Walker Janice L, Bleaken Brigid M, Wolff Iris M, Menko A Sue
Pathology, Anatomy and Cell Biology, Thomas Jefferson University;
Pathology, Anatomy and Cell Biology, Thomas Jefferson University.
J Vis Exp. 2015 Jun 5(100):e52886. doi: 10.3791/52886.
The major impediment to understanding how an epithelial tissue executes wound repair is the limited availability of models in which it is possible to follow and manipulate the wound response ex vivo in an environment that closely mimics that of epithelial tissue injury in vivo. This issue was addressed by creating a clinically relevant epithelial ex vivo injury-repair model based on cataract surgery. In this culture model, the response of the lens epithelium to wounding can be followed live in the cells' native microenvironment, and the molecular mediators of wound repair easily manipulated during the repair process. To prepare the cultures, lenses are removed from the eye and a small incision is made in the anterior of the lens from which the inner mass of lens fiber cells is removed. This procedure creates a circular wound on the posterior lens capsule, the thick basement membrane that surrounds the lens. This wound area where the fiber cells were attached is located just adjacent to a continuous monolayer of lens epithelial cells that remains linked to the lens capsule during the surgical procedure. The wounded epithelium, the cell type from which fiber cells are derived during development, responds to the injury of fiber cell removal by moving collectively across the wound area, led by a population of vimentin-rich repair cells whose mesenchymal progenitors are endogenous to the lens. These properties are typical of a normal epithelial wound healing response. In this model, as in vivo, wound repair is dependent on signals supplied by the endogenous environment that is uniquely maintained in this ex vivo culture system, providing an ideal opportunity for discovery of the mechanisms that regulate repair of an epithelium following wounding.
理解上皮组织如何进行伤口修复的主要障碍在于缺乏合适的模型,难以在体外环境中对伤口反应进行追踪和操控,该体外环境需紧密模拟上皮组织在体内的损伤情况。基于白内障手术创建了一个具有临床相关性的上皮体外损伤修复模型,解决了这一问题。在这个培养模型中,可以在细胞的天然微环境中实时追踪晶状体上皮对损伤的反应,并且在修复过程中能够轻松操控伤口修复的分子介质。制备培养物时,从眼睛中取出晶状体,在晶状体前部做一个小切口,去除晶状体纤维细胞的内部物质。这个操作在晶状体后囊膜上形成一个圆形伤口,后囊膜是围绕晶状体的厚基底膜。纤维细胞附着的这个伤口区域紧邻一层连续的晶状体上皮细胞单层,在手术过程中该单层细胞与晶状体囊膜保持相连。受伤的上皮细胞是发育过程中纤维细胞的来源细胞类型,它通过一群富含波形蛋白的修复细胞的引导,集体迁移穿过伤口区域,对纤维细胞移除造成的损伤做出反应,这些修复细胞的间充质祖细胞是晶状体固有的。这些特性是正常上皮伤口愈合反应的典型特征。在这个模型中,如同在体内一样,伤口修复依赖于由内源性环境提供的信号,这种内源性环境在这个体外培养系统中得以独特维持,为发现调控上皮组织受伤后修复机制提供了理想机会。