Department of Human Anatomy, Histology and Embryology, School of Basic Medicine, Qingdao University, Qingdao, China.
The 971 Hospital of the Chinese People's Liberation Army Navy, Qingdao, China.
J Cell Mol Med. 2023 Mar;27(6):803-818. doi: 10.1111/jcmm.17679. Epub 2023 Feb 23.
The lens is transparent, non-vascular, elastic and wrapped in a transparent capsule. The lens oppacity of AQP5 mice was increased more than that of wild-type (AQP5 ) mice. In this study, we explored the potential functional role of circular RNAs (circRNAs) and transcription factor HSF4 in lens opacity in aquaporin 5 (AQP5) knockout (AQP5 ) mice. Autophagy was impaired in the lens tissues of AQP5 mice. Autophagic lysosomes in lens epithelial cells of AQP5 mice were increased compared with AQP5 mice, based on analysis by transmission electron microscopy. The genetic information of the mice lens was obtained by high-throughput sequencing, and then the downstream genes were analysed. A circRNA-miRNA-mRNA network related to lysosomal pathway was constructed by the bioinformatics analysis of the differentially expressed circRNAs. Based on the prediction of the TargetScan website and the validation by dual luciferase reporter assay and RNA immunoprecipitation-qPCR, we found that circRNA (Chr16: 33421321-33468183+) inhibited the function of HSF4 by sponging microRNA (miR-149-5p), and it downregulated the normal expression of lysosome-related mRNAs. The accumulation of autophagic lysosome may be one of the reasons for the abnormal development of the lens in AQP5 mice.
晶状体透明、无血管、有弹性,被一层透明囊包裹。AQP5 敲除(AQP5-/-)小鼠的晶状体不透明度增加超过野生型(WT)小鼠。在这项研究中,我们探索了环状 RNA(circRNA)和转录因子 HSF4 在水通道蛋白 5(AQP5)敲除(AQP5-/-)小鼠晶状体混浊中的潜在功能作用。AQP5 敲除(AQP5-/-)小鼠的晶状体组织中自噬受损。透射电子显微镜分析显示,AQP5 敲除(AQP5-/-)小鼠的晶状体上皮细胞中的自噬溶酶体增加。通过高通量测序获得小鼠晶状体的遗传信息,然后分析下游基因。通过对差异表达的 circRNAs 的生物信息学分析,构建了与溶酶体途径相关的 circRNA-miRNA-mRNA 网络。通过 TargetScan 网站的预测和双荧光素酶报告基因检测及 RNA 免疫沉淀-qPCR 的验证,我们发现 circRNA(Chr16:33421321-33468183+)通过海绵 microRNA(miR-149-5p)抑制 HSF4 的功能,下调了溶酶体相关 mRNA 的正常表达。自噬溶酶体的积累可能是 AQP5 敲除(AQP5-/-)小鼠晶状体异常发育的原因之一。