Transgenic Mice With Elevated Level of CuZnSOD Are Highly Susceptible to Malaria Infection

详细信息	查看全文 | 推荐本文 |

• 作者：Golenser ; Jacob ; Peled-Kamar ; Mira ; Schwartz ; Eli ; Friedman ; Ilanit ; Groner ; Yoram ; Pollack ; Yaakov
• 关键词：Transgenic-CuZnSOD mice ; Malaria ; Oxidative stress ; Plasmodium ; Fenton’ ; s reaction ; Redox-active iron ; Free radical ; CuZnSOD ; copper zinc superoxide dismutase ; IFN ; interferon ; P. berghei ; Plasmodium berghei ; RBC ; red blood cells ; ROS ; reactive oxygen
• 刊名：Free Radical Biology and Medicine
• 出版年：1998
• 期刊代码：105_08915849
• 类别：med
• 出版时间：June, 1998
• 卷：24
• 期：9
• 页码：1504-1510
• 文件大小：100 K

摘要

Copper/zinc superoxide dismutase (CuZnSOD) catalyses the conversion of O₂^•− into H₂O₂. Constitutive overexpression of CuZnSOD in cells and animals creates an indigenous oxidative stress that predisposes them to added insults. In this study, we used transgenic CuZnSOD (Tg-CuZnSOD) mice with elevated levels of CuZnSOD to determine whether overexpression of CuZnSOD affected the susceptibility of these mice to plasmodium infection. Acute malaria is associated with oxidative stress, mediated by redox-active iron released from the infected RBC. Two independently derived Tg-CuZnSOD lines showed higher sensitivity than control mice to infection by Plasmodium berghei (P. berghei), reflected by an earlier onset and increased rate of mortality. Nevertheless, while Tg-CuZnSOD mice were more vulnerable than control mice, the levels of parasitemia were comparable in both strains. Moreover, treatment of infected red blood cells (RBC) with oxidative stress inducers, such as ascorbate or paraquat, reduced the viability of parasites equally in both transgenic and control RBC. This further confirms that increased CuZnSOD does not support plasmodia development. The data are consistent with the possibility that the combination of increased redox-active iron and elevated H₂O₂ in the plasmodium-infected Tg-CuZnSOD mice, led to an enhanced Fenton’s reaction-mediated HO^• production, and the resulting oxidative injury renders the transgenic mice more vulnerable to parasite infection.