Ishizaki M, Shimoda M, Wakamatsu K, Ogro T, Yamanaka N, Kao C W, Kao W W
Department of Pathology, Nippon Medical School, Tokyo, Japan.
Curr Eye Res. 1997 Apr;16(4):339-48. doi: 10.1076/ceyr.16.4.339.10684.
Corneal wound healing frequently leads to the formation of opaque scar tissue. We examined whether stromal fibroblastic cells of injured corneas express collagen IV and contributes to the formation of a basal lamina-like structure.
Rabbits were anesthetized, and central corneal alkali burn (8 mm in diameter; 1 M NaOH, 1 min) or laceration (8 mm long) were produced. The injured corneas, which had healed for 1, 7, 21 and 45 days, were subjected to histological and immunohistochemical studies with goat anti-collagen IV antibodies, using light and electron microscopy, and in situ hybridization with an antisense digoxigenin-labeled riboprobe of collagen alpha 1(IV) mRNA. For comparison, twenty-day-old fetal corneas were subjected to immunohistochemical study and transmission electron microscopy (TEM).
TEM examinations revealed that the stromal collagenous matrix was organized in orthogonal lamellae during corneal development, whereas that of alkali-burned cornea, which had healed for 3 weeks, was disorganized. The stroma of twenty-day-old fetal cornea was not labeled by the anti-collagen IV antibodies. In contrast, one week after injury, specific collagen IV immunostaining was detected in the injured stroma. As the healing proceeded (21-45 days), the antibodies reacted with fibroblastic cells and the extracellular matrix of scar tissues located in the anterior portion of alkali-burned corneas, as well as the posterior portion of lacerated corneas. The middle portion of the stromal tissues was weakly labeled by the anti-collagen IV antibodies with the exception of the blood vessel wall. Immuno-electron microscopic study showed that collagen IV and fibronectin were closely associated with the fibroblastic cells. In situ hybridization demonstrated that epithelial and endothelial cells and fibroblastic cells in the wounded corneal stroma and retro-corneal membrane expressed alpha 1(IV) mRNA, whereas in normal corneas the expression of alpha 1(IV) mRNA was limited to epithelial and endothelial cells.
The enhanced expression of collagen IV by the fibroblastic cells in the stroma of injured corneas is consistent with the notion that they may contribute to the formation of basal lamina-like structures in injured corneas.
角膜伤口愈合常导致不透明瘢痕组织形成。我们研究了受伤角膜的基质成纤维细胞是否表达IV型胶原并促成类基底膜结构的形成。
将兔子麻醉后,制作中央角膜碱烧伤(直径8毫米;1 M氢氧化钠,1分钟)或撕裂伤(长8毫米)。对愈合1、7、21和45天的受伤角膜进行组织学和免疫组织化学研究,使用山羊抗IV型胶原抗体,采用光学和电子显微镜观察,并与地高辛配基标记的胶原α1(IV) mRNA反义核糖探针进行原位杂交。为作比较,对20日龄胎儿角膜进行免疫组织化学研究和透射电子显微镜(TEM)检查。
TEM检查显示,角膜发育过程中基质胶原基质呈正交板层状排列,而愈合3周的碱烧伤角膜的基质胶原基质排列紊乱。20日龄胎儿角膜基质未被抗IV型胶原抗体标记。相反,受伤1周后,在受伤基质中检测到特异性IV型胶原免疫染色。随着愈合进程(21 - 45天),抗体与碱烧伤角膜前部以及撕裂伤角膜后部瘢痕组织中的成纤维细胞和细胞外基质发生反应。除血管壁外,基质组织中部被抗IV型胶原抗体弱阳性标记。免疫电子显微镜研究表明,IV型胶原和纤连蛋白与成纤维细胞紧密相关。原位杂交显示,受伤角膜基质和角膜后膜中的上皮细胞、内皮细胞和成纤维细胞表达α1(IV) mRNA,而正常角膜中α1(IV) mRNA的表达仅限于上皮细胞和内皮细胞。
受伤角膜基质中的成纤维细胞增强表达IV型胶原,这与它们可能促成受伤角膜中类基底膜结构形成的观点一致。