Ballouhey Quentin, Richard Laurence, Fourcade Laurent, Ben Rhaiem Ines, Vallat Jean Michel, Sturtz Franck, Bourthoumieu Sylvie
EA6309 peripheral neuropathy, University of Medecine, Limoges, France.
Department of pediatric surgery, University Hospital, Limoges, France.
PLoS One. 2017 Nov 1;12(11):e0186507. doi: 10.1371/journal.pone.0186507. eCollection 2017.
Intestinal atresia, a rare congenital condition, is often associated with intestinal motility disorders despite adequate neonatal surgery. Previous studies have focused on changes in the enteric nervous system (ENS). We hypothesized that other components of the digestive tract could be involved in this condition.
In a rat model of surgically-induced intestinal obstruction, a transcriptome analysis was performed to measure the global gene expression. Then, analyzes were focused on genes expressed in ENS and neuroendocrine cells. Rat fetus small intestines at different developmental stages (ED15, ED17, ED19 and ED21, (n = 22)) were studied as controls and compared to the upper and lower segments of small intestines from rat fetuses with surgically-induced obstruction (n = 14; ligature at ED18). The gene expression pattern was confirmed by immunohistochemistry, electron microscopy and RT-qPCR.
From ED15 to ED21, there was a physiological decrease in the gene expression of ENS markers and an increase in that of neuroendocrine genes. Regarding operated embryos, the changes in global gene expression were significantly higher in the proximal segment compared to the distal segment (18% vs. 9%). More precisely, a decrease in ENS gene expression and an increase in neuroendocrine gene expression were observed in the proximal segment compared to controls, indicating an accelerated maturation pattern. Immunohistochemistry and electron microscopy confirmed these findings.
Fetal intestinal obstruction seems to induce an accelerated maturation in the proximal segment. Moreover, neuroendocrine cells undergo significant unexpected changes, suggesting that ENS changes could be associated with other changes to induce intestinal motility disorders.
肠闭锁是一种罕见的先天性疾病,尽管新生儿手术充分,但常伴有肠道运动障碍。以往的研究主要集中在肠神经系统(ENS)的变化。我们推测消化道的其他成分可能与这种情况有关。
在手术诱导的肠梗阻大鼠模型中,进行转录组分析以测量整体基因表达。然后,分析集中在ENS和神经内分泌细胞中表达的基因。研究了不同发育阶段(胚胎第15天、第17天、第19天和第21天,(n = 22))的大鼠胎儿小肠作为对照,并与手术诱导梗阻的大鼠胎儿小肠的上段和下段进行比较(n = 14;胚胎第18天结扎)。通过免疫组织化学、电子显微镜和逆转录定量聚合酶链反应(RT-qPCR)证实基因表达模式。
从胚胎第15天到第21天,ENS标志物的基因表达呈生理性下降,而神经内分泌基因的表达则增加。对于手术胚胎,近端段的整体基因表达变化明显高于远端段(18%对9%)。更确切地说,与对照组相比,近端段观察到ENS基因表达下降,神经内分泌基因表达增加,表明成熟模式加速。免疫组织化学和电子显微镜证实了这些发现。
胎儿肠梗阻似乎诱导近端段成熟加速。此外,神经内分泌细胞发生了显著的意外变化,表明ENS变化可能与其他变化相关,从而导致肠道运动障碍。