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表达人II型磷脂酶A2的转基因小鼠对大肠杆菌感染的抗性。

Resistance of transgenic mice expressing human group II phospholipase A2 to Escherichia coli infection.

作者信息

Laine V J, Grass D S, Nevalainen T J

机构信息

Department of Pathology, University of Turku, 20520 Turku, Finland.

出版信息

Infect Immun. 2000 Jan;68(1):87-92. doi: 10.1128/IAI.68.1.87-92.2000.

Abstract

Group II phospholipase A2 (PLA2) is a newly recognized antibacterial acute-phase protein. Recently we observed that transgenic mice expressing group II PLA2 (PLA2(+) mice) were able to resist experimental Staphylococcus aureus infection by killing the bacteria, as indicated by improved survival and by the small numbers of live bacteria in their tissues (V. J. O. Laine, D. S. Grass, and T. J. Nevalainen, J. Immunol. 162:7402-7408, 1999). To establish the role of group II PLA2 in Escherichia coli infection, the host responses of PLA2(+) mice and their PLA2-deficient C57BL/6J littermates (PLA2(-) mice) were studied after intraperitoneal administration of E. coli. The levels of group II PLA2 in sera of PLA2(+) mice increased after the administration of E. coli, and the concentration of group II PLA2 correlated significantly with the catalytic activity of PLA2 in serum. PLA2(+) mice showed lower rates of mortality and less bacterial growth in peritoneal lavage fluid, blood, and spleen and liver tissues than PLA2(-) mice. Unlike the observations with staphylococcal infection, serum and peritoneal lavage fluid did not inhibit the growth of E. coli in vitro. The results indicate that expression of the group II PLA2 transgene improves the host defense of mice against E. coli infection.

摘要

II 型磷脂酶 A2(PLA2)是一种新发现的具有抗菌作用的急性期蛋白。最近我们观察到,表达 II 型 PLA2 的转基因小鼠(PLA2(+)小鼠)能够通过杀死细菌来抵抗实验性金黄色葡萄球菌感染,这表现为生存率提高以及组织中存活细菌数量减少(V. J. O. Laine、D. S. Grass 和 T. J. Nevalainen,《免疫学杂志》162:7402 - 7408,1999 年)。为了确定 II 型 PLA2 在大肠杆菌感染中的作用,在腹腔注射大肠杆菌后,研究了 PLA2(+)小鼠及其 PLA2 缺陷的 C57BL/6J 同窝小鼠(PLA2(-)小鼠)的宿主反应。注射大肠杆菌后,PLA2(+)小鼠血清中 II 型 PLA2 的水平升高,且 II 型 PLA2 的浓度与血清中 PLA2 的催化活性显著相关。与 PLA2(-)小鼠相比,PLA2(+)小鼠在腹腔灌洗液、血液以及脾脏和肝脏组织中的死亡率更低,细菌生长也更少。与葡萄球菌感染的观察结果不同,血清和腹腔灌洗液在体外并不抑制大肠杆菌的生长。结果表明,II 型 PLA2 转基因的表达增强了小鼠对大肠杆菌感染的宿主防御能力。

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