Limpitikul Worawan B, Dick Ivy E
Corrigan Minehan Heart Center, Massachusetts General Hospital, Boston, MA, USA.
Department of Physiology, University of Maryland School of Medicine, Baltimore, MD, USA.
J Gen Physiol. 2025 Mar 3;157(2). doi: 10.1085/jgp.202313531. Epub 2025 Jan 30.
Voltage-gated Ca2+ channels (VGCCs) are highly expressed throughout numerous biological systems and play critical roles in synaptic transmission, cardiac excitation, and muscle contraction. To perform these various functions, VGCCs are highly regulated. Inactivation comprises a critical mechanism controlling the entry of Ca2+ through these channels and constitutes an important means to regulate cellular excitability, shape action potentials, control intracellular Ca2+ levels, and contribute to long-term potentiation and depression. For CaV1 and CaV2 channel families, inactivation proceeds via two distinct processes. Voltage-dependent inactivation (VDI) reduces Ca2+ entry through the channel in response to sustained or repetitive depolarization, while Ca2+-dependent inactivation (CDI) occurs in response to elevations in intracellular Ca2+ levels. These processes are critical for physiological function and undergo exquisite fine-tuning through multiple mechanisms. Here, we review known determinants and modulatory features of these two critical forms of channel regulation and their role in normal physiology and pathophysiology.
电压门控钙通道(VGCCs)在众多生物系统中高度表达,在突触传递、心脏兴奋和肌肉收缩中发挥关键作用。为了执行这些各种功能,VGCCs受到高度调节。失活是控制Ca2+通过这些通道进入的关键机制,是调节细胞兴奋性、塑造动作电位、控制细胞内Ca2+水平以及促进长期增强和抑制的重要手段。对于CaV1和CaV2通道家族,失活通过两个不同的过程进行。电压依赖性失活(VDI)响应持续或重复去极化减少通过通道的Ca2+进入,而Ca2+依赖性失活(CDI)响应细胞内Ca2+水平升高而发生。这些过程对生理功能至关重要,并通过多种机制进行精细调节。在这里,我们综述了这两种关键通道调节形式的已知决定因素和调节特征及其在正常生理和病理生理中的作用。