Galichanin Konstantin
Gullstrand lab, Section of Ophthalmology, Department of Neuroscience, Uppsala University, Uppsala, Sweden.
Acta Ophthalmol. 2017 Dec;95(8):834-838. doi: 10.1111/aos.13370. Epub 2017 Jan 13.
The aim of this study was to investigate in which part of the lens in vivo exposure to subthreshold dose of UVR-B radiation induces apoptosis.
Twenty 6-week-old female albino Sprague-Dawley rats were exposed to subthreshold dose (1 kJ/m ) of UVR-B unilaterally and killed at 120 hr after exposure. Lenses were enucleated and dissected on three regions: the lens epithelium, the cortex and the nucleus. The lens nucleus then was removed. Apoptosis markers p53 and caspase 3 were used to study apoptosis in the lens regions. qRT-PCR and Western blot were utilized to analyse the lenses.
TP53 and CASP3 mRNA expressions are increased in exposed lenses, both in the lens epithelium and in the cortex regions, in relation to non-exposed lenses. Expression of p53 protein is increased in exposed lens epithelium in relation to non-exposed lens epithelium. Caspase 3 protein is expressed in exposed lens epithelial cells, while it is not expressed in non-exposed lens epithelial cells. p53 and caspase 3 proteins are not expressed in either exposed nor non-exposed lens fibre cells.
Exposure to UVR-B increases mRNA transcription of apoptosis marker p53 in vivo in both regions of the lens and of apoptosis marker caspase 3 in the lens cortex. Exposure to UVR-B increases p53 and caspase 3 proteins expression just in the lens epithelium. In vivo exposure to subthreshold dose of UVR-B induces apoptosis in the lens epithelial cells and does not in the lens fibre cells.
本研究旨在探究在体内,亚阈值剂量的UVR-B辐射会在晶状体的哪个部位诱导细胞凋亡。
20只6周龄雌性白化Sprague-Dawley大鼠单侧暴露于亚阈值剂量(1kJ/m²)的UVR-B下,并在暴露后120小时处死。摘除晶状体并在三个区域进行解剖:晶状体上皮、皮质和核。然后去除晶状体核。使用凋亡标志物p53和半胱天冬酶3来研究晶状体各区域的细胞凋亡。采用qRT-PCR和蛋白质免疫印迹法分析晶状体。
与未暴露的晶状体相比,暴露的晶状体中,无论是晶状体上皮还是皮质区域,TP53和CASP3 mRNA表达均增加。与未暴露的晶状体上皮相比,暴露的晶状体上皮中p53蛋白表达增加。半胱天冬酶3蛋白在暴露的晶状体上皮细胞中表达,而在未暴露的晶状体上皮细胞中不表达。p53和半胱天冬酶3蛋白在暴露和未暴露的晶状体纤维细胞中均不表达。
暴露于UVR-B会增加体内晶状体两个区域凋亡标志物p53的mRNA转录以及晶状体皮质中凋亡标志物半胱天冬酶3的mRNA转录。暴露于UVR-B仅增加晶状体上皮中p53和半胱天冬酶3蛋白的表达。体内暴露于亚阈值剂量的UVR-B会诱导晶状体上皮细胞凋亡,而不会诱导晶状体纤维细胞凋亡。