CHINESE JOURNAL OF PARASITOLOGY AND PARASITIC DISEASES >
Effect of recombinant protein P29 on the TGF-β/Smad signaling pathway in the liver of mice infected with Echinococcus granulosus
Received date: 2018-09-25
Online published: 2019-07-10
Supported by
Supported by the Science and Technology Research of Ningxia (No. 2016KJHM42)
Objective To evaluate the effect of recombinant protein P29 (rP29), a 29 kDa antigen identified in hydatid cyst fluid which induces protective immunity, on the transforming growth factor-β (TGF-β)/Smad signaling pathway in the liver of mice infected with Echinococcus granulosus. Methods A group of 12 female BALB/c mice were subcutaneously immunized with 10 μg of rP29 emulsified with Freund’s adjuvant, then boosted twice with two weeks interval. Another two groups of mice were given with Freund’s adjuvant or PBS only as controls. The three groups of mice were intraperitoneally challenged with 1 500 protoscolex of E. granulosus per mouse two weeks after the last immunization. Twelve weeks after infection, the mice were euthanized and the liver tissues were collected. The TGF-β1 mRNA expression level was detected by RT-PCR in the liver of each infected mouse. The expression levels of TGF-β/Smad signaling pathway regulated downstream proteins such as TGF-RI, TGF-RII, p-Smad2,3, Smad4 and Smad7 were measured by Western blotting in the liver tissues. Results RT-PCR results showed that the relative expression level of TGF-β1 mRNA in the liver tissues of mice immunized with rP29 (1.24 ± 0.56) was reduced compared to PBS control mice (1.71 ± 0.29) with significant difference (P < 0.01), however, it was higher than that in adjuvant control mice (0.98 ± 0.42). The changes of the TGF-β1 mRNA expression level in the liver tissues were consistent with the TGF-β1 protein expression level detected by Western blotting. The expression density of TGF-β1 protein in the rP29 immunized group was 372.04 ± 0.01 (measured by densitometry) which was lower than that in the PBS group (673.02 ± 0.06), but higher than that in the adjuvant group (213.69 ± 0.31). The TGF-β/Smad signaling pathway-regulated downstream proteins also showed the similar changes except for Smad 7. The expression levels of TGF-β-RI, TGF-β-RII, p-Smad 2,3 and Smad 4 in the liver of rP29 immunized mice (357.59 ± 0.83, 289.07 ± 0.21, 204.06 ± 0.19, 396.11 ± 0.01, respectively) were reduced compared with the PBS group (496.89 ± 0.09, 378.41 ± 0.01, 428.11 ± 0.29, 566.95 ± 0.21, respectively), but higher than that of the adjuvant control group (171.99 ± 0.82, 185.77 ± 0.09, 128.09 ± 0.08, 205.87 ± 0.59, respectively). However, Smad 7 level expressed in rP29 immunized mice (278.89 ± 0.12) was up-regulated compared with PBS group (142.32 ± 0.07), but significantly lower than that in adjuvant group (384.17 ± 0.51). Conclusion Immunization of recombinant P29 protein significantly reduced the expression of TGF-β1 at both mRNA and protein levels in the liver of mice infected with E. granulosus. Most of the TGF-β/Smad signaling pathway-regulated downstream proteins (TGF-β-RI, TGF-β-RII, p-Smad 2,3 and Smad 4) were also reduced except for Smad 7 which was up-regulated.
Rui MA , Cheng LIU , Shi-mei XU , Ming-xing ZHU , Jia-qing ZHAO , Qiao-feng WAN , Jia-jia ZHU , Wei ZHAO . Effect of recombinant protein P29 on the TGF-β/Smad signaling pathway in the liver of mice infected with Echinococcus granulosus[J]. CHINESE JOURNAL OF PARASITOLOGY AND PARASITIC DISEASES, 2019 , 37(3) : 316 -321 . DOI: 10.12140/j.issn.1000-7423.2019.03.013
| [1] | 李润乐, 格日力. 我国包虫病基础研究现状及存在的问题[J]. 中国高原医学与生物学杂志, 2017, 38(4): 217-218, 234. |
