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杆状光感受器中的自噬由光转导和错误折叠的 RHO 独立调节。

Autophagy in rod photoreceptors is independently regulated by phototransduction and misfolded RHO.

机构信息

Department of Ophthalmology and Visual Sciences, University of British Columbia , Vancouver , British Columbia , Canada.

出版信息

Autophagy. 2019 Nov;15(11):1970-1989. doi: 10.1080/15548627.2019.1596487. Epub 2019 Apr 12.

Abstract

We previously reported autophagic structures in rod photoreceptors expressing a misfolding RHO (rhodopsin) mutant (RHO), suggesting that autophagy may play a role in degrading the mutant RHO and/or be involved in photoreceptor cell death. To further examine autophagy in normal and diseased rods, we generated transgenic tadpoles expressing the dually fluorescent autophagy marker mRFP-eGFP-LC3 in rods, which changes from green to yellow and finally red as autophagic structures develop and mature. Using transgenic lines with constitutive and inducible expression, we determined the time-course of autophagy in rod photoreceptors: autophagosomes last for 6 to 8 hours before fusing with lysosomes, and acidified autolysosomes last for about 28 hours before being degraded. Autophagy was diurnally regulated in normal rods, with more autophagic structures generated during periods of light, and this regulation was non-circadian. We also found that more autophagosomes were produced in rods expressing the misfolding RHO mutant. The RHO chromophore absorbs photons to initiate phototransduction, and is consumed in this process; it also promotes RHO folding. To determine whether increased autophagy in light-exposed normal rods is caused by increased RHO misfolding or phototransduction, we used CRISPR/Cas9 to knock out the and genes, which are essential for chromophore biosynthesis and phototransduction respectively. Both knockouts suppressed light-induced autophagy, indicating that although light and misfolded rhodopsin can both induce autophagy in rods, light-induced autophagy is not due to misfolding of RHO, but rather due to phototransduction. : CYCS: cytochrome c; bRHO: bovine RHO; Cas9: CRISPR associated protein 9; dpf: days post-fertilization; eGFP: enhanced green fluorescent protein; GNAT1: guanine nucleotide-binding protein G(t) subunit alpha-1 aka rod alpha-transducin; HSPA1A/hsp70: heat shock protein of 70 kilodaltons; LAMP1: lysosomal-associated membrane protein 1; LC3: microtubule-associated protein 1A/1B light chain 3; mRFP: monomeric red fluorescent protein; RHO: rhodopsin; RP: retinitis pigmentosa; RPE65: retinal pigment epithelium-specific 65 kDa protein: sfGFP: superfolding GFP; sgRNA: single guide RNA; WGA: wheat germ agglutinin; : the promoter.

摘要

我们之前曾报道过在表达错误折叠 RHO(视紫红质)突变体(RHO)的杆状光感受器中存在自噬结构,这表明自噬可能在降解突变型 RHO 中发挥作用,或者参与光感受器细胞死亡。为了进一步研究正常和患病的杆状细胞中的自噬作用,我们在杆状细胞中生成了表达双重荧光自噬标记物 mRFP-eGFP-LC3 的转基因 蝌蚪,该标记物在自噬体发育和成熟过程中会从绿色变为黄色,最终变为红色。使用具有组成型和诱导型表达的转基因系,我们确定了杆状光感受器中自噬的时程:自噬体在与溶酶体融合之前持续 6 到 8 小时,而酸化的自噬溶酶体在被降解之前持续约 28 小时。正常杆状细胞中的自噬作用呈昼夜节律调节,在光照期间会产生更多的自噬体,这种调节是非昼夜节律的。我们还发现,在表达错误折叠 RHO 突变体的杆状细胞中产生了更多的自噬体。RHO 色素吸收光子以启动光转导,在此过程中被消耗;它还促进 RHO 折叠。为了确定在光照下的正常杆状细胞中增加的自噬是否是由 RHO 错误折叠或光转导增加引起的,我们使用 CRISPR/Cas9 敲除了 和 基因,这两个基因分别是色素生物合成和光转导所必需的。两个敲除均抑制了光诱导的自噬,表明尽管光和错误折叠的视紫红质都可以在杆状细胞中诱导自噬,但光诱导的自噬不是由于 RHO 的错误折叠引起的,而是由于光转导引起的。 CYCS:细胞色素 c;bRHO:牛视紫红质;Cas9:CRISPR 相关蛋白 9;dpf:受精后天数;eGFP:增强型绿色荧光蛋白;GNAT1:鸟嘌呤核苷酸结合蛋白 G(t)亚基α-1,又名 rod alpha-转导蛋白;HSPA1A/hsp70:热休克蛋白 70 千道尔顿;LAMP1:溶酶体相关膜蛋白 1;LC3:微管相关蛋白 1A/1B 轻链 3;mRFP:单体红色荧光蛋白;RHO:视紫红质;RP:色素性视网膜炎;RPE65:视网膜色素上皮特异性 65 kDa 蛋白;sfGFP:超折叠 GFP;sgRNA:单指导 RNA;WGA:麦胚凝集素;:启动子。

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