Cho H I, Covington H I, Cintron C
Eye Research Institute, Boston, MA 02114.
Invest Ophthalmol Vis Sci. 1990 Jun;31(6):1096-102.
We have localized type VI collagen in normal developing and corneal scar tissue. Indirect immunofluorescence showed that type VI collagen was distributed throughout the normal stroma and most of the scar. No fluorescence was detected along the posterior margin of the scar and in a retrocorneal membrane continuous with the scar. Since the corneal endothelium in rabbits contributes to the formation of scar tissue and retrocorneal membrane, our observations suggest that the endothelium does not synthesize type VI collagen. Indirect immunoelectron microscopy showed that type VI collagen was located abundantly between collagen fibrils as fine filamentous structures containing beads with a periodicity of 100 nm, consistent with published observations of other tissues. Because these filaments are more prominent when stained with ruthenium red, and predigestion of tissue with Chondroitinase ABC enhances binding of monoclonal antibody to type VI collagen, proteoglycans probably are associated with this collagen in the cornea. Ultrastructural observations supported by previous biochemical analyses show that the proportion of type VI collagen to fibrillar collagen is smaller in scar tissue compared with fetal cornea. The abundance of type VI collagen and its distribution and association with proteoglycans in rabbit corneal tissues suggest that this macromolecule plays a role in the tensile strength and transparency of the stroma.
我们已在正常发育的角膜和角膜瘢痕组织中定位了VI型胶原蛋白。间接免疫荧光显示,VI型胶原蛋白分布于整个正常基质和大部分瘢痕组织中。在瘢痕组织的后缘以及与瘢痕相连的角膜后膜中未检测到荧光。由于兔角膜内皮细胞参与瘢痕组织和角膜后膜的形成,我们的观察结果表明内皮细胞不合成VI型胶原蛋白。间接免疫电子显微镜显示,VI型胶原蛋白大量位于胶原纤维之间,呈细丝状结构,含有周期为100nm的珠状结构,这与其他组织已发表的观察结果一致。因为这些细丝在用钌红染色时更为明显,并且用软骨素酶ABC对组织进行预消化可增强单克隆抗体与VI型胶原蛋白的结合,所以蛋白聚糖可能与角膜中的这种胶原蛋白相关。先前生化分析支持的超微结构观察表明,与胎儿角膜相比,瘢痕组织中VI型胶原蛋白与纤维状胶原蛋白的比例较小。兔角膜组织中VI型胶原蛋白的丰富程度及其分布以及与蛋白聚糖的关联表明,这种大分子在基质的抗张强度和透明度方面发挥作用。