期刊文献+

肠道共生菌在弓形虫感染过程中的作用研究进展

The Research Progress on the Role of Gut Commensal Bacteria Response to Toxoplasma gondii Infection
原文传递
导出
摘要 食入弓形虫卵囊和包囊是动物和人类感染弓形虫的主要途径,弓形虫进入小肠引发Th1细胞免疫反应和肠内稳态失调,诱导潘氏细胞呈IFN-γ依赖性缺失,出现共生菌菌群组成改变和细菌易位,引起肠道急性炎症反应,加剧弓形虫的感染和入侵。而无菌小鼠感染弓形虫后,肠道病理损伤轻微,且小鼠存活时间较长。此外,部分肠道共生菌在弓形虫感染过程中发挥分子佐剂的作用,和黏膜免疫共同维持免疫系统平衡防御病原入侵。可见,在弓形虫感染过程中,弓形虫感染进程、潘氏细胞缺失程度和肠道共生菌失调三者之间是相互促进的。该文就肠道共生菌与弓形虫感染的相关研究进行综述。 Ingestion of Toxoplasma gondii oocysts or cysts is the main pathway for infection of T.gondii in animals and humans.T.gondii enters the small intestine to initiate Th1 cellular immune response and intestinal dysbiosis,and induces Paneth cell loss,the changes of composition of commensal bacteria and translocation causing an acute inflammatory response in the intestine and increasing the infection and invasion of T.gondii.However,after germ-free mice infected with T.gondii,intestinal pathological damage is milder and the mice maintain a longer survival time.In addition,some gut commensal bacteria play a molecular adjuvant role in the infection of T.gondii.The commensal bacteria and mucosal immunity maintain the balance of immune system to defense against pathogen microbiota invasion.During the infection of T.gondii,the process of infection,the degree of Paneth cell loss and the process of gut commensal dysbacteria are mutually promoted.This paper reviews the related researchs on intestinal commensal bacteria and infection of T.gondii.
作者 苏瑞景 杨玉荣 SU Ruijing;YANG Yurong(Henan Agricultural University,College of Animal Science and Veterinary Medicine,Zhengzhou 450002)
出处 《中国细胞生物学学报》 CAS CSCD 2019年第10期1994-1999,共6页 Chinese Journal of Cell Biology
基金 中国博士后科学基金(批准号:2016M600577) 河南省高校科技创新人才支持计划(批准号:17HASTIT038) 河南省自然科学基金(批准号:162300410138)资助的课题~~
关键词 弓形虫 肠道共生菌 潘氏细胞 黏膜免疫 TH1 肠内稳态失调 Toxoplasma gondii gut commensal bacteria Paneth cell mucosal immunity Th1 gut commensal dysbacteria
  • 相关文献

参考文献3

二级参考文献54

  • 1高金岗,王士平,邢绥光.小白鼠十二指肠发育分化的组织学和组织化学观察[J].解剖学报,1995,26(4):425-430. 被引量:16
  • 2刘昀,陶凯忠,张顺民,康志敏,蒋春雷.人与鼠帕内特细胞分泌颗粒组织化学染色的比较[J].第二军医大学学报,2005,26(9):1074-1075. 被引量:1
  • 3Oppenheim J J, Yang D. Alarmins: chemotactic activators of immune responses. Curr Opin Immunol 2005; 17(4): 359-65.
  • 4Ganz T. Defensins: antimicrobial peptides of innate immunity. Nat Rev Immunol 2003; 3(9): 710-20.
  • 5Salzman NH, Underwood MA, Bevins CL. Paneth cells, defensins, and the commensal microbiota: A hypothesis on intimate interplay at the intestinal mucosa. Semin Immunol 2007; 19(2): 70-83.
  • 6Koslowski MJ, Beisner J, Stange EF, Wehkamp J. Innate an- timicrobial host defense in small intestinal Crohn's disease. Int J Med Microbiol 2010; 300(1): 34-40.
  • 7Bry L, Falk P, Huttner K, Ouellette A, Midtvedt T, Gordon JI. Paneth cell differentiation in the developing intestine of nor- mal and transgenic mice. Proc Natl Acad Sci USA 1994; 91: 10335-9.
  • 8Paterson JC, Watson SH. Paneth cell metaplasia in ulcerative colitis. Am J Pathol 1961; 38: 243-9.
  • 9Cunliffe RN, Rose FR, Keyte J, Abberley L, Chan WC, Mahida YR. Human defensin 5 is stored in precursor form in normal Paneth cells and is expressed by some villous epithelial cells and by metaplastic Paneth cells in the colon in inflammatory bowel disease. Gut 2001; 48: 176-85.
  • 10Nevalainen TJ, Gronroos JM, Kallajoki M. Expression of group Ⅱ phospholipase A2 in the human gastrointestinal tract. Lab Invest 1995; 72: 201-8.

共引文献13

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部