Henan Key Laboratory for Medical Tissue Regeneration, School of Basic Medical Sciences, Xinxiang Medical University, Xinxiang 453003, Henan Province, People's Republic of China.
Henan Collaborative Innovation Center of Molecular Diagnosis and Laboratory Medicine, School of Laboratory Medicine, Xinxiang Medical University, Xinxiang 453003, Henan Province, People's Republic of China.
Open Biol. 2021 Jun;11(6):210020. doi: 10.1098/rsob.210020. Epub 2021 Jun 2.
Smoothened is a key receptor of the hedgehog pathway, but the roles of Smoothened in cardiac development remain incompletely understood. In this study, we found that the conditional knockout of from the mesoderm impaired the development of the venous pole of the heart and resulted in hypoplasia of the atrium/inflow tract (IFT) and a low heart rate. The blockage of led to reduced expression of genes critical for sinoatrial node (SAN) development in the IFT. In a cardiac cell culture model, we identified a Gli2-Tbx5-Hcn4 pathway that controls SAN development. In the mutant embryos, the endocardial-to-mesenchymal transition (EndMT) in the atrioventricular cushion failed, and Bmp signalling was downregulated. The addition of Bmp2 rescued the EndMT in mutant explant cultures. Furthermore, we analysed scRNAseq and RNAseq data and explored the potential genes downstream of hedgehog signalling in posterior second heart field derivatives. In conclusion, our study reveals that Smoothened-mediated hedgehog signalling controls posterior cardiac progenitor commitment, which suggests that the mutation of might be involved in the aetiology of congenital heart diseases related to the cardiac conduction system and heart valves.
Smoothened 是 Hedgehog 通路的关键受体,但 Smoothened 在心脏发育中的作用仍不完全清楚。在这项研究中,我们发现条件敲除 会损害心脏静脉极的发育,导致心房/流入道(IFT)发育不良和心率降低。 阻断导致 IFT 中对窦房结(SAN)发育至关重要的基因表达减少。在心脏细胞培养模型中,我们确定了控制 SAN 发育的 Gli2-Tbx5-Hcn4 通路。在突变体胚胎中,房室瓣垫的心内膜向间质转化(EndMT)失败,Bmp 信号通路下调。添加 Bmp2 可挽救突变体外植体培养物中的 EndMT。此外,我们分析了 scRNAseq 和 RNAseq 数据,并探讨了 Hedgehog 信号下游在后二心脏场衍生物中的潜在基因。总之,我们的研究表明 Smoothened 介导的 Hedgehog 信号控制了心脏祖细胞的后向分化,这表明 突变可能与与心脏传导系统和心脏瓣膜相关的先天性心脏病的发病机制有关。