Department of Cellular Biology & Anatomy, Augusta University, 1120 15th Street, Augusta, GA 30912, USA.
Center for Biotechnology and Genomic Medicine, Augusta University, 1120 15th Street, Augusta, GA 30912, USA.
Cells. 2023 Nov 22;12(23):2681. doi: 10.3390/cells12232681.
Keratoconus (KC) is characterized by localized, central thinning and cone-like protrusion of the cornea. Its precise etiology remains undetermined, although both genetic and environmental factors are known to contribute to disease susceptibility. Due to KC's complex nature, there is currently no ideal animal model to represent both the corneal phenotype and underlying pathophysiology. Attempts to establish a KC model have involved mice, rats, and rabbits, with some additional novel animals suggested. Genetic animal models have only been attempted in mice. Similarly, spontaneously occurring animal models for KC have only been discovered in mice. Models generated using chemical or environmental treatments have been attempted in mice, rats, and rabbits. Among several methods used to induce KC in animals, ultraviolet radiation exposure and treatment with collagenase are some of the most prevalent. There is a clear need for an experimental model animal to elucidate the underlying mechanisms behind the development and progression of keratoconus. An appropriate animal model could also aid in the development of treatments to slow or arrest the disorder.
圆锥角膜(KC)的特征是角膜局部、中央变薄和圆锥形突出。其确切病因尚不清楚,尽管已知遗传和环境因素都有助于疾病易感性。由于 KC 的复杂性,目前还没有理想的动物模型能够同时代表角膜表型和潜在的病理生理学。建立 KC 模型的尝试涉及小鼠、大鼠和兔子,还提出了一些其他新的动物。遗传动物模型仅在小鼠中进行了尝试。同样,KC 的自发性动物模型也仅在小鼠中发现。使用化学或环境处理生成的模型已在小鼠、大鼠和兔子中进行了尝试。在用于诱导动物 KC 的几种方法中,紫外线辐射暴露和胶原酶处理是最常见的方法之一。显然需要一种实验模型动物来阐明圆锥角膜发展和进展背后的潜在机制。合适的动物模型也可以帮助开发减缓或阻止该疾病的治疗方法。