Das Soumita, Jayaratne Rashini, Barrett Kim E
Department of Pathology, University of California San Diego School of Medicine, La Jolla, California.
Department of Medicine, University of California San Diego School of Medicine, La Jolla, California.
Cell Mol Gastroenterol Hepatol. 2018 Mar 5;6(1):33-45. doi: 10.1016/j.jcmgh.2018.02.009. eCollection 2018.
Every year, enteric infections and associated diarrhea kill millions of people. The situation is compounded by increases in the number of enteric pathogens that are acquiring resistance to antibiotics, as well as (hitherto) a relative paucity of information on host molecular targets that may contribute to diarrhea. Many forms of diarrheal disease depend on the dysregulation of intestinal ion transporters, and an associated imbalance between secretory and absorptive functions of the intestinal epithelium. A number of major transporters have been implicated in the pathogenesis of diarrheal diseases and thus an understanding of their expression, localization, and regulation after infection with various bacteria, viruses, and protozoa likely will prove critical in designing new therapies. This article surveys our understanding of transporters that are modulated by specific pathogens and the mechanism(s) involved, thereby illuminating targets that might be exploited for new therapeutic approaches.
每年,肠道感染及相关腹泻导致数百万人死亡。肠道病原体对抗生素产生耐药性的数量不断增加,以及(迄今为止)关于可能导致腹泻的宿主分子靶点的信息相对匮乏,使情况更加复杂。许多形式的腹泻病取决于肠道离子转运体的失调,以及肠道上皮细胞分泌和吸收功能之间的相关失衡。一些主要的转运体与腹泻病的发病机制有关,因此了解它们在感染各种细菌、病毒和原生动物后的表达、定位和调节,可能对设计新疗法至关重要。本文综述了我们对受特定病原体调节的转运体及其相关机制的理解,从而阐明了可能用于新治疗方法的靶点。