Adenomatous Polyposis Coli Mutation Leads to Myopia Development in Mice

• Published in: PloS one Vol. 10; no. 10; p. e0141144
• Main Authors: Liu, Zhen, Qiu, Fangfang, Li, Jing, Zhu, Zhenzhen, Yang, Wenzhao, Zhou, Xiangtian, An, Jianhong, Huang, Furong, Wang, Qiongsi, Reinach, Peter S, Li, Wei, Chen, Wensheng, Liu, Zuguo
• Format: Journal Article
• Language: English
• Published: United States Public Library of Science 23.10.2015; Public Library of Science (PLoS)
• Subjects: Adenomatous polyposis coli; Adenomatous polyposis coli protein; Adenomatous Polyposis Coli Protein - genetics; Adenomatous Polyposis Coli Protein - metabolism; Animals; Biometrics; Cell cycle; Cell proliferation; Collagen; Collagen (type I); Collagen Type I - genetics; Collagen Type I - metabolism; Collagens; College campuses; Colorectal cancer; Complications; Developmental stages; Disease Models, Animal; Dopamine; Familial adenomatous polyposis; Gelatinase A; Gelatinase B; Gene expression; Gene Expression Regulation; Genetic disorders; Humans; Hydroxylase; Incidence; Laboratories; Male; Matrix Metalloproteinase 2 - genetics; Matrix Metalloproteinase 2 - metabolism; Matrix Metalloproteinase 9 - genetics; Matrix Metalloproteinase 9 - metabolism; Mice; Mice, Knockout; Mutation; Myopia; Myopia - genetics; Myopia - metabolism; Myopia - pathology; Optical Coherence Tomography; Optometry; Pathogenesis; Photorefraction; Polyposis coli; Polyps; Refraction; Refraction, Ocular; Retina; Retina - metabolism; Retina - pathology; Rodents; Science; Sclera - metabolism; Sclera - pathology; Stem cells; Tomography, Optical Coherence; Tyrosine; Tyrosine 3-monooxygenase; Tyrosine 3-Monooxygenase - genetics; Tyrosine 3-Monooxygenase - metabolism; Vision, Ocular; Vitreous Body - metabolism; Vitreous Body - pathology; China
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0141144

Myopia incidence in China is rapidly becoming a very serious sight compromising problem in a large segment of the general population. Therefore, delineating the underlying mechanisms leading to myopia will markedly lessen the likelihood of other sight compromising complications. In this regard, there is some evidence that patients afflicted with familial adenomatous polyposis (FAP), havean adenomatous polyposis coli (APC) mutation and a higher incidence of myopia. To clarify this possible association, we determined whether the changes in pertinent biometric and biochemical parameters underlying postnatal refractive error development in APCMin mice are relevant for gaining insight into the pathogenesis of this disease in humans. The refraction and biometrics in APCMin mice and age-matched wild-type (WT) littermates between postnatal days P28 and P84 were examined with eccentric infrared photorefraction (EIR) and customized optical coherence tomography (OCT). Compared with WT littermates, the APCMin mutated mice developed myopia (average -4.64 D) on P84 which was associated with increased vitreous chamber depth (VCD). Furthermore, retinal and scleral changes appear in these mice along with: 1) axial length shortening; 2) increased retinal cell proliferation; 3) and decreased tyrosine hydroxylase (TH) expression, the rate-limiting enzyme of DA synthesis. Scleral collagen fibril diameters became heterogeneous and irregularly organized in the APCMin mice. Western blot analysis showed that scleral alpha-1 type I collagen (col1α1) expression also decreased whereas MMP2 and MMP9 mRNA expression was invariant. These results indicate that defective APC gene function promotes refractive error development. By characterizing in APCMin mice ocular developmental changes, this approach provides novel insight into underlying pathophysiological mechanisms contributing to human myopia development.