Yu Shanshan, Li Chang, Biswas Lincoln, Hu Xuebin, Liu Fei, Reilly James, Liu Xiliang, Liu Ying, Huang Yuwen, Lu Zhaojing, Han Shanshan, Wang Lei, Yu Liu Jing, Jiang Tao, Shu Xinhua, Wong Fulton, Tang Zhaohui, Liu Mugen
Key Laboratory of Molecular Biophysics of Ministry of Education, Department of Genetics and Developmental Biology, College of Life Science and Technology, Huazhong University of Science and Technology, Wuhan, Hubei 430074, P.R. China.
Department of Life Sciences, Glasgow Caledonian University, Glasgow G4?0BA, UK.
Hum Mol Genet. 2017 Jun 15;26(12):2335-2345. doi: 10.1093/hmg/ddx137.
In humans, CERKL mutations cause widespread retinal degeneration: early dysfunction and loss of rod and cone photoreceptors in the outer retina and, progressively, death of cells in the inner retina. Despite intensive efforts, the function of CERKL remains obscure and studies in animal models have failed to clarify the disease mechanism of CERKL mutations. To address this gap in knowledge, we have generated a stable CERKL knockout zebrafish model by TALEN technology and a 7bp deletion in CERKL cDNA that caused the premature termination of CERKL. These CERKL-/- animals showed progressive degeneration of photoreceptor outer segments (OSs) and increased apoptosis of retinal cells, including those in the outer and inner retinal layers. Additionally, we confirmed by immunofluorescence and western-blot that rod degeneration in CERKL-/- zebrafish occurred earlier and was more significant than that in cone cells. Accumulation of shed OSs in the interphotoreceptor matrix was observed by transmission election microscopy (TEM). This suggested that CERKL may regulate the phagocytosis of OSs by the retinal pigment epithelium (RPE). We further found that the phagocytosis-associated protein MERTK was significantly reduced in CERKL-/- zebrafish. Additionally, in ARPE-19 cell lines, knockdown of CERKL also decreased the mRNA and protein level of MERTK, as well as the ox-POS phagocytosis. We conclude that CERKL deficiency in zebrafish may cause rod-cone dystrophy, but not cone-rod dystrophy, while interfering with the phagocytosis function of RPE associated with down-regulation of the expression of MERTK.
在人类中,CERKL突变会导致广泛的视网膜变性:外视网膜中的视杆和视锥光感受器早期功能障碍并丧失,随后,内视网膜中的细胞逐渐死亡。尽管付出了巨大努力,CERKL的功能仍然不清楚,动物模型研究也未能阐明CERKL突变的疾病机制。为了填补这一知识空白,我们利用TALEN技术构建了一个稳定的CERKL基因敲除斑马鱼模型,并在CERKL cDNA中产生了一个7bp的缺失,导致CERKL过早终止。这些CERKL-/-动物表现出光感受器外段(OS)的进行性退化以及视网膜细胞凋亡增加,包括外视网膜层和内视网膜层的细胞。此外,我们通过免疫荧光和蛋白质印迹证实,CERKL-/-斑马鱼中的视杆退化比视锥细胞更早且更显著。通过透射电子显微镜(TEM)观察到光感受器间基质中脱落的OS堆积。这表明CERKL可能调节视网膜色素上皮(RPE)对OS的吞噬作用。我们进一步发现,CERKL-/-斑马鱼中与吞噬作用相关的蛋白MERTK显著减少。此外,在ARPE-19细胞系中,敲低CERKL也降低了MERTK的mRNA和蛋白水平以及氧化型光感受器外段(ox-POS)的吞噬作用。我们得出结论,斑马鱼中CERKL缺乏可能导致视杆-视锥营养不良,但不会导致视锥-视杆营养不良,同时会干扰与MERTK表达下调相关的RPE吞噬功能。