新生儿坏死性小肠结肠炎肠神经系统的全载免疫组织化学改变。

T Wedel, H J Krammer, W Kühnel, W Sigge
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引用次数: 0

摘要

新生儿坏死性小肠结肠炎(NNEC)的病理学报道很少考虑其对肠神经系统(ENS)的影响。因此,本研究的目的是通过全载免疫组织化学方法对肠壁三个神经节丛内的神经病理病变进行二维评估。切除的受急性NNEC影响的回肠和结肠部分经免疫组织化学处理,使用抗神经元(蛋白基因产物9.5)和胶质(蛋白S-100,胶质纤维酸性蛋白)蛋白的抗体。对肌肠丛和外粘膜下丛的检查显示,胶质细胞明显减少,同时神经细胞逐渐退化,这两种发现主要出现在反肠周,缺血性病变往往首先出现。神经组织损伤最严重的部位为神经丛粘膜下内肌,与粘膜损伤的深度有关。受损的神经节看起来像“空篮子”(残留的缠结),里面装着退化的神经和胶质细胞。考虑到肠道血管血液供应的解剖结构,神经病理病变的特征地形进一步支持了不同病理因素级联中的缺血性事件,最终导致NNEC。此外,ENS的改变及其对肠道运动和神经免疫相互作用的潜在不利影响可能是NNEC复杂发病机制的原因,这仍是一个有待进一步研究的领域。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Alterations of the enteric nervous system in neonatal necrotizing enterocolitis revealed by whole-mount immunohistochemistry.

Pathology reports on neonatal necrotizing enterocolitis (NNEC) rarely consider its effects on the enteric nervous system (ENS). Thus, the aim of this study has been to perform a two-dimensional assessment of neuropathologic lesions within the three ganglionated plexuses of the intestinal wall by means of whole-mount immunohistochemistry. Resected segments of ileum and colon affected by acute NNEC were submitted to immunohistochemical procedures using antibodies against neuronal (protein gene product 9.5) and glial (protein S-100, glial fibrillary acidic protein) proteins. Examination of the myenteric plexus and external submucosal plexus revealed a noticeable reduction in glial cells concomitant with the gradual deterioration of nerve cells, both findings predominating in the antimesenteric intestinal circumference, where ischemic lesions tend to appear first. The most severe damage of nervous tissue was observed in the plexus submucosus internus dependent on the depth of mucosal injury. The destroyed ganglia appeared like "empty baskets" (residual tangles) and housed deteriorated nerve and glial cells. Taking the anatomy of the intestinal vascular blood supply into consideration, the characteristic topography of neuropathologic lesions gives further support to an ischemic event within the cascade of different pathogenetic factors culminating in NNEC. Moreover, the demonstrated alterations of the ENS and their potential adverse effects on intestinal motility and neuroimmunologic interactions may contribute to the complex pathogenesis of NNEC, which remains a field of further investigation.

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