Erwert Ryan D, Eiting Kristine T, Tupper Joan C, Winn Robert K, Harlan John M, Bannerman Douglas D
Department of Medicine, University of Washington School of Medicine, Seattle, WA 98104, USA.
Microb Pathog. 2003 Aug;35(2):87-93. doi: 10.1016/s0882-4010(03)00100-1.
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.
志贺毒素(Stx)与多种人类和动物疾病状态的发病机制有关。Stx的一个关键宿主靶点是内皮细胞。Stx通过一种尚不清楚的机制诱导内皮细胞凋亡。在本报告中,我们证明Stx-1和Stx-2抑制抗凋亡Bcl-2家族成员Mcl-1在内皮细胞中的表达。Mcl-1表达的降低先于Stx诱导的凋亡发生。此外,Stx-1诱导的Mcl-1表达降低与对Stx-1诱导凋亡的敏感性呈剂量依赖性相关。最后,用蛋白酶体抑制剂乳胞素抑制Mcl-1降解可防止Stx-1诱导的凋亡。这些综合数据表明Mcl-1在保护内皮细胞免受Stx-1诱导的凋亡中发挥作用。