Alvarez de la Rosa D, Canessa C M, Fyfe G K, Zhang P
Department of Cellular and Molecular Physiology, Yale University School of Medicine, New Haven, Connecticut 06520-8026, USA.
Annu Rev Physiol. 2000;62:573-94. doi: 10.1146/annurev.physiol.62.1.573.
Amiloride-sensitive Na+ channels constitute a new class of proteins known as the ENaC-Deg family of ion channels. All members in this family share a common protein structure but differ in their ion selectivity, their affinity for the blocker amiloride, and in their gating mechanisms. These channels are expressed in many tissues of invertebrate and vertebrate organisms where they serve diverse functions varying from Na+ absorption across epithelia to being the receptors for neurotransmitters in the nervous system. Here, we review progress made during the last years in the characterization, regulation, and cloning of new amiloride-sensitive Na+ channels.
氨氯地平敏感的钠离子通道构成了一类新的蛋白质,即离子通道的ENaC-Deg家族。该家族的所有成员都具有共同的蛋白质结构,但在离子选择性、对阻滞剂氨氯地平的亲和力以及门控机制方面存在差异。这些通道在无脊椎动物和脊椎动物的许多组织中表达,发挥着多种功能,从上皮细胞对钠离子的吸收到神经系统中神经递质的受体。在此,我们综述了近年来在新型氨氯地平敏感钠离子通道的表征、调控和克隆方面取得的进展。