Dose‐dependent density change of lens epithelial cells after in vivo UVR exposure

Abstract

AbstractIntroductionOur research group focuses on the mechanism of ultraviolet radiation (UVR) induced lens damage. Posterior capsule opacification (PCO) is the most common complication for cataract surgery. PCO results from the growth and abnormal proliferation of lens epithelial cells (LECs) on the posterior capsule. Lens epithelium is the first target for toxic factors such as ultraviolet radiation. UVR‐300 nm (UVR‐B) is especially an important risk factor for cataract development. Our previous findings show that exposure to UVR‐B can damage the lens epithelium, affect the expression of proteins, induce apoptosis and lead to cataract formation. Therefore, it is possible to prevent PCO by sufficient dose exposure of ultraviolet radiation to residual lens epithelial cells after cataract surgery.PurposeTo determine the effect of different doses of UVR on the distribution of lens epithelial cells (LECs).MethodsAltogether, 40 Sprague Dawley rats were unilaterally exposed in vivo to 1, 3, 6 and 8 kJ/m2 UVR‐300 nm for 15 min. One week after UVR exposure, exposed and contralateral non‐exposed lenses were removed. One midsagittal section from each lens was stained with DAPI for fluorescence microscopy in order to determine the spatial distribution of LECs.ResultsThe LECs density difference between exposed and contralateral non‐exposed eyes at exposure dose of 1, 3, 6 and 8 kJ/m2 was estimated as a CI (95%), −0.1 ± 2.1, 0.1 ± 3.0, −4.1 ± 1.4 and −2.9 ± 2.7 Cell μm−1 10−2, respectively. Data was fit to a linear model considering the initial density difference at 0. The inclination coefficient was estimated as CI (95%), −0.4 ± 0.1 Cell μm kJ−1 1010.ConclusionUVR‐300 nm induces significant LECs density decrease at exposure dose ≥6 kJ/m2. With fitting to a linear model the evolution of dose‐cell density dependence can be determined.