Chen Y, Smith M R, Thirumalai K, Zychlinsky A
Skirball Institute, Department of Microbiology and Kaplan Cancer Center, New York University School of Medicine, 540 First Avenue, New York, NY 10016, USA.
EMBO J. 1996 Aug 1;15(15):3853-60.
Shigella, the etiological agent of dysentery, kills macrophages by inducing apoptosis. Deletion mutants in the invasion invasion plasmid antigen B (ipaB) of Shigella flexneri are not cytotoxic. Here, we localized IpaB to the cytoplasm of macrophages infected with S. flexneri. Purified IpaB induced apoptosis when microinjected into macrophages, indicating that IpaB is sufficient to induce apoptosis. Using a GST-IpaB fusion protein as a ligand in affinity purification, we isolated four IpaB binding proteins from macrophages which were identified as the precursor and the mature polypeptides of interleukin-1beta converting enzyme (ICE) or a highly homologous protease. We found that IpaB binds directly to ICE and this enzyme is activated during S. flexneri infection. Furthermore, specific inhibitors of ICE prevented Shigella-induced apoptosis.
痢疾杆菌是痢疾的病原体,它通过诱导细胞凋亡来杀死巨噬细胞。福氏志贺氏菌侵袭质粒抗原B(ipaB)的缺失突变体没有细胞毒性。在这里,我们将IpaB定位到感染福氏志贺氏菌的巨噬细胞的细胞质中。纯化的IpaB微注射到巨噬细胞中时可诱导细胞凋亡,这表明IpaB足以诱导细胞凋亡。使用GST-IpaB融合蛋白作为亲和纯化中的配体,我们从巨噬细胞中分离出四种IpaB结合蛋白,它们被鉴定为白细胞介素-1β转化酶(ICE)的前体和成熟多肽或一种高度同源的蛋白酶。我们发现IpaB直接与ICE结合,并且该酶在福氏志贺氏菌感染期间被激活。此外,ICE的特异性抑制剂可阻止志贺氏菌诱导的细胞凋亡。