Hirsch-Marie H, Loisillier F, Touboul J P, Burtin P
Lab Invest. 1976 Jun;34(6):623-32.
Gastric pepsinogens were studied by immunoenzymologic and immunohistochemical methods in non-cancerous adult gastric mucosa, in fetal stomach, and in gastric carcinomas. In noncancerous adult mucosa, immunoenzymologic methods showed that pepsinogen II (previously called Pg I-II) was found mostly in fundic or mediogastric extracts, whereas Pg IV was predominant in antropyloric extracts. Pg II was localized by immunofluorescence techniques in the chief cells of deep glands found near the muscularis. Pg II was localized by immunofluorescence techniques in the chief cells of deep glands found near the muscularis. Pg III was present in the superficial zone of deep glands and Pg IV in the surface epithelium and in the superficial glands of the mucosa. In fetal stomach, only Pg IV (which we called the "fetal pepsinogen") was identified by standard immunoelectrophoresis. It was localized by immunofluorescence in the superficial epithelium. However, bidimensional immunoelectrophoresis and immunofluorescence did reveal low levels of Pg II and Pg III by the 8th or 9th week of ontogenesis. Pg II and Pg III were localized in the rudimentary glands near the superficial epithelium. Important differences were noted when gastric carcinomas were compared with normal mucosa. Pg II or Pg III were often absent in the tumor extracts, but Pg IV was regularly and, at times, exclusively identified regardless of the location of the tumor. By immunofluorescence Pg IV was often the only pepsinogen that was characterized in dedifferentiated cancerous cells; this was also true of the calciform cells of some metaplastic gastric mucosa. Pg III was observed rarely, and Pg II never, in cancerous cells. The biochemical modifications of the cancerous tissue closely resemble those of fetal tissue.
采用免疫酶学和免疫组织化学方法,对非癌成人胃黏膜、胎儿胃以及胃癌中的胃蛋白酶原进行了研究。在非癌成人黏膜中,免疫酶学方法显示,胃蛋白酶原II(以前称为Pg I-II)主要存在于胃底或胃中部提取物中,而Pg IV在胃窦提取物中占主导地位。通过免疫荧光技术发现,Pg II定位于肌层附近深层腺体的主细胞中。Pg III存在于深层腺体的表层区域,Pg IV存在于黏膜的表面上皮和浅表腺体中。在胎儿胃中,通过标准免疫电泳仅鉴定出Pg IV(我们称之为“胎儿胃蛋白酶原”)。通过免疫荧光将其定位于表面上皮中。然而,双向免疫电泳和免疫荧光确实显示,在个体发育的第8或9周时,Pg II和Pg III的水平较低。Pg II和Pg III定位于表面上皮附近的原始腺体中。将胃癌与正常黏膜进行比较时,发现了重要差异。肿瘤提取物中常常缺乏Pg II或Pg III,但无论肿瘤位于何处,Pg IV都能被定期鉴定出来,有时甚至是唯一被鉴定出来的。通过免疫荧光,Pg IV常常是去分化癌细胞中唯一鉴定出的胃蛋白酶原;一些化生胃黏膜的杯状细胞也是如此。在癌细胞中很少观察到Pg III,从未观察到Pg II。癌组织的生化改变与胎儿组织极为相似。