Identification of Differential Gene Expression Pattern in Lens Epithelial Cells Derived from Cataractous and Noncataractous Lenses of Shumiya Cataract Rat

• Published in: BioMed research international Vol. 2020; no. 2020; pp. 1 - 9
• Main Authors: Kubo, Eri, Singh, Dhirendra P., Ishigaki, Yasuhito, Nakamura, Yuka, Shibata, Teppei, Ishida, Hidetoshi, Sasaki, Hiroshi
• Format: Journal Article
• Language: English
• Published: Cairo, Egypt Hindawi Publishing Corporation 2020; Hindawi; Hindawi Limited
• Subjects: Age; Animals; Cataract - genetics; Cataracts; Cell differentiation; Cell growth; Cholesterol; Congenital diseases; Crystallin; Deoxyribonuclease; Deoxyribonuclease II; Differentiation; Disease; DNA microarrays; Epithelial cells; Epithelial Cells - pathology; Farnesyl-diphosphate farnesyltransferase; Farnesyltransferase; Gene expression; Gene Expression Profiling; Genes; Heat shock proteins; Homeostasis; Laboratory animals; Lanosterol; Lanosterol synthase; Lens, Crystalline - cytology; Lens, Crystalline - pathology; Lenses; Mutation; Opacity; Oxidative stress; Proteins; Rats, Inbred Strains; Reproducibility of Results; Statistical analysis; Variance analysis; Japan
• ISSN: 2314-6133; 2314-6141
• DOI: 10.1155/2020/7319590

The Shumiya cataract rat (SCR) is a model for hereditary cataract. Two-thirds of these rats develop lens opacity within 10-11 weeks. Onset of cataract is attributed to the synergetic effect of lanosterol synthase (Lss) and farnesyl-diphosphate farnesyltransferase 1 (Fdft1) mutant alleles that lead to cholesterol deficiency in the lenses, which in turn adversely affects lens biology including the growth and differentiation of lens epithelial cells (LECs). Nevertheless, the molecular events and changes in gene expression associated with the onset of lens opacity in SCR are poorly understood. In the present study, a microarray-based approach was employed to analyze comparative gene expression changes in LECs isolated from the precataractous and cataractous stages of lenses of 5-week-old SCRs. The changes in gene expression observed in microarray results in the LECs were further validated using real-time reverse transcribed quantitative PCR (RT-qPCR) in 5-, 8-, and 10-week-old SCRs. A mild posterior and cortical opacity was observed in 5-week-old rats. Expressions of approximately 100 genes, including the major intrinsic protein of the lens fiber (Mip and Aquaporin 0), deoxyribonuclease II beta (Dnase2B), heat shock protein B1 (HspB1), and crystallin γ (γCry) B, C, and F, were found to be significantly downregulated (0.07-0.5-fold) in rat LECs derived from cataract lenses compared to that in noncataractous lenses (control). Thus, our study was aimed at identifying the gene expression patterns during cataract formation in SCRs, which may be responsible for cataractogenesis in SCR. We proposed that cataracts in SCR are associated with reduced expression of these lens genes that have been reported to be related with lens fiber differentiation. Our findings may have wider implications in understanding the effect of cholesterol deficiency and the role of cholesterol-lowering therapeutics on cataractogenesis.