Kato H, Yamamoto T, Yamamoto H, Ohi R, So N, Iwasaki Y
Department of Pediatric Surgery, Tohoku University School of Medicine, Sendai, Japan.
J Pediatr Surg. 1990 May;25(5):514-9. doi: 10.1016/0022-3468(90)90563-o.
The enteric nervous system (ENS) is composed of two distinct neural components, extrinsic and intrinsic, and its supporting cells uniquely possess some characteristics of both central nervous system (CNS) astrocytes and peripheral nervous system (PNS) Schwann cells. To provide further insight into the neural defects in Hirschsprung's disease, the supporting cells in biopsied normal gut, ganglionic, and aganglionic segments from six cases of Hirschsprung's disease were investigated immunocytochemically for localization of three neuroglial markers, glial fibrillary acidic protein (GFAP), S-100 protein, and glutamine synthetase (GS), by the avidin-biotin-horseradish peroxidase complex method applied to free-floating thick cryostat sections. In normal control gut and ganglionic segments of Hirschsprung's colon, all of the GFAP, S-100, and GS were expressed strongly by the supporting cells of the myenteric and submucosal plexuses, interconnecting nerve fiber bundles of the plexuses, and fine nerve strands in the muscular layer. The nerve bundles of the subserosa merging into the muscular layer were also immunoreactive for GFAP and S-100, but negative or only faintly positive for GS. On the other hand, aberrantly proliferated nerve bundles in the aganglionic segment of the Hirschsprung's colon were accompanied by supporting cells strongly positive for GFAP and S-100, but negative or faintly positive for GS. These results indicate that the supporting cells of the enteric neurons proper, enteric glia, express GFAP, S-100, and GS, whereas the supporting cells of the extrinsic components, which accompany PNS axons, are negative or very weakly positive for GS. Thus, GS immunocytochemistry may delineate intrinsic and extrinsic neural components in the ENS, and may provide an important clue for differential diagnosis of Hirschsprung's disease.
肠神经系统(ENS)由两个不同的神经成分组成,即外在成分和内在成分,其支持细胞独特地具有中枢神经系统(CNS)星形胶质细胞和外周神经系统(PNS)雪旺细胞的一些特征。为了进一步深入了解先天性巨结肠症的神经缺陷,采用抗生物素蛋白-生物素-辣根过氧化物酶复合物法,对6例先天性巨结肠症患者活检的正常肠段、神经节段和无神经节段的支持细胞进行免疫细胞化学研究,以定位三种神经胶质标志物,即胶质纤维酸性蛋白(GFAP)、S-100蛋白和谷氨酰胺合成酶(GS),该方法应用于冷冻切片的游离厚切片。在正常对照肠段和先天性巨结肠症结肠的神经节段,肌间神经丛和黏膜下神经丛的支持细胞、神经丛相互连接的神经纤维束以及肌层中的细神经束均强烈表达GFAP、S-100和GS。浆膜下汇入肌层的神经束对GFAP和S-100也呈免疫反应,但对GS呈阴性或仅弱阳性。另一方面,先天性巨结肠症结肠无神经节段中异常增生的神经束伴有对GFAP和S-100呈强阳性但对GS呈阴性或弱阳性的支持细胞。这些结果表明,肠神经元本身的支持细胞,即肠神经胶质细胞,表达GFAP、S-100和GS,而伴随PNS轴突的外在成分的支持细胞对GS呈阴性或非常弱阳性。因此,GS免疫细胞化学可能有助于区分ENS中的内在和外在神经成分,并可能为先天性巨结肠症的鉴别诊断提供重要线索。