Porro Alessandro, Thiel Gerhard, Moroni Anna, Saponaro Andrea
Department of Biosciences, University of Milan, Milan, Italy.
Department of Biology, Technische Universität Darmstadt, Darmstadt, Germany.
Front Physiol. 2020 Jul 7;11:771. doi: 10.3389/fphys.2020.00771. eCollection 2020.
Direct regulation of the pacemaker "funny" current (I) by cyclic AMP (cAMP) underlies heart rate modulation by the autonomic nervous system. At the molecular level, cAMP activates hyperpolarization-activated cyclic nucleotide-gated (HCN) channels that drive I in sinoatrial node (SAN) myocytes. Even though HCN channel genes were identified more than 20 years ago, the understanding of how cAMP regulates their gating is still fragmented. Here we summarize present understanding on how the cAMP signal is transmitted from the cytosolic to the transmembrane (TM) domain in HCN4. We further discuss how detailed structural knowledge prompted the development of pharmacological/genetic tools for the control of cAMP regulation in these channels.
环磷酸腺苷(cAMP)对心脏起搏器“起搏”电流(I)的直接调节是自主神经系统调节心率的基础。在分子水平上,cAMP激活超极化激活的环核苷酸门控(HCN)通道,该通道驱动窦房结(SAN)心肌细胞中的I电流。尽管HCN通道基因在20多年前就已被鉴定出来,但对cAMP如何调节其门控的理解仍然支离破碎。在这里,我们总结了目前对cAMP信号如何从HCN4的胞质结构域传递到跨膜(TM)结构域的理解。我们还进一步讨论了详细的结构知识如何促使开发用于控制这些通道中cAMP调节的药理学/遗传学工具。