Visser R, Arends J W, Leigh I M, Bosman F T
Department of Pathology, University Hospital, State University of Limburg, Maastricht, The Netherlands.
J Pathol. 1993 Jul;170(3):285-90. doi: 10.1002/path.1711700311.
We studied the distribution of type IV collagen and type VII collagen in the basement membranes of normal mucosa of the colon, adenomas, and adenocarcinomas using immunoperoxidase and immunofluorescence techniques. In normal mucosa, we found regular type IV collagen-positive basement membranes, lining vascular structures and mucosal epithelia. These basement membranes, however, lacked type VII collagen. In adenomas of the colon, intact basement membranes were observed through type IV collagen staining. Type VII collagen staining was also detected, but only in connection with dysplastic epithelium. Adjacent to the dysplastic epithelium in adenomas, histologically normal epithelium also showed type VII collagen staining along the basement membrane, but this was restricted to the epithelium of the luminal surface. These areas were also investigated for expression of keratins 8, 18, and 19, and keratins 5 and 8 (monoclonal antibodies NCL-5D3 and RCK 102, respectively), but altered differentiation was not detected using this technique. In adenocarcinomas of the colon, type IV collagen was irregularly deposited in the basement membrane of neoplastic tubules. Type VII collagen staining was detected only in well or moderately differentiated carcinomas and in higher amounts. Our findings therefore reveal a transient expression of type VII collagen in the transition of dysplastic epithelium into carcinoma, suggesting the involvement of type VII collagen in the process of early invasion.
我们使用免疫过氧化物酶和免疫荧光技术研究了Ⅳ型胶原和Ⅶ型胶原在结肠正常黏膜、腺瘤及腺癌基底膜中的分布。在正常黏膜中,我们发现Ⅳ型胶原阳性的基底膜排列规则,衬于血管结构和黏膜上皮。然而,这些基底膜缺乏Ⅶ型胶原。在结肠腺瘤中,通过Ⅳ型胶原染色观察到完整的基底膜。也检测到了Ⅶ型胶原染色,但仅与发育异常的上皮有关。在腺瘤中,与发育异常上皮相邻的组织学正常上皮在基底膜处也显示Ⅶ型胶原染色,但仅限于腔面的上皮。还对这些区域进行了角蛋白8、18和19以及角蛋白5和8(分别为单克隆抗体NCL - 5D3和RCK 102)表达的研究,但使用该技术未检测到分化改变。在结肠腺癌中,Ⅳ型胶原不规则地沉积在肿瘤小管的基底膜中。仅在高分化或中分化癌中检测到Ⅶ型胶原染色,且含量较高。因此,我们的研究结果揭示了Ⅶ型胶原在发育异常上皮向癌转变过程中的短暂表达,提示Ⅶ型胶原参与早期侵袭过程。