论著

细粒棘球蚴感染小鼠肝精氨酸酶的表达和功能研究

  • 曹胜魁 ,
  • 张小凡 ,
  • 魏玉环 ,
  • 潘佳明 ,
  • 曹建平 ,
  • 沈玉娟 ,
  • 陈家旭
展开
  • 中国疾病预防控制中心寄生虫病预防控制所,国家热带病研究中心,世界卫生组织热带病合作中心,科技部国家级热带病国际联合研究中心,卫生部寄生虫病原与媒介生物学重点实验室,上海 200025
曹胜魁(1988-),男,博士研究生,助理研究员,从事寄生虫病研究。E-mail: caosk@nipd.chinacdc.cn

收稿日期: 2019-11-21

  网络出版日期: 2020-07-07

基金资助

国家自然科学基金(81772224);国家科技重大专项(2018ZX10713001-004);上海市卫生和计划生育委员会青年基金(20164Y0085)

Expression and function of arginase in livers of mice infected with Echinococcus granulosus

  • Sheng-kui CAO ,
  • Xiao-fan ZHANG ,
  • Yu-huan WEI ,
  • Jia-ming PAN ,
  • Jian-ping CAO ,
  • Yu-juan SHEN ,
  • Jia-xu CHEN
Expand
  • WHO Collaborating Centre for Tropical Diseases;National Center for International Research on Tropical Diseases, Ministry of Science and Technology;Key Laboratory of Parasite and Vector Biology, Ministry of Health, Shanghai 200025, China

Received date: 2019-11-21

  Online published: 2020-07-07

Supported by

Supported by the National Natural Science Foundation of China(81772224);National Science and Technology Major Program of China(2018ZX10713001-004);Shanghai Municipal Commission of Health and Family Planning(20164Y0085)

摘要

目的 分析精氨酸酶(ARG)在细粒棘球蚴感染小鼠肝白细胞中的表达和功能。 方法 将18只雌性BALB/c小鼠随机分为感染组和对照组,每组9只。感染组小鼠腹腔注射细粒棘球蚴原头节2 000个/鼠,对照组注射等量生理盐水。感染后270 d,分离小鼠肝组织中白细胞。蛋白质印迹(Western blotting)分析肝白细胞中ARG和一氧化氮合酶(NOS)的表达情况,采用Image J软件分析蛋白质表达丰度。ARG活性检测试剂盒、尿素检测试剂盒和一氧化氮(NO)检测试剂盒检测肝中白细胞的ARG活性、肝组织的尿素和NO含量。流式细胞术分析肝多种髓系细胞中ARG-1和T细胞中CD3ζ的表达情况。采用SPSS 20.0统计学软件进行数据分析。 结果 Western blotting检测结果显示,感染组小鼠肝白细胞中ARG-1表达的灰度值为1.03 ± 0.01,高于对照组的0.12 ± 0.01(P < 0.01);感染组小鼠肝白细胞中ARG-2和诱导型一氧化氮合酶(iNOS)表达的灰度值分别为0.54 ± 0.01和0.64 ± 0.02,对照组分别为0.55 ± 0.02和0.59 ± 0.02,差异均无统计学意义(P > 0.05)。感染组小鼠肝白细胞中的ARG活性、肝组织中的尿素和NO含量分别为(0.03 ± 0.00)U/ml、(0.66 ± 0.02)mmol/L和(14.63 ± 1.55)μmol/L,对照组分别为(0.02 ± 0.00)U/ml、(0.04 ± 0.01)mmol/L和(29.22 ± 0.36)μmol/L,两组差异均有统计学意义(P < 0.05)。流式细胞术分析发现,ARG-1在感染组小鼠肝白细胞中CD11b+CD11c+、CD11b+F4/80+、CD11b+Gr-1+、CD11b+Gr-1+Ly-6C-Ly-6G+、CD11b+Gr-1+Ly-6C+-Ly-6G-和CD11b+Ly-6G+中表达的相对平均荧光密度分别为1.41 ± 0.12、1.21 ± 0.06、1.52 ± 0.16、1.30 ± 0.03、1.58 ± 0.12和1.21 ± 0.04,均高于对照组的1.00 ± 0.14、1.00 ± 0.05、1.00 ± 0.01、1.00 ± 0.07、1.00 ± 0.03和1.00 ± 0.02(P < 0.05)。CD3ζ在感染组小鼠肝CD4+和CD8+ T细胞中表达的相对平均荧光密度分别为0.82 ± 0.04和0.78 ± 0.05,均低于对照组的1.00 ± 0.05和1.00 ± 0.07(P < 0.05)。 结论 细粒棘球蚴感染小鼠肝白细胞中ARG-1表达增多,一定程度上拮抗NOS;肝CD4+和CD8+ T细胞中CD3ζ表达下调。

