Li Y, Zhang F, Lu W, Li X
The State Key Laboratory of Ophthalmology, Zhongshan Ophthalmic Center, Sun Yat-sen University, Guangzhou 510060, China.
Laboratory of Molecular Genetics, National Heart, Lung, and Blood Institute, NIH, Bethesda, MD 20824, United States.
Curr Mol Med. 2018 Mar 9;17(7):497-508. doi: 10.2174/1566524018666180212144500.
Photoreceptor cell death is a key pathology of retinal degeneration diseases. To date, the molecular mechanisms for this pathological process remain largely unclear. Junctional adhesion molecule-c (Jam-c) has been shown to play important roles in different biological events. However, its effect on retinal neuronal cells is unknown.
To determine the effect of Jam-c on adult mouse eyes, particularly, on retinal structure, vasculature and photoreceptor cells, in order to explore potential important target molecules for ocular diseases.
Jam-c global knockout mice, endothelial-specific and neuronal-specific Jam-c conditional knockout mice using Tie2-Cre and Nestin-Cre mice respectively were used in this study. Mouse eyes were harvested from the different groups and eye size examined. Cryosections of the eyes were made and stained with Hematoxylin and Eosin (H&E) and the thicknesses of retinal layers measured. Retinal blood vessels and cone and rod photoreceptors were analyzed using isolectin B4, peanut agglutinin and rhodopsin as markers respectively. In vivo Jam-c knockdown in mouse eyes was performed by intravitreal injection of Jam-c shRNA. Jam-c expression in the retinae was quantified by real-time PCR.
Global Jam-c gene deletion in mice resulted in smaller eyes and decreased the diameters of lens and iris. Jam-c-/- mice display marked thinning of the outer nuclear layer (ONL), less numbers of photoreceptor cells, and abnormal retinal vasculature. Importantly, neuronal-specific Jam-c deletion led to similar phenotype, whereas no obvious defect was observed in endothelial-specific Jam-c knockout mice. Moreover, Jam-c knockdown by shRNA also decreased ONL thickness and photoreceptor numbers.
We found that Jam-c is critically required for the normal size and retinal structure. Particularly, Jam-c plays important roles in maintaining the normal retinal thickness, vasculature and photoreceptor numbers. Jam-c thus may therefore have important roles in various ocular diseases.
光感受器细胞死亡是视网膜变性疾病的关键病理特征。迄今为止,这一病理过程的分子机制仍不清楚。连接黏附分子c(Jam-c)已被证明在不同的生物学事件中发挥重要作用。然而,其对视网膜神经细胞的影响尚不清楚。
确定Jam-c对成年小鼠眼睛的影响,特别是对视网膜结构、血管系统和光感受器细胞的影响,以探索眼部疾病潜在的重要靶分子。
本研究使用了Jam-c全基因敲除小鼠、分别利用Tie2-Cre和Nestin-Cre小鼠构建的内皮细胞特异性和神经元特异性Jam-c条件性敲除小鼠。从不同组中采集小鼠眼睛并检查眼睛大小。制作眼睛的冰冻切片,用苏木精和伊红(H&E)染色,并测量视网膜各层的厚度。分别使用异凝集素B4、花生凝集素和视紫红质作为标记物分析视网膜血管以及视锥和视杆光感受器。通过玻璃体内注射Jam-c shRNA在小鼠眼中进行体内Jam-c基因敲低。通过实时PCR定量视网膜中Jam-c的表达。
小鼠中Jam-c基因的整体缺失导致眼睛变小,晶状体和虹膜直径减小。Jam-c-/-小鼠的外核层(ONL)明显变薄,光感受器细胞数量减少,视网膜血管系统异常。重要的是,神经元特异性Jam-c缺失导致了类似的表型,而在内皮细胞特异性Jam-c敲除小鼠中未观察到明显缺陷。此外,shRNA介导的Jam-c基因敲低也降低了ONL厚度和光感受器数量。
我们发现Jam-c对于正常的眼睛大小和视网膜结构至关重要。特别是,Jam-c在维持正常的视网膜厚度、血管系统和光感受器数量方面发挥重要作用。因此,Jam-c可能在各种眼部疾病中发挥重要作用。