Mc Laughlin Danielle, Murphy Paula, Puri Prem
School of Natural Sciences, Trinity College Dublin, Dublin, Ireland.
National Children's Research Centre, Our Lady's Children's Hospital Crumlin, Dublin, Ireland.
Pediatr Surg Int. 2016 Jan;32(1):29-35. doi: 10.1007/s00383-015-3809-6. Epub 2015 Nov 7.
Tracheo-oesophageal malformations result from disturbed foregut separation during early development. The notochord, a specialised embryonic structure, forms immediately adjacent to the dividing foregut. In the Adriamycin mouse model of oesophageal atresia, foregut and notochord abnormalities co-exist, and the site and severity of foregut malformations closely correlate to the position and extent of the notochord defects. Notochord and foregut abnormalities also co-exist in the Noggin Knockout mouse as well in a small number of human cases. The notochord is a source of powerful molecular signals during early embryogenesis, being particularly important for neural crest development. The influence of notochord signaling on the adjacent foregut is not known. The purpose of this study was to examine the impact of notochord manipulation on foregut separation using a robust 3D explant method for culturing isolated foregut which permits oeosphageal and tracheal formation in vitro.
Foregut was micro-dissected from embryonic day 9 mice (License B100/4447 Irish Medicines Board), embedded in collagen and cultured for 48 h with native notochord intact (n = 6), notochord removed (n = 10) or additional notochord transplanted from stage matched controls (n = 8). Specimens were analysed for foregut morphology and molecular patterning using immunohistochemistry for Hnf3b (an endoderm marker) and Sox2 (a notochord and oesophageal marker) on cryosections.
Foregut separation into distinct oesophagus and trachea was observed in isolated foregut specimens with or without their native notochord. In specimens with additional notochord transplants, foregut morphology and molecular patterning were comparable to controls whether or not the native notochord was maintained. In particular foregut separation was not disrupted by the transplantation of additional notochord at the dorsal foregut endoderm.
The relationship between the embryonic foregut and notochord is complex and ill-defined; however, the notochord does not contribute essentially to oesophagus and trachea formation beyond E9 in the mouse, and the transplantation of additional notochord does not disrupt foregut separation in 3D explant culture.
气管食管畸形是由于早期发育过程中前肠分离紊乱所致。脊索是一种特殊的胚胎结构,紧邻正在分裂的前肠形成。在阿霉素诱导的食管闭锁小鼠模型中,前肠和脊索异常同时存在,前肠畸形的部位和严重程度与脊索缺陷的位置和范围密切相关。在Noggin基因敲除小鼠以及少数人类病例中,也存在脊索和前肠异常。脊索是早期胚胎发育过程中强大分子信号的来源,对神经嵴发育尤为重要。脊索信号对相邻前肠的影响尚不清楚。本研究的目的是使用一种强大的三维外植体方法培养分离的前肠,该方法允许在体外形成食管和气管,以研究脊索操作对前肠分离的影响。
从胚胎第9天的小鼠(爱尔兰药品管理局许可证B100/4447)中显微解剖前肠,包埋在胶原蛋白中,并在完整保留天然脊索(n = 6)、去除脊索(n = 10)或从阶段匹配的对照中移植额外脊索(n = 8)的情况下培养48小时。使用免疫组织化学方法对冷冻切片上的Hnf3b(一种内胚层标记物)和Sox2(一种脊索和食管标记物)进行分析,以观察前肠形态和分子模式。
在保留或去除天然脊索的分离前肠标本中,均观察到前肠分离为不同的食管和气管。在移植了额外脊索的标本中无论天然脊索是否保留,前肠形态和分子模式均与对照相当。特别是在前肠内胚层背侧移植额外脊索并不会破坏前肠分离。
胚胎前肠与脊索之间的关系复杂且不明确;然而,在小鼠中,脊索对胚胎第9天以后的食管和气管形成并无本质贡献,并且在三维外植体培养中移植额外脊索不会破坏前肠分离。