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首页> 外文期刊>Experimental Eye Research >Age-related distribution and potential role of SNCB in topographically different retinal areas of the common marmoset Callithrix jacchus, including the macula
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Age-related distribution and potential role of SNCB in topographically different retinal areas of the common marmoset Callithrix jacchus, including the macula

机译:与普通Marmoset Callithrix Jacchus的平息不同视网膜区域的年龄相关的分布和SNCB的潜在作用,包括黄斑

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摘要

Evidence of an age-related increase of beta-synuclein (SNCB) in several parts of the visual system including the retina has been reported. SNCB is thought to function as an antagonist of alpha-synuclein in neurodegenerative