Shu Xiaodong, Huang Jie, Dong Yuan, Choi Jayoung, Langenbacher Adam, Chen Jau-Nian
Department of Molecular, Cell and Developmental Biology, University of California, Los Angeles, CA 90095, USA.
Development. 2007 May;134(10):1921-30. doi: 10.1242/dev.02851. Epub 2007 Apr 18.
A conserved molecular cascade involving Nodal signaling that patterns the laterality of the lateral mesoderm in vertebrates has been extensively studied, but processes involved in the initial break of left-right (LR) symmetry are just beginning to be explored. Here we report that Na,K-ATPase alpha2 and Ncx4a function upstream of Nodal signaling to regulate LR patterning in zebrafish. Knocking down Na,K-ATPase alpha2 and Ncx4a activity in dorsal forerunner cells (DFCs), which are precursors of Kupffer's vesicle (KV), is sufficient to disrupt asymmetric gene expression in the lateral plate mesoderm and randomize the placement of internal organs, indicating that the activity of Na,K-ATPase alpha2 and Ncx4a in DFCs/KV is crucial for LR patterning. High-speed videomicroscopy and bead implantation experiments show that KV cilia are immobile and the directional fluid flow in KV is abolished in Na,K-ATPase alpha2 and Ncx4a morphants, suggesting their essential role in KV ciliary function. Furthermore, we found that intracellular Ca(2+) levels are elevated in Na,K-ATPase alpha2 and Ncx4a morphants and that the defects in ciliary motility, KV fluid flow and placement of internal organs induced by their knockdown could be suppressed by inhibiting the activity of Ca(2+)/calmodulin-dependent protein kinase II. Together, our data demonstrate that Na,K-ATPase alpha2 and Ncx4a regulate LR patterning by modulating intracellular calcium levels in KV and by influencing cilia function, revealing a previously unrecognized role for calcium signaling in LR patterning.
一个涉及Nodal信号传导的保守分子级联反应,它决定了脊椎动物侧中胚层的左右模式,已经得到了广泛研究,但左右(LR)对称性初始打破过程中涉及的机制才刚刚开始被探索。在这里,我们报告说,Na,K - ATP酶α2和Ncx4a在Nodal信号传导上游发挥作用,以调节斑马鱼的LR模式。敲低背侧先驱细胞(DFC)中的Na,K - ATP酶α2和Ncx4a活性,DFC是库普弗囊泡(KV)的前体,足以破坏侧板中胚层中的不对称基因表达,并使内部器官的位置随机化,这表明DFC / KV中Na,K - ATP酶α2和Ncx4a的活性对于LR模式形成至关重要。高速摄像显微镜和珠子植入实验表明,在Na,K - ATP酶α2和Ncx4a morphants中,KV纤毛不动,KV中的定向流体流动被消除,这表明它们在KV纤毛功能中起重要作用。此外,我们发现Na,K - ATP酶α2和Ncx4a morphants中的细胞内Ca(2+)水平升高,并且通过抑制Ca(2+)/钙调蛋白依赖性蛋白激酶II的活性,可以抑制由它们的敲低诱导的纤毛运动、KV流体流动和内部器官位置的缺陷。总之,我们的数据表明,Na,K - ATP酶α2和Ncx4a通过调节KV中的细胞内钙水平和影响纤毛功能来调节LR模式,揭示了钙信号在LR模式形成中以前未被认识的作用。