Institut für Experimentelle und Klinische Pharmakologie und Toxikologie der Albert-Ludwigs-Universität Freiburg, Albert-Str. 25, 79104 Freiburg, Germany.
Institut für Experimentelle und Klinische Pharmakologie und Toxikologie der Albert-Ludwigs-Universität Freiburg, Albert-Str. 25, 79104 Freiburg, Germany; Centre for Biological Signalling Studies (BIOSS), Germany.
Curr Opin Microbiol. 2015 Feb;23:55-61. doi: 10.1016/j.mib.2014.11.003. Epub 2014 Nov 22.
While bacterial effectors are often directly introduced into eukaryotic target cells by various types of injection machines, toxins enter the cytosol of host cells from endosomal compartments or after retrograde transport via Golgi from the ER. A first crucial step of toxin-host interaction is receptor binding. Using optimized protocols and new methods novel toxin receptors have been identified, including metalloprotease ADAM 10 for Staphylococcus aureus α-toxin, laminin receptor Lu/BCAM for Escherichia coli cytotoxic necrotizing factor CNF1, lipolysis stimulated lipoprotein receptor (LSR) for Clostridium difficile transferase CDT and low-density lipoprotein receptor-related protein (LRP) 1 for Clostridium perfringens TpeL toxin.
虽然细菌效应因子通常通过各种类型的注射机器直接引入真核靶细胞,但毒素是从内体区室或通过内质网逆行运输到高尔基体后进入宿主细胞的细胞质。毒素与宿主相互作用的第一步关键步骤是受体结合。使用优化的方案和新方法,已经鉴定出了新型毒素受体,包括金黄色葡萄球菌α-毒素的金属蛋白酶 ADAM10、大肠杆菌细胞毒性坏死因子 CNF1 的层粘连蛋白受体 Lu/BCAM、艰难梭菌转移酶 CDT 的脂肪分解刺激脂蛋白受体 (LSR) 和产气荚膜梭菌 TpeL 毒素的低密度脂蛋白受体相关蛋白 (LRP)1。