie, ZENG Hui-lan, WANG Guo-cai, JIANG Jian-wei. Molecular Mechanism of Inducing GLC-82 Cells Apoptosis by Ethanol Extract from Wedelia prostrate(Hook.et Arn.) Hemsl[J]. China Biotechnology, 2017, 37(8): 1-7.
[8] XU An-jian, LI Yan-meng, LI Si-wen, WU Shan-na, ZHANG Bei, HUANG Jian. The Effect of PHP14 Knockdown on Lung Cancer Cells Apoptosis and Its Mechanism[J]. China Biotechnology, 2017, 37(7): 12-17.
[9] LI Yan-wei, MA Yi, HAN Lei, XIAO Xing, DANG Shi-ying, WEN Tao, WANG De-hua, FAN Zhi-yong. A Preliminary Study on Fas Apoptosis Inhibitory Molecule FAIM 1 Inducing and Simple Obesity[J]. China Biotechnology, 2017, 37(6): 37-42.
[10] BAI Xin-yan, WEN Li-min, WANG Yu-jing, WANG Hai-long, XIE Jun, GUO Rui. ANKRD49 Inhibits UV-induced Apoptosis of GC-1 Cells by Up-regulating Bcl-xL[J]. China Biotechnology, 2017, 37(4): 40-47.
[11] LI Zhen-hua, LI Cui-ping, ZHANG Xiang-qiang, DAI Li-ting, TANG Meng-si, WANG Guo-cai, JIANG Jian-wei, CAO Ming-rong. EM-3 Targets Stat3 to Induce Apoptosis, G2/M Cell Cycle Arrest and Reduce the Proportion of SP Cells in Nasopharyngeal Carcinoma[J]. China Biotechnology, 2016, 36(3): 1-10.
[12] WAN Chun-hong, ZHANG Zhi, LI Sheng-na, PENG Yi-yuan, XU Liang-guo. Research Progresses on TRAF7[J]. China Biotechnology, 2016, 36(3): 93-101.
[13] ZHANG Ying-min, ZHAO Na, LI Yong-fang, MENG Fan-xiu, ZHANG Qi, GAO Ran-peng, ZHANG Yue-hong, YU Bao-feng, GUO Rui, WANG Hai-long, XIE Jun, XU Jun. Targeted Treatment of Hepatoma Using HSV-TK Suicide Gene with The PBI-SUR-TK Vector[J]. China Biotechnology, 2016, 36(2): 16-21.
[14] CHEN Na-zi, JIANG Chao, LI Xiao-kun. Role of Endoplasmic Reticulum Stress in Diseases[J]. China Biotechnology, 2016, 36(1): 76-85.
[15] MENG Zan, XU Dan, LI Zhen, LI Jing, LI Gang, LIU Yong-gang, LIU Zhao yu, WU Hong, TANG Yong, PENG Yan. Oxygen Glucose Deprivation-induced Apoptosis in Oligodendrocytes Through TRPC3[J]. China Biotechnology, 2015, 35(4): 23-29.