Franco Diego, Sedmera David, Lozano-Velasco Estefanía
Cardiovascular Development Group, Department of Experimental Biology, University of Jaén, Jaén 23071, Spain.
Institute of Anatomy, Charles University, and Institute of Physiology, Czech Academy of Sciences, Prague 128 00, Czech Republic.
J Cardiovasc Dev Dis. 2017 Oct 11;4(4):16. doi: 10.3390/jcdd4040016.
Cardiac development is a complex morphogenetic process initiated as bilateral cardiogenic mesoderm is specified at both sides of the gastrulating embryo. Soon thereafter, these cardiogenic cells fuse at the embryonic midline configuring a symmetrical linear cardiac tube. Left/right bilateral asymmetry is first detected in the forming heart as the cardiac tube bends to the right, and subsequently, atrial and ventricular chambers develop. Molecular signals emanating from the node confer distinct left/right signalling pathways that ultimately lead to activation of the homeobox transcription factor Pitx2 in the left side of distinct embryonic organ anlagen, including the developing heart. Asymmetric expression of Pitx2 has therefore been reported during different cardiac developmental stages, and genetic deletion of Pitx2 provided evidence of key regulatory roles of this transcription factor during cardiogenesis and thus congenital heart diseases. More recently, impaired Pitx2 function has also been linked to arrhythmogenic processes, providing novel roles in the adult heart. In this manuscript, we provide a state-of-the-art review of the fundamental roles of Pitx2 during cardiogenesis, arrhythmogenesis and its contribution to congenital heart diseases.
心脏发育是一个复杂的形态发生过程,始于原肠胚形成期胚胎两侧特定的双侧生心中胚层。此后不久,这些生心细胞在胚胎中线融合,形成一个对称的线性心管。当心脏管向右弯曲时,在形成的心脏中首次检测到左右双侧不对称,随后心房和心室腔发育。来自节点的分子信号赋予不同的左右信号通路,最终导致同源盒转录因子Pitx2在不同胚胎器官原基的左侧被激活,包括发育中的心脏。因此,在不同的心脏发育阶段都报道了Pitx2的不对称表达,并且Pitx2的基因缺失为该转录因子在心脏发生过程以及先天性心脏病中的关键调节作用提供了证据。最近,Pitx2功能受损也与致心律失常过程有关,这表明其在成体心脏中具有新的作用。在本手稿中,我们对Pitx2在心脏发生、心律失常发生过程中的基本作用及其对先天性心脏病的贡献进行了最新综述。