本文引用格式

曹胜魁 , 张小凡 , 魏玉环 , 潘佳明 , 曹建平 , 沈玉娟 , 陈家旭 . 细粒棘球蚴感染小鼠肝精氨酸酶的表达和功能研究[J]. 中国寄生虫学与寄生虫病杂志, 2020 , 38(3) : 304 -309 . DOI: 10.12140/j.issn.1000-7423.2020.03.008

Abstract

Objective To investigate the expression and function of arginase (ARG) in livers of mice infected with Echinococcus granulosus. Methods Eighteen female BALB/c mice were randomly divided into the infection and control group, 9 mice each. Mice in the infection group were each given 2 000 live protoscoleces of E. granulosus by intraperitoneal injection, while the control group was injected with the same volume of saline. Liver leukocytes were isolated 270 days after infection. The expression levels of ARG and nitric oxide synthase (NOS) were examined by Western blotting, and the protein abundance was analyzed with the Image J software. The ARG activity in liver leukocytes, and urea and nitric oxide contents in liver tissues were assessed with the ARG activity detection kit, urea detection kit and nitric oxide (NO) detection kit, respectively. The expression of ARG-1 in various myeloid cells and CD3ζ in T cells in the liver were analyzed by flow cytometry. Data were analyzed using the SPSS 20.0 software. Results Western blotting showed that the gray value of ARG-1 expression in liver leukocytes in the infection group was 1.03 ± 0.01, which was significantly higher than that in the control group (0.12 ± 0.01, P < 0.01); the expression gray value of ARG-2 and inducible nitric oxide synthase(iNOS) in the infection group was 0.54 ± 0.01 and 0.64 ± 0.02, while that of control group was 0.55 ± 0.02 and 0.59 ± 0.02, respectively; no significant differences were found between the groups (P > 0.05). In the infection group, the ARG activity in liver leukocytes, and urea and NO contents in liver tissues was (0.03 ± 0.00) U/ml, (0.66 ± 0.02) mmol/L and (14.63 ± 1.55) μmol/L, respectively, being significantly different from those in the control group [(0.02 ± 0.00) U/L, (0.04 ± 0.01) mmol/L, and (29.22 ± 0.36) μmol/L, respectively] (P < 0.05). Flow cytometry showed that the relative fluorescence density of ARG-1 expression in CD11b+CD11c+, CD11b+F4/80+, CD11b+Gr-1+, CD11b+Gr-1+Ly-6C-Ly-6G+, CD11b+Gr-1+Ly-6C+-Ly-6G- and CD11b+Ly-6G+ liver cells in the infection group were 1.41 ± 0.12, 1.21 ± 0.06, 1.52 ± 0.16, 1.30 ± 0.03, 1.58 ± 0.12 and 1.21 ± 0.04, respectively, all items being significantly higher than those in the control group (1.00 ± 0.14, 1.00 ± 0.05, 1.00 ± 0.01, 1.00 ± 0.07, 1.00 ± 0.03 and 1.00 ± 0.02; P < 0.05). The relative mean fluorescence density of CD3ζ in liver CD4+ and CD8+ T cells in the infection group were 0.82 ± 0.04 and 0.78 ± 0.05, respectively, both significantly lower than those in the control group (1.00 ± 0.05, 1.00 ± 0.07; P < 0.05). Conclusion Higher expression of ARG-1 in liver leukocytes was found in mice infected with E. granulosus, which may antagonize the NOS to some extent; meanwhile, the expression of CD3ζ in the CD4+ and the CD8+ T cells was down-regulated.

