Blackwell J M
Department of Medicine, Addenbrooke's Hospital, Cambridge, UK.
Mol Med Today. 1996 May;2(5):205-11. doi: 10.1016/1357-4310(96)88773-9.
The ability of macrophages to become activated is central to antimicrobial immunity. Microbial stimuli can elicit a cascade of gene-inductive events mediating inflammation, elimination of the invading organism and induction of T-cell memory against reinvasion. Nramp1, a gene originally identified as Ity/Lsh/Bcg for its role in controlling Salmonella typhimurium, Leishmania donovani and Mycobacterium bovis infections in mice, regulates this cascade. Here we examine how the structure of the Nramp1 protein might relate to its function, and how variable expression of the human homologue (NRAMP1) might mediate enhanced resistance to infection but cause susceptibility to autoimmune disease.
巨噬细胞的激活能力是抗微生物免疫的核心。微生物刺激可引发一系列基因诱导事件,介导炎症反应、清除入侵生物体以及诱导针对再次入侵的T细胞记忆。Nramp1基因最初因其在控制小鼠鼠伤寒沙门氏菌、杜氏利什曼原虫和牛分枝杆菌感染中的作用而被鉴定为Ity/Lsh/Bcg,它调节这一过程。在这里,我们研究Nramp1蛋白的结构如何与其功能相关,以及人类同源物(NRAMP1)的可变表达如何介导对感染的增强抵抗力,但却导致对自身免疫性疾病的易感性。