Pitcairn Emily, Harris Hannah, Epiney Justine, Pai Vaibhav P, Lemire Joan M, Ye Bin, Shi Nian-Qing, Levin Michael, McLaughlin Kelly A
Department of Biology and Allen Discovery Center at Tufts University, Medford, MA, USA.
Department of Medicine, University of Wisconsin-Madison, Madison, WI, USA.
Commun Integr Biol. 2017 May 10;10(3):e1309488. doi: 10.1080/19420889.2017.1309488. eCollection 2017.
Hyperpolarization-activated cyclic-nucleotide gated channel (HCN) proteins are important regulators of both neuronal and cardiac excitability. Among the 4 HCN isoforms, HCN4 is known as a pacemaker channel, because it helps control the periodicity of contractions in vertebrate hearts. Although the physiological role of HCN4 channel has been studied in adult mammalian hearts, an earlier role during embryogenesis has not been clearly established. Here, we probe the embryonic roles of HCN4 channels, providing the first characterization of the expression profile of any of the HCN isoforms during development and investigate the consequences of altering HCN4 function on embryonic pattern formation. We demonstrate that both overexpression of HCN4 and injection of dominant-negative HCN4 mRNA during early embryogenesis results in improper expression of key patterning genes and severely malformed hearts. Our results suggest that HCN4 serves to coordinate morphogenetic control factors that provide positional information during heart morphogenesis in .
超极化激活的环核苷酸门控通道(HCN)蛋白是神经元和心脏兴奋性的重要调节因子。在4种HCN亚型中,HCN4被认为是一种起搏通道,因为它有助于控制脊椎动物心脏收缩的周期性。尽管HCN4通道的生理作用已在成年哺乳动物心脏中得到研究,但其在胚胎发育早期的作用尚未明确确立。在此,我们探究HCN4通道的胚胎作用,首次对任何一种HCN亚型在发育过程中的表达谱进行表征,并研究改变HCN4功能对胚胎模式形成的影响。我们证明,在胚胎发育早期过表达HCN4和注射显性负性HCN4 mRNA均会导致关键模式基因表达异常以及心脏严重畸形。我们的结果表明,HCN4有助于协调形态发生控制因子,这些因子在心脏形态发生过程中提供位置信息。