Neurobiology-Neurodegeneration & Repair Laboratory, National Eye Institute, National Institutes of Health, Bethesda, MD 20892, USA.
Imaging Core, National Eye Institute, National Institutes of Health, Bethesda, MD 20892, USA.
Hum Mol Genet. 2018 Oct 15;27(20):3555-3567. doi: 10.1093/hmg/ddy272.
In the mammalian retina, rod and cone photoreceptors transmit the visual information to bipolar neurons through highly specialized ribbon synapses. We have limited understanding of regulatory pathways that guide morphogenesis and organization of photoreceptor presynaptic architecture in the developing retina. While neural retina leucine zipper (NRL) transcription factor determines rod cell fate and function, cone-rod homeobox (CRX) controls the expression of both rod- and cone-specific genes and is critical for terminal differentiation of photoreceptors. A comprehensive immunohistochemical evaluation of Crx-/- (null), CrxRip/+ and CrxRip/Rip (models of dominant congenital blindness) mouse retinas revealed abnormal photoreceptor synapses, with atypical ribbon shape, number and length. Integrated analysis of retinal transcriptomes of Crx-mutants with CRX- and NRL-ChIP-Seq data identified a subset of differentially expressed CRX target genes that encode presynaptic proteins associated with the cytomatrix active zone (CAZ) and synaptic vesicles. Immunohistochemistry of Crx-mutant retina validated aberrant expression of REEP6, PSD95, MPP4, UNC119, UNC13, RGS7 and RGS11, with some reduction in Ribeye and no significant change in immunostaining of RIMS1, RIMS2, Bassoon and Pikachurin. Our studies demonstrate that CRX controls the establishment of CAZ and anchoring of ribbons, but not the formation of ribbon itself, in photoreceptor presynaptic terminals.
在哺乳动物的视网膜中,视杆细胞和视锥细胞通过高度特化的带状突触将视觉信息传递给双极神经元。我们对指导发育中视网膜中光感受器前突触结构的形态发生和组织的调节途径知之甚少。虽然神经视网膜亮氨酸拉链(NRL)转录因子决定了视杆细胞的命运和功能,但 cone-rod homeobox(CRX)控制着 rod- 和 cone-特异性基因的表达,对于光感受器的终末分化至关重要。对 Crx-/-(null)、CrxRip/+ 和 CrxRip/Rip(显性先天性失明模型)小鼠视网膜的全面免疫组织化学评估显示,异常的光感受器突触具有非典型的带状形状、数量和长度。Crx 突变体的视网膜转录组与 CRX 和 NRL-ChIP-Seq 数据的综合分析确定了一组差异表达的 CRX 靶基因,这些基因编码与细胞基质活性区(CAZ)和突触小泡相关的突触前蛋白。Crx 突变体视网膜的免疫组织化学验证了 REEP6、PSD95、MPP4、UNC119、UNC13、RGS7 和 RGS11 的异常表达,其中 Ribeye 减少,而 RIMS1、RIMS2、Bassoon 和 Pikachurin 的免疫染色没有明显变化。我们的研究表明,CRX 控制 CAZ 的建立和带状物的锚定,但不控制光感受器前突触末端中带状物本身的形成。