畜牧兽医学报 ›› 2022, Vol. 53 ›› Issue (8): 2621-2632.doi: 10.11843/j.issn.0366-6964.2022.08.020

• 预防兽医 • 上一篇    下一篇

C5a/C5aR信号在微小隐孢子虫感染中的免疫调节作用研究

伍雪梅1, 杨新1, 原亚杰1, 尹艳玲1, 赖鹏1, 宋军科1, 史怀平2, 赵光辉1,3*   

  1. 1. 西北农林科技大学动物医学院, 杨凌 712100;
    2. 西北农林科技大学动物科技学院, 杨凌 712100;
    3. 中国农业科学院兰州兽医研究所, 兰州 730046
  • 收稿日期:2021-11-11 出版日期:2022-08-23 发布日期:2022-08-23
  • 通讯作者: 赵光辉,主要从事分子病原学和兽医免疫学研究,E-mail:zgh083@nwsuaf.edu.cn
  • 作者简介:伍雪梅(1995-),女,贵州施秉人,硕士生,主要从事隐孢子虫的致病性研究,E-mail:2019050504@nwafu.edu.cn;杨新(1987-),男,湖北应城人,讲师,博士,主要从事隐孢子虫的致病性研究,E-mail:xinyang@nwafu.edu.cn。伍雪梅和杨新为同等贡献作者
  • 基金资助:
    国家自然科学基金(31572509;32072890);家畜疫病病原生物学国家重点实验室开放基金(SKLVEB2020KFKT015);陕西省创新能力支撑计划项目(2021TD-31)

Immunomodulatory Effect of C5a/C5aR Signal during Cryptosporidium parvum Infection

WU Xuemei1, YANG Xin1, YUAN Yajie1, YIN Yanling1, LAI Peng1, SONG Junke1, SHI Huaiping2, ZHAO Guanghui1,3*   

  1. 1. College of Veterinary Medicine, Northwest A&F University, Yangling 712100, China;
    2. College of Animal Science and Technology, Northwest A&F University, Yangling 712100, China;
    3. Lanzhou Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Lanzhou 730046, China
  • Received:2021-11-11 Online:2022-08-23 Published:2022-08-23

摘要: 旨在探究C5a/C5aR信号在微小隐孢子虫感染过程中对宿主CD4+ T细胞免疫反应的调控作用。本研究以微小隐孢子虫(Cryptosporidium parvum)为研究对象,以BALB/c乳鼠和C5aR抑制BALB/c乳鼠为感染模型,应用实时荧光定量PCR和免疫组织化学技术检测了C.parvum感染前后乳鼠回肠组织中C5aR的表达变化,利用实时荧光定量PCR检测了隐孢子虫HSP70基因和CD4+ T细胞亚群(Th1、Th2、Th17细胞和Treg细胞)主效应细胞因子(IFN-γ、IL-4、IL-17和TGF-β)的转录变化,并通过病理组织切片观察乳鼠回肠黏膜的损伤情况。结果显示:与对照组乳鼠相比,C.parvum感染可以引起乳鼠回肠组织中C5aR的mRNA和蛋白表达水平显著上调(P<0.05),以及IFN-γ表达水平显著上调(P<0.05);与C.parvum感染组乳鼠相比,C5aR抑制剂处理可引起C.parvum感染乳鼠回肠组织中Th1细胞、Th2细胞和Treg细胞的主效应细胞因子IFN-γ、IL-4和TGF-β显著下调表达(P<0.05),以及Th17细胞主效应细胞因子IL-17显著上调表达(P<0.05)。病理学观察发现,抑制C5aR能显著改善C.parvum感染引起的乳鼠回肠组织的绒毛直径和黏膜厚度变化(P<0.05),但不能改善绒毛长度、绒毛长度与隐窝深度比值。隐孢子虫HSP70基因的mRNA水平检测发现,抑制C5aR能显著影响C.parvum在回肠组织中的增殖(P<0.05)。C5a/C5aR信号可能通过动态调节CD4+ T细胞亚群主效应细胞因子的表达来参与宿主与隐孢子虫相互作用的过程,为深入理解隐孢子虫与宿主的互作机制提供了参考。

关键词: 微小隐孢子虫, BALB/c乳鼠, C5a/C5aR信号, CD4+ T细胞亚群, 调节作用

Abstract: The aim of this study was to explore the regulation of C5a/C5aR signal in the immune response of host CD4+ T cell during Cryptosporidium parvum infection. We have utilized C. parvum as the research object, and selected BALB/c suckling mice and C5aR inhibited BALB/c suckling mice as infection models. The expression level of C5aR in the ileum tissues of BALB/c suckling mice was detected by using real-time PCR and immunohistochemistry. The expression patterns of C. parvum HSP70 gene and main effector cytokines (IFN-γ, IL-4, IL-17 and TGF-β) of CD4+ T cell subsets (Th1, Th2, Th17 cells and Treg cells) were analyzed by real-time PCR. The injury of ileal mucosa in suckling mice was observed by histopathology analysis. Compared with mice in the control group, C. parvum infection could significantly increase the expression levels of C5aR mRNA and protein (P<0.05), as well as IFN-γ in the ileum tissues of suckling mice (P<0.05). Compared with mice infected with C. parvum, the expression levels of main effector cytokines of Th1, Th2 and Treg cells, namely IFN-γ, IL-4 and TGF-β, significantly reduced in C5aR inhibited BALB/C suckling mice infected with C. parvum (P<0.05), and the expression level of IL-17, the main effector cytokine of Th17 cells, significantly increased in suckling mice treated with C5aR inhibitor (P<0.05). Histopathology analysis of ileal mucosa in suckling mice indicated inhibition of C5aR could significantly improve the changes of villus diameter and mucosal thickness of ileum caused by C. parvum infection (P<0.05), but not for the villus length and the ratio of villus length to crypt depth. Analysis of the mRNA level for Cryptosporidium HSP70 gene showed that inhibition of C5aR could significantly affect the proliferation of C. parvum in ileum (P<0.05). C5a/C5aR signal may participate in the process of interaction between host and Cryptosporidium by dynamically regulating the expression of major effector cytokines for CD4+ T cell subsets, providing reference basis for further understanding the interaction mechanism between Cryptosporidium spp. and host.

Key words: Cryptosporidium parvum, BALB/c sucking mouse, C5a/C5aR signal, CD4+ T cell subsets, regulation

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