| [2] | Cadavid Restrepo AM, Yang YR, McManus DP, et al. Environmental risk factors and changing spatial patterns of human seropositivity for Echinococcus spp. in Xiji County, Ningxia Hui Autonomous Region, China[J]. Parasit Vectors, 2018, 11(1): 159. |
| [3] | Kern P, Menezes da Silva A, Akhan O, et al. The echinococcoses: diagnosis, clinical management and burden of disease[J]. Adv Parasitol, 2017, 96: 259-369. |
| [4] | 张静宵,马霄, 刘玉芳, 等. 青海省棘球蚴病流行与分布情况调查[J]. 中国寄生虫学与寄生虫病杂志, 2017, 35(5): 465-467. |
| [5] | 宋健, 裴迎新, 郭卫东, 等. 2011-2017年内蒙古自治区棘球蚴病流行特征分析[J]. 中国寄生虫学与寄生虫病杂志, 2018, 36(6): 560-564. |
| [6] | 阿达来提·托留汉, 漫格库丽·哈提木拉提, 阿合里江·卡依多拉, 等. 新疆塔城地区棘球蚴病流行现状调查[J]. 中国寄生虫学与寄生虫病杂志, 2018, 36(6): 565-570. |
| [7] | 严信留, 贡桑曲珍, 伍卫平, 等. 西藏自治区村民和学生棘球蚴病知识态度和行为调查[J]. 中国寄生虫学与寄生虫病杂志, 2018, 36(1): 38-42. |
| [8] | 王东, 冯宇, 李凡, 等. 甘肃省藏区人群棘球蚴病流行现状调查及分析[J]. 中国寄生虫学与寄生虫病杂志, 2017, 35(2): 140-144. |
| [9] | 张梦媛, 伍卫平, 官亚宜, 等. 我国棘球蚴病疾病负担分析[J]. 中国寄生虫学与寄生虫病杂志, 2018, 36(1): 15-19, 25. |
| [10] | Cadavid Restrepo AM, Yang YR, McManus DP, et al. Spatiotemporal patterns and environmental drivers of human echinococcoses over a twenty-year period in Ningxia Hui Autonomous Region, China[J]. Parasit Vectors, 2018, 11(1): 108. |
| [11] | 何叶, 尹家祥. 棘球蚴病流行因素分析[J]. 中国热带医学, 2017, 17(4): 418-420. |
| [12] | 张文宝, 张壮志, 郑雪婷, 等. 棘球蚴(包虫)病预防疫苗的研制与应用[J]. 中国人兽共患病学报, 2018, 34(9): 834-838. |
| [13] | 师志云, 李昭宇, 卜阳, 等. 细粒棘球绦虫(中国大陆株)诊断抗原P-29基因的表达、纯化及免疫原性初步分析[J]. 中国人兽共患病学报, 2009, 25(11): 1065-1067. |
| [14] | Wang H, Li ZH, Gao F, et al. Immunoprotection of recombinant Eg.P29 against Echinococcus granulosus in sheep[J]. Vet Res Commun, 2016, 40(2): 73-79. |
| [15] | Zhao X, Zhang FB, Li ZW, et al. Bioinformatics analysis of EgA31. Bioinformatics analysis of EgA31 and EgG1Y162 proteins for designing a multi-epitope vaccine against Echinococcus granulosus[J]. Infect Genet Evol, 2019: S1567-S1348(19)30057-7. |
| [16] | Liu FX, Fan XX, Li L, et al. Development of recombinant goatpox virus expressing Echinococcus granulosus EG95 vaccine antigen[J]. J Virol Methods, 2018, 261: 28-33. |
| [17] | 张静, 曾静, 李亮, 等. Smad蛋白抑制剂SIS3对细粒棘球蚴原头节的作用研究[J]. 中国病原生物学杂志, 2017, 12(5): 389-393. |
| [18] | Hu HH, Chen DQ, Wang YN, et al. New insights into TGF-β/Smad signaling in tissue fibrosis[J]. Chem Biol Interact, 2018, 292(25): 76-83. |
| [19] | 张传山, 杨舒婷, 毕晓娟, 等. 泡型包虫病患者肝脏组织TGF-β1和Gadd45γ基因的表达及其在肝损伤中的作用研究[J]. 中国病原生物学杂志, 2016, 11(10): 908-912. |
| [20] | 陈骏, 钱云良. TGF-β/Smads通路与增生性瘢痕肌成纤维细胞分化[J]. 中国美容医学, 2007, 16(7): 1000-1003. |
| [21] | Yin S, Chen X, Zhang J, et al. The effect of Echinococcus granulosus on spleen cells and TGF-β expression in the peripheral blood of BALB/c mice[J]. Parasite Immunol, 2017, 39(3): e12415. |
| [22] | Pang NN, Zhang FB, Li SY, et al. TGF-β/Smad signaling pathway positively up-regulates the differentiation of Interleukin-9-producing CD4+ T cells in human Echinococcus granulosus infection[J]. J Infect, 2018, 76(4): 406-416. |
| [23] | Zhang CS, Wang LM, Wang H, et al. Identification and characterization of functional Smad8 and Smad4 homologues from Echinococcus granulosus[J]. Parasitol Res, 2014, 113(10): 3745-3757. |
| [24] | 单骄宇, 热比亚·努力, 李瑞, 等. 调节性T细胞转录因子Foxp3和IL-8在棘球蚴病患者肝组织病灶中的表达[J]. 中国寄生虫学与寄生虫病杂志, 2018, 36(3): 218-223. |
| [25] | Liu YM, Abudounnasier G, Zhang TC, et al. Increased expression of TGF-β1 in correlation with liver fibrosis during Echinococcus granulosus infection in mice[J]. Korean J Parasitol, 2016, 54(4): 519-525. |
| [26] | 印双红, 张俊波, 陈小林, 等. 细粒棘球蚴感染中阻断TGF-β1受体对淋巴细胞的影响[J]. 中国免疫学杂志, 2015, 31(5): 607-612. |
| [27] | 高富. 细粒棘球绦虫重组蛋白P29诱导绵羊的免疫保护力及其免疫机制研究[D]. 银川: 宁夏医科大学, 2015. |
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