Uchida S
Second Department of Internal Medicine, Tokyo Medical and Dental University, School of Medicine, Japan.
Nihon Rinsho. 1996 Mar;54(3):667-71.
ClC chloride channels form a voltage-gated chloride channel family. It consists of at least 8 members of chloride channel, including the skeletal muscle-specific ClC-1 and the two very homologous kidney-specific chloride channels, ClC-K1 and ClC-K2. The dysfunction of ClC-1 is shown to lead to myotonia. Both ClC-K1 and ClC-K2 are involved in the transcellular chloride transport in the different nephron segments and may be involved in certain disorders of tubular function. This review focuses on (1) the structure and function of ClC chloride channels and (2) the involvement of ClC chloride channels in human diseases.
氯离子通道蛋白(ClC)氯离子通道构成了一个电压门控氯离子通道家族。它由至少8个氯离子通道成员组成,包括骨骼肌特异性的ClC-1以及两个高度同源的肾脏特异性氯离子通道ClC-K1和ClC-K2。研究表明,ClC-1功能异常会导致肌强直。ClC-K1和ClC-K2都参与不同肾单位节段的跨细胞氯离子转运,可能与某些肾小管功能障碍有关。本综述重点关注:(1)ClC氯离子通道的结构与功能;(2)ClC氯离子通道在人类疾病中的作用。