Kobayashi H, Yamataka A, Fujimoto T, Lane G J, Miyano T
Department of Pediatric Surgery, Juntendo University School of Medicine, Tokyo, Japan.
J Pediatr Surg. 1999 Apr;34(4):543-8. doi: 10.1016/s0022-3468(99)90069-6.
BACKGROUND/PURPOSE: In Hirschsprung's disease (HD), the aganglionic bowel is characterized by the presence of hypertrophic nerve trunks and increased numbers of adrenergic and cholinergic nerve fibers. Intestinal neuronal dysplasia (IND), if associated with HD, occurs proximal to the aganglionic segment in HD, and is characterized by dysplasia of parasympathetic nerves, hyperganglionosis, and giant ganglia. However, the cause of such abnormalities in HD and IND is unclear. Recent reports that mast cells (MC) have been observed in direct contact with nerve fibers generally, suggest that MC are essential for nerve growth and repair. MC synthesize, store, and release nerve growth factor (NGF). NGF supports the development and functional maintenance of sympathetic and cholinergic neurons. The aim of this study was to examine the colonic distribution of MC with respect to nerves in HD and HD associated with IND.
MC and NGF were examined immunohistochemically in ganglionic, transitional, and aganglionic segments of colon from 20 patients with HD (five patients associated with IND) and 15 age-matched controls. MC were counted in each of five random fields using light microscopy (x100).
Interestingly, aganglionic and IND segments had large numbers of MC in all layers compared with ganglionic segments in HD patients and controls (P< .0001). The number of MC in transitional segments was significantly less compared with ganglionic segments in HD patients and controls (P< .01). MC stained positively for NGF, and some were found in contact with abnormal hypertrophic nerve trunks in HD and giant ganglia in IND.
MC may cause hypertrophic nerve trunks and giant ganglia by releasing NGF and also may be an important factor in the excessive development of cholinergic and adrenergic nerve fibers in HD and IND.
背景/目的:在先天性巨结肠(HD)中,无神经节肠段的特征是存在肥厚的神经干以及肾上腺素能和胆碱能神经纤维数量增加。如果与HD相关,肠道神经元发育异常(IND)发生在HD无神经节段的近端,其特征是副交感神经发育异常、神经节增生和巨大神经节。然而,HD和IND中这些异常的原因尚不清楚。最近的报道表明,一般观察到肥大细胞(MC)与神经纤维直接接触,提示MC对神经生长和修复至关重要。MC合成、储存和释放神经生长因子(NGF)。NGF支持交感神经和胆碱能神经元的发育和功能维持。本研究的目的是检查HD以及与IND相关的HD中MC相对于神经的结肠分布情况。
对20例HD患者(5例与IND相关)和15例年龄匹配的对照者的结肠神经节段、过渡段和无神经节段进行免疫组织化学检测,以检测MC和NGF。使用光学显微镜(×100)在五个随机视野中分别计数MC。
有趣的是,与HD患者和对照者的神经节段相比,无神经节段和IND段各层中的MC数量均较多(P<0.0001)。与HD患者和对照者的神经节段相比,过渡段中的MC数量明显较少(P<0.01)。MC对NGF染色呈阳性,并且在HD中发现一些与异常肥厚的神经干接触,在IND中与巨大神经节接触。
MC可能通过释放NGF导致神经干肥厚和巨大神经节形成,并且可能是HD和IND中胆碱能和肾上腺素能神经纤维过度发育的一个重要因素。