Chau Mary D L, Tuft Richard, Fogarty Kevin, Bao Zheng-Zheng
Department of Medicine and Cell Biology, University of Massachusetts Medical School, Worcester, MA 01605, USA.
Mech Dev. 2006 Aug;123(8):626-40. doi: 10.1016/j.mod.2006.06.003. Epub 2006 Jul 14.
Results from lineage tracing studies indicate that precursor cells in the ventricles give rise to both cardiac muscle and conduction cells. Cardiac conduction cells are specialized cells responsible for orchestrating the rhythmic contractions of the heart. Here, we show that Notch signaling plays an important role in the differentiation of cardiac muscle and conduction cell lineages in the ventricles. Notch1 expression coincides with a conduction marker, HNK-1, at early stages. Misexpression of constitutively active Notch1 (NIC) in early heart tubes in chick exhibited multiple effects on cardiac cell differentiation. Cells expressing NIC had a significant decrease in expression of cardiac muscle markers, but an increase in expression of conduction cell markers, HNK-1, and SNAP-25. However, the expression of the conduction marker connexin 40 was inhibited. Loss-of-function study, using a dominant-negative form of Suppressor-of-Hairless, further supports that Notch1 signaling is important for the differentiation of these cardiac cell types. Functional studies show that the expression of constitutively active Notch1 resulted in abnormalities in ventricular conduction pathway patterns.
谱系追踪研究结果表明,心室中的前体细胞可分化为心肌细胞和传导细胞。心脏传导细胞是专门负责协调心脏有节奏收缩的细胞。在此,我们表明Notch信号通路在心室中心肌细胞和传导细胞谱系的分化中起重要作用。在早期阶段,Notch1的表达与一种传导标记物HNK-1一致。在鸡的早期心脏管中组成型激活的Notch1(NIC)的错误表达对心脏细胞分化产生了多种影响。表达NIC的细胞中,心肌标记物的表达显著降低,但传导细胞标记物HNK-1和SNAP-25的表达增加。然而,传导标记物连接蛋白40的表达受到抑制。使用显性负性形式的无毛抑制因子进行的功能丧失研究进一步支持Notch1信号通路对这些心脏细胞类型的分化很重要。功能研究表明,组成型激活的Notch1的表达导致心室传导通路模式异常。