Animal Models for the Study of Keratoconus

被引:6
|
作者
Hadvina, Rachel [1 ,2 ]
Estes, Amy [3 ,4 ]
Liu, Yutao [1 ,2 ,3 ]
机构
[1] Augusta Univ, Dept Cellular Biol & Anat, 1120 15th St, Augusta, GA 30912 USA
[2] Augusta Univ, Ctr Biotechnol & Genom Med, 1120 15th St, Augusta, GA 30912 USA
[3] Augusta Univ, James & Jean Culver Vis Discovery Inst, Med Coll Georgia, 1120 15th St, Augusta, GA 30912 USA
[4] Augusta Univ, Dept Ophthalmol, Augusta, GA 30912 USA
关键词
keratoconus; cornea; animal models; mice; rabbit; keratocytes; HEPATOCYTE GROWTH-FACTOR; GENOME-WIDE ASSOCIATION; ENDO-BETA-GALACTOSIDASE; ULTRAVIOLET-RADIATION; CORNEAL THICKNESS; BIOMECHANICAL PROPERTIES; COLLAGEN FIBRILS; RAT CORNEA; POP-EYE; MOUSE;
D O I
10.3390/cells12232681
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
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.
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页数:23
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