Zalk Ran, Lehnart Stephan E, Marks Andrew R
Department of Physiology and Cellular Biophysics, Columbia University College of Physicians and Surgeons, New York, New York 10032, USA.
Annu Rev Biochem. 2007;76:367-85. doi: 10.1146/annurev.biochem.76.053105.094237.
Ryanodine receptors (RyRs)/Ca2+ release channels, on the endoplasmic and sarcoplasmic reticulum of most cell types, are required for intracellular Ca2+ release involved in diverse cellular functions, including muscle contraction and neurotransmitter release. The large cytoplasmic domain of the RyR serves as a scaffold for proteins that bind to and modulate the channel's function and that comprise a macromolecular signaling complex. These proteins include calstabins [FK506-binding proteins (FKBPs)], calmodulin (CaM), phosphodiesterase, kinases, phosphatases, and their cognate targeting proteins. This review focuses on recent progress in the understanding of RyR regulation and disease mechanisms that are associated with channel dysfunction.
雷诺丁受体(RyRs)/钙离子释放通道存在于大多数细胞类型的内质网和肌浆网上,是细胞内钙离子释放所必需的,参与多种细胞功能,包括肌肉收缩和神经递质释放。RyR的大细胞质结构域作为蛋白质的支架,这些蛋白质与通道结合并调节其功能,构成一个大分子信号复合体。这些蛋白质包括钙稳定蛋白[FK506结合蛋白(FKBPs)]、钙调蛋白(CaM)、磷酸二酯酶、激酶、磷酸酶及其相关靶向蛋白。本综述重点关注对RyR调节以及与通道功能障碍相关的疾病机制的最新认识进展。