Benham C D, Davis J B, Randall A D
Neurology Centre of Excellence for Drug Discovery, GlaxoSmithKline, New Frontiers Science Park, Harlow, UK.
Neuropharmacology. 2002 Jun;42(7):873-88. doi: 10.1016/s0028-3908(02)00047-3.
The emergence of the TRP (C) and vanilloid (TRPV) receptor family of Ca(2+) permeable channels has started to provide molecular focus to a linked group of ion channels whose common feature is activation primarily by intracellular ligands. These channels have a central role in Ca(2+) homeostasis in virtually all cells and in particular those that lack voltage-gated Ca(2+) channels. We will discuss recent work that is more precisely defining both molecular form and physiological function of this important group of Ca(2+) permeable channels with particular focus on the intracellular ligands that gate and modulate channel activity.
瞬时受体电位(C)和香草酸受体(TRPV)家族的钙离子通透通道的出现,开始为一组相关的离子通道提供了分子层面的关注焦点,这些通道的共同特征主要是由细胞内配体激活。这些通道在几乎所有细胞的钙离子稳态中都起着核心作用,尤其是那些缺乏电压门控钙离子通道的细胞。我们将讨论最近的研究工作,这些工作更精确地定义了这一重要的钙离子通透通道组的分子形式和生理功能,特别关注门控和调节通道活性的细胞内配体。