Shiga toxin induces decreased expression of the anti-apoptotic protein Mcl-1 concomitant with the onset of endothelial apoptosis

被引:30
作者
Erwerta, RD
Eiting, KT
Tupper, JC
Winn, RK
Harlan, JM
Bannerman, DD [1 ]
机构
[1] Univ Washington, Sch Med, Dept Med, Seattle, WA 98104 USA
[2] Univ Washington, Sch Med, Dept Surg, Seattle, WA 98104 USA
[3] ARS, Immunol & Dis Resistance Lab, USDA, ANRI, Beltsville, MD 20705 USA
关键词
Shiga-like toxin; endothelial; hemolytic uremic syndrome; apoptosis; Bcl-2;
D O I
10.1016/S0882-4010(03)00100-1
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Shiga toxin (Stx) has been implicated in the pathogenesis of several human and animal disease states. A key host target of Stx is the endothelial cell. Stx induces endothelial cell apoptosis through a mechanism that remains unknown. In the present report, we demonstrate that Stx-1 and Stx-2 inhibit endothelial cell expression of the anti-apoptotic Bcl-2 family member, Mcl-1. Decreased expression of Mcl-1 preceded the onset of Stx-induced apoptosis. Further, Stx-1-induced decrements in Mcl-1 expression correlated in a dose-dependent manner with sensitization to Stx-1-induced apoptosis. Finally, inhibition of Mcl-1 degradation with the proteasome inhibitor, lactacystin, protected against Stx-1-induced apoptosis. These combined data suggest a role for Mcl-1 in protecting endothelial cells against Stx-1-induced apoptosis. Published by Elsevier Ltd.
引用
收藏
页码:87 / 93
页数:7
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