Nickeleit V, Kaufman A H, Zagachin L, Dutt J E, Foster C S, Colvin R B
Department of Pathology, Massachusetts General Hospital, Boston 02114, USA.
Am J Pathol. 1996 Aug;149(2):549-58.
The cornea is a simple, nonvascularized structure, advantageous for studying the molecular components of epithelial and stromal wound repair. Fibronectin (Fn), of uncertain source and composition, accumulates in healing corneas. We postulated that local synthesis of Fn occurs, as exogenous plasma/tear-derived Fn, which lack the embryonic EIIIA and EIIIB segments, have no consistent beneficial effect on healing. Two contrasting corneal wounds were examined by in situ hybridization: a wound of the anterior stroma, basement membrane, and epithelium (anterior excimer laser keratectomy) and a superficial wound restricted to the epithelium that preserved the basement membrane (mechanical scrape). Both wounds heal without scarring. In normal corneas, only the endothelium had detectable Fn mRNA, containing the V and EIIIB domains, sporadically and at low levels. After anterior keratectomies, extensive expression of Fn mRNA occurred in a specific distribution that changed during the phases of healing. Before re-epithelialization (days 1 and 2) V+, EIIIA+, and EIIIB+ isoforms were diffusely found in stromal cells under and adjacent to the wound. After re-epithelialization (days 3 to 42) and reconstitution of laminin in the regenerating basement membrane zone, V+, EIIIA+, and EIIIB+ isoform synthesis was largely restricted to subepithelial stromal cells at the epithelial/stromal interface. In addition, the corneal epithelial cells focally expressed Fn mRNA. The endothelium showed increased levels of V+, EIIIA+, and EIIIB+ Fn mRNA in open and recently re-epithelialized wounds. At 12 weeks after keratectomy, Fn mRNA expression returned to control levels. In contrast, scrape wounds had only a modest increase of stromal and endothelial Fn mRNA (EIIIA+, EIIIB+, and V+) during the first 7 days and no evidence of epithelial Fn synthesis. Embryonic Fn isoforms are synthesized transiently by the cornea in response to even the most superficial wounds and are likely to be relevant to corneal healing and restoration of structure without scar formation.
角膜是一种简单的、无血管的结构,有利于研究上皮和基质伤口修复的分子成分。来源和组成不确定的纤连蛋白(Fn)在愈合的角膜中积累。我们推测Fn是局部合成的,因为缺乏胚胎EIIIA和EIIIB片段的外源性血浆/泪液来源的Fn对愈合没有一致的有益作用。通过原位杂交检查了两种截然不同的角膜伤口:前基质、基底膜和上皮的伤口(准分子激光原位角膜磨镶术)以及仅限于上皮且保留基底膜的浅表伤口(机械刮伤)。两种伤口均无瘢痕愈合。在正常角膜中,只有内皮细胞有可检测到的Fn mRNA,其含有V和EIIIB结构域,呈散在且低水平表达。在前板层角膜移植术后,Fn mRNA在愈合阶段发生变化的特定分布中广泛表达。在重新上皮化之前(第1天和第2天),V +、EIIIA +和EIIIB +亚型在伤口下方和相邻的基质细胞中弥漫性存在。重新上皮化后(第3至42天)以及再生基底膜区中层粘连蛋白的重建后,V +、EIIIA +和EIIIB +亚型的合成主要局限于上皮/基质界面的上皮下基质细胞。此外,角膜上皮细胞局部表达Fn mRNA。在开放和最近重新上皮化的伤口中,内皮细胞显示V +、EIIIA +和EIIIB + Fn mRNA水平升高。角膜移植术后12周,Fn mRNA表达恢复到对照水平。相比之下,刮伤伤口在最初7天内基质和内皮Fn mRNA(EIIIA +、EIIIB +和V +)仅适度增加,且无上皮Fn合成的证据。即使是最浅表的伤口,角膜也会短暂合成胚胎Fn亚型,这可能与角膜愈合和无瘢痕形成的结构恢复有关。