Duess Johannes W, Fujiwara Naho, Corcionivoschi Nicolae, Puri Prem, Thompson Jennifer
National Children's Research Centre, Our Lady's Children's Hospital, Dublin, Ireland.
Pediatr Surg Int. 2013 Jan;29(1):13-8. doi: 10.1007/s00383-012-3202-7.
In chick embryos, administration of cadmium (Cd) induces ventral body wall defects (VBWD) similar to human omphalocele. It has been shown that failure of proper VBW formation may be due to disruption of somite development during early embryogenesis. In the VBWD chick model, Cd causes abnormal cell death in the somitic region resulting in improperly developed somites and tortuosity of the neural tube. However, the exact molecular mechanisms leading to VBWD still remain unclear. Wnt signaling is crucial during embryogenesis and plays a key role in normal somite formation. The Rho-associated coiled-coil containing protein kinase (ROCK) is involved in the non-canonical Wnt pathway which controls actin cytoskeleton assembly and cell contractility, and contributes to several developmental processes including somitogenesis. ROCK gene expression levels have recently been reported to be significantly decreased in the Cd-induced VBWD chick model. We designed this study to investigate the hypothesis that administration of ROCK inhibitor (Y-27632) in the absence of Cd disrupts somitogenesis and could contribute to the development of VBWD during early embryogenesis.
After 60 h of incubation chick embryos were transferred from eggs to culture dishes containing 20 μM of Y-27632 for experimental group (Y-27, n = 22) or chick saline for controls (n = 14). Following 24 h in the incubator they were assessed for stage development and gross abnormalities in morphology using the dissecting microscope. Western blot was performed to confirm Y-27632 inhibition of ROCK downstream signaling using an antibody against phosphorylated cofilin-2.
20 (90.9 %) embryos from Y-27 group and all controls were alive at examination. Morphological abnormalities were detected in 14 (70 %) Y-27 embryos. Somites appeared improperly developed, flattened in the cranio-caudal direction, and elongated in transverse direction in relation to controls. Chick embryos in Y-27 also presented with tortuosity of the neural tube in the lumbosacral region. Western blot analysis showed inhibition of cofilin-2 phosphorylation in affected embryos in comparison to controls.
Our study provides evidence that ROCK inhibitor results in the disruption of normal somitogenesis in chick embryos which may contribute to the failure of fusion of the anterior abdominal wall causing VBWD.
在鸡胚中,镉(Cd)的施用会诱发类似于人类脐膨出的腹侧体壁缺陷(VBWD)。研究表明,正常的腹侧体壁形成失败可能是由于胚胎早期发育过程中体节发育的破坏。在VBWD鸡模型中,镉会导致体节区域的异常细胞死亡,从而导致体节发育异常和神经管扭曲。然而,导致VBWD的确切分子机制仍不清楚。Wnt信号在胚胎发育过程中至关重要,在正常体节形成中起关键作用。含Rho相关卷曲螺旋的蛋白激酶(ROCK)参与非经典Wnt途径,该途径控制肌动蛋白细胞骨架组装和细胞收缩,并参与包括体节发生在内的多个发育过程。最近有报道称,在镉诱导的VBWD鸡模型中,ROCK基因表达水平显著降低。我们设计了本研究,以调查在无镉情况下施用ROCK抑制剂(Y-27632)会破坏体节发生并可能导致胚胎早期发育过程中VBWD发生这一假说。
孵化60小时后,将鸡胚从鸡蛋转移到含有20μM Y-27632的培养皿中作为实验组(Y-27,n = 22),或转移到含有鸡生理盐水的培养皿中作为对照组(n = 14)。在培养箱中放置24小时后,使用解剖显微镜评估它们的发育阶段和形态学上的大体异常。进行蛋白质免疫印迹法,使用抗磷酸化丝切蛋白-2抗体来确认Y-27632对ROCK下游信号的抑制作用。
Y-27组的20个(90.9%)胚胎和所有对照组胚胎在检查时均存活。在14个(70%)Y-27胚胎中检测到形态学异常。与对照组相比,体节发育异常,在头尾方向变扁平,在横向方向拉长。Y-27组的鸡胚在腰骶部区域也出现神经管扭曲。蛋白质免疫印迹分析显示,与对照组相比,受影响胚胎中的丝切蛋白-2磷酸化受到抑制。
我们的研究提供了证据,表明ROCK抑制剂会导致鸡胚正常体节发生受到破坏,这可能导致前腹壁融合失败,从而引起VBWD。