参考文献

[1] Budke CM, Carabin H, Ndimubanzi PC, et al. A systematic review of the literature on cystic echinococcosis frequency worldwide and its associated clinical manifestations[J]. Am J Trop Med Hyg, 2013,88(6):1011-1027.
[2] Wu WP, Wang H, Wang Q, et al. A nationwide sampling survey on echinococcosis in China during 2012-2016[J]. Chin J Parasitol Parasit Dis, 2018,36(1):1-14. (in Chinese)
[2] ( 伍卫平, 王虎, 王谦, 等. 2012-2016年中国棘球蚴病抽样调查分析[J]. 中国寄生虫学与寄生虫病杂志, 2018,36(1):1-14.)
[3] Vuitton DA. Echinococcosis and allergy[J]. Clinic Rev Allerg Immunol, 2004,26(2):93-104.
[4] Zheng YD. Strategies of Echinococcus species responses to immune attacks: implications for therapeutic tool development[J]. Int Immunopharmacol, 2013,17(3):495-501.
[5] Grubor NM, Jovanova-Nesic KD, Shoenfeld Y. Liver cystic echinococcosis and human host immune and autoimmune follow-up: a review[J]. World J Hepatol, 2017,9(30):1176-1189.
[6] Caldwell RW, Rodriguez PC, Toque HA, et al. Arginase: amultifaceted enzyme important in health and disease[J]. Physiol Rev, 2018,98(2):641-665.
[7] Alderton WK, Cooper CE, Knowles RG. Nitric oxide synthases: structure, function and inhibition[J]. Biochem J, 2001,357(3):593-615.
[8] Amri M, Touil-Boukoffa C. A protective effect of the laminated layer on Echinococcus granulosus survival dependent on upregulation of host arginase[J]. Acta Trop, 2015,149:186-194.
[9] Zea AH, Rodriguez PC, Culotta KS, et al. L-arginine modulates CD3ζ expression and T cell function in activated human T lymphocytes[J]. Cell Immunol, 2004,232(1/2):21-31.
[10] Xiao N, Qiu JM, Nakao M, et al. Short report: identification of Echinococcus species from a yak in the Qinghai-Tibet plateau region of China[J]. Am J Trop Med Hyg, 2003,69(4):445-446.
[11] Gong WC, Huang FJ, Sun L, et al. Toll-like receptor-2 regulates macrophage polarization induced by excretory-secretory antigens from Schistosoma japonicum eggs and promotes liver pathology in murine schistosomiasis[J]. PLoS Negl Trop Dis, 2018,12(12):e0007000.
[12] Díaz A, Casaravilla C, Allen JE, et al. Understanding the laminated layer of larval Echinococcus Ⅱ: immunology[J]. Trends Parasitol, 2011,27(6):264-273.
[13] Paredes R, Godoy P, Rodríguez B, et al. Bovine (Bos taurus) humoral immune response against Echinococcus granulosus and hydatid cyst infertility[J]. J Cell Biochem, 2011,112(1):189-199.
[14] El Kasmi KC, Qualls JE, Pesce JT, et al. Toll-like receptor-induced arginase 1 in macrophages thwarts effective immunity against intracellular pathogens[J]. Nat Immunol, 2008,9(12):1399-1406.
[15] Rodriguez PC, Quiceno DG, Zabaleta J, et al. Arginase Ⅰ production in the tumor microenvironment by mature myeloid cells inhibits T-cell receptor expression and antigen-specific T-cell responses[J]. Cancer Res, 2004,64(16):5839-5849.
[16] Bowcutt R, Bell LV, Little M, et al. Arginase-1-expressing macrophages are dispensable for resistance to infection with the gastrointestinal helminth Trichuris muris[J]. Parasite Immunol, 2011,33(7):411-420.
[17] Paduch K, Debus A, Rai B, et al. Resolution of cutaneous leishmaniasis and persistence of Leishmania major in the absence of arginase 1[J]. J Immunol, 2019,202(5):1453-1464.
[18] Cao SK, Pan W, Liu H, et al. Expression and activity of arginase from monocytic-type myeloid-derived suppressor cells in rats infected with Echinococcus granulosus[J]. Chin J Parasitol Parasit Dis, 2016,34(1):27-31. (in Chinese)
[18] ( 曹胜魁, 潘伟, 刘华, 等. 细粒棘球蚴感染小鼠单核髓源抑制性细胞精氨酸酶的表达和活性研究[J]. 中国寄生虫学与寄生虫病杂志, 2016,34(1):27-31.)
[19] Peng SS, Yu T, Wang L, et al. Influence of type 2 macrophages (M2) in echinococcosis[J]. Int J Clin Exp Pathol, 2016,9(3):4110-4116.
[20] Munder M, Eichmann K, Morán JM, et al. Th1/Th2-regulated expression of arginase isoforms in murine macrophages and dendritic cells[J]. J Immunol, 1999,163(7):3771-3777.
[21] Oberlies J, Watzl C, Giese T, et al. Regulation of NK cell function by human granulocyte arginase[J]. J Immunol, 2009,182(9):5259-5267.
[22] Bronte V, Serafini P, Mazzoni A, et al. L-arginine metabolism in myeloid cells controls T-lymphocyte functions[J]. Trends Immunol, 2003,24(6):301-305.
文章导航

/

〈 〉