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选择性丧失 RPGRIP1 依赖性的 NPHP4、RPGR 和 SDCCAG8 纤毛靶向导致光感受器神经元变性。

Selective loss of RPGRIP1-dependent ciliary targeting of NPHP4, RPGR and SDCCAG8 underlies the degeneration of photoreceptor neurons.

机构信息

Department of Ophthalmology, Duke University Medical Center, Durham, NC, USA.

出版信息

Cell Death Dis. 2012 Jul 19;3(7):e355. doi: 10.1038/cddis.2012.96.

Abstract

The retinitis pigmentosa GTPase regulator (RPGR) and nephrocystin-4 (NPHP4) comprise two key partners of the assembly complex of the RPGR-interacting protein 1 (RPGRIP1). Mutations in RPGR and NPHP4 are linked to severe multisystemic diseases with strong retinal involvement of photoreceptor neurons, whereas those in RPGRIP1 cause the fulminant photoreceptor dystrophy, Leber congenital amaurosis (LCA). Further, mutations in Rpgrip1 and Nphp4 suppress the elaboration of the outer segment compartment of photoreceptor neurons by elusive mechanisms, the understanding of which has critical implications in uncovering the pathogenesis of syndromic retinal dystrophies. Here we show RPGRIP1 localizes to the photoreceptor connecting cilium (CC) distally to the centriole/basal body marker, centrin-2 and the ciliary marker, acetylated-α-tubulin. NPHP4 abuts proximally RPGRIP1, RPGR and the serologically defined colon cancer antigen-8 (SDCCAG8), a protein thought to partake in the RPGRIP1 interactome and implicated also in retinal-renal ciliopathies. Ultrastructurally, RPGRIP1 localizes exclusively throughout the photoreceptor CC and Rpgrip1(nmf247) photoreceptors present shorter cilia with a ruffled membrane. Strikingly, Rpgrip1(nmf247) mice without RPGRIP1 expression lack NPHP4 and RPGR in photoreceptor cilia, whereas the SDCCAG8 and acetylated-α-tubulin ciliary localizations are strongly decreased, even though the NPHP4 and SDCCAG8 expression levels are unaffected and those of acetylated-α-tubulin and γ-tubulin are upregulated. Further, RPGRIP1 loss in photoreceptors shifts the subcellular partitioning of SDCCAG8 and NPHP4 to the membrane fraction associated to the endoplasmic reticulum. Conversely, the ciliary localization of these proteins is unaffected in glomeruli or tubular kidney cells of Rpgrip1(nmf247), but NPHP4 is downregulated developmentally and selectively in kidney cortex. Hence, RPGRIP1 presents cell type-dependent pathological effects crucial to the ciliary targeting and subcellular partitioning of NPHP4, RPGR and SDCCAG8, and acetylation of ciliary α-tubulin or its ciliary targeting, selectively in photoreceptors, but not kidney cells, and these pathological effects underlie photoreceptor degeneration and LCA.

摘要

色素性视网膜炎 GTP 酶调节因子 (RPGR) 和多囊肾病蛋白-4 (NPHP4) 是 RPGR 相互作用蛋白 1 (RPGRIP1) 组装复合物的两个关键伴侣。RPGR 和 NPHP4 的突变与严重的多系统疾病有关,这些疾病强烈涉及感光神经元的视网膜,而 RPGRIP1 的突变导致暴发性感光细胞营养不良,莱伯先天性黑蒙 (LCA)。此外,Rpgrip1 和 Nphp4 的突变通过难以捉摸的机制抑制感光神经元外节室的形成,了解这些机制对揭示综合征性视网膜营养不良的发病机制具有重要意义。在这里,我们显示 RPGRIP1 定位于远心的感光细胞连接纤毛 (CC),靠近中心粒/基底体标记物 centrin-2 和纤毛标记物乙酰化-α-微管蛋白。NPHP4 靠近 RPGRIP1、RPGR 和血清学定义的结肠癌抗原-8 (SDCCAG8),后者被认为参与 RPGRIP1 相互作用组,也与视网膜-肾纤毛病变有关。超微结构显示,RPGRIP1 仅在整个感光细胞 CC 中定位,而 Rpgrip1(nmf247)感光细胞的纤毛较短,膜起皱。引人注目的是,缺乏 RPGRIP1 表达的 Rpgrip1(nmf247)小鼠在感光细胞纤毛中缺乏 NPHP4 和 RPGR,而 SDCCAG8 和乙酰化-α-微管蛋白纤毛定位强烈减少,尽管 NPHP4 和 SDCCAG8 的表达水平不受影响,而乙酰化-α-微管蛋白和 γ-微管蛋白的表达水平上调。此外,感光细胞中 RPGRIP1 的缺失将 SDCCAG8 和 NPHP4 的亚细胞分布转移到与内质网相关的膜部分。相反,在 Rpgrip1(nmf247)的肾小球或肾小管肾细胞中,这些蛋白质的纤毛定位不受影响,但 NPHP4 在发育过程中选择性地下调,并在肾脏皮质中选择性地下调。因此,RPGRIP1 表现出对 NPHP4、RPGR 和 SDCCAG8 的纤毛靶向和亚细胞分布以及对纤毛 α-微管蛋白的乙酰化或其纤毛靶向至关重要的细胞类型依赖性病理效应,选择性地在感光细胞中,而不是在肾细胞中,这些病理效应是感光细胞变性和 LCA 的基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c1a/3406595/740d6606c196/cddis201296f1.jpg

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