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先天性巨结肠症中NEDL2表达降低。

Decreased expression of NEDL2 in Hirschsprung's disease.

作者信息

O'Donnell Anne Marie, Coyle David, Puri Prem

机构信息

National Children's Research Centre, Our Lady's Children's Hospital Crumlin, Dublin, Ireland.

National Children's Research Centre, Our Lady's Children's Hospital Crumlin, Dublin, Ireland.

出版信息

J Pediatr Surg. 2016 Nov;51(11):1839-1842. doi: 10.1016/j.jpedsurg.2016.06.016. Epub 2016 Jul 5.

Abstract

PURPOSE

NEDD4-like ubiquitin protein ligase 2 (NEDL2) plays an important role in many physiological and pathological processes. NEDL2 is a positive regulator of GDNF/Ret signaling during enteric neurogenesis. Mice lacking NEDL2 exhibit decreased numbers of enteric neurons, progressive bowel dysmotility and intestinal hypoganglionosis. We designed this study to investigate the expression of NEDL2 in the normal human colon and in HSCR.

METHODS

HSCR tissue specimens (n=10) were collected at the time of pull-through surgery and divided into aganglionic and ganglionic segments. Colonic control samples (n=10) were obtained from patients with imperforate anus at the time of colostomy closure. Immunolabeling of NEDL2 was visualized using confocal microscopy to assess protein distribution, while Western blot analysis was undertaken to quantify NEDL2 protein expression.

RESULTS

Confocal microscopy revealed that NEDL2-immunoreactivity colocalized with ICCs and neurons within the submucosa, myenteric plexus and smooth muscle in controls and ganglionic specimens, with markedly reduced NEDL2-immunoreactivity in aganglionic specimens. Western blotting revealed high levels of the NEDL2 protein in normal controls and the ganglionic region of HSCR, while there was a marked decrease in NEDL2 protein expression in the aganglionic region of HSCR.

CONCLUSION

We report, for the first time, the expression of NEDL2 in the human colon. The decreased expression of NEDL2 in the aganglionic colon suggests that NEDL2 may play a role in the pathophysiology of HSCR.

摘要

目的

NEDD4样泛素蛋白连接酶2(NEDL2)在许多生理和病理过程中发挥重要作用。在肠道神经发生过程中,NEDL2是胶质细胞源性神经营养因子(GDNF)/Ret信号通路的正向调节因子。缺乏NEDL2的小鼠肠道神经元数量减少、肠道运动功能进行性障碍以及肠神经节减少。我们设计本研究以调查NEDL2在正常人类结肠和先天性巨结肠(HSCR)中的表达情况。

方法

在拖出式手术时收集HSCR组织标本(n = 10),并分为无神经节段和有神经节段。结肠对照样本(n = 10)取自肛门闭锁患者结肠造口关闭时。使用共聚焦显微镜观察NEDL2的免疫标记以评估蛋白质分布,同时进行蛋白质印迹分析以量化NEDL2蛋白表达。

结果

共聚焦显微镜显示,在对照组和有神经节标本的黏膜下层、肌间神经丛和平滑肌中,NEDL2免疫反应性与肠肌间神经丛ICC和神经元共定位,而在无神经节标本中NEDL2免疫反应性明显降低。蛋白质印迹显示正常对照组和HSCR有神经节区域中NEDL2蛋白水平较高,而HSCR无神经节区域中NEDL2蛋白表达明显降低。

结论

我们首次报道了NEDL2在人类结肠中的表达。无神经节结肠中NEDL2表达降低表明NEDL2可能在HSCR的病理生理学中起作用。

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