Lyczak Jeffrey B, Pier Gerald B
The Channing Laboratory, Brigham and Women's Hospital, and Harvard Medical School, Boston, Massachusetts 02115, USA.
Infect Immun. 2002 Nov;70(11):6416-23. doi: 10.1128/IAI.70.11.6416-6423.2002.
The cystic fibrosis transmembrane conductance regulator (CFTR) protein is an epithelial receptor mediating the translocation of Salmonella enterica serovar Typhi to the gastric submucosa. Since the level of cell surface CFTR is directly related to the efficiency of serovar Typhi translocation, the goal of this study was to measure CFTR expression by the intestinal epithelium during infection. CFTR protein initially present in the epithelial cell cytoplasm was rapidly trafficked to the plasma membrane following exposure to live serovar Typhi or bacterial extracts. CFTR-dependent bacterial uptake by epithelial cells increased (>100-fold) following CFTR redistribution. The bacterial factor which triggers CFTR redistribution is heat and protease sensitive. These data suggest that serovar Typhi induces intestinal epithelial cells to increase membrane CFTR levels, leading to enhanced bacterial ingestion and submucosal translocation. This could be a key, early step in the infectious process leading to typhoid fever.
囊性纤维化跨膜传导调节因子(CFTR)蛋白是一种上皮受体,介导肠炎沙门氏菌伤寒血清型向胃黏膜下层的转运。由于细胞表面CFTR的水平与伤寒血清型转运效率直接相关,本研究的目的是测量感染期间肠道上皮细胞中CFTR的表达。暴露于活的伤寒血清型或细菌提取物后,最初存在于上皮细胞质中的CFTR蛋白迅速转运至质膜。CFTR重新分布后,上皮细胞对CFTR依赖性细菌的摄取增加(>100倍)。触发CFTR重新分布的细菌因子对热和蛋白酶敏感。这些数据表明,伤寒血清型诱导肠道上皮细胞增加膜CFTR水平,导致细菌摄取和黏膜下转运增强。这可能是导致伤寒热的感染过程中的一个关键早期步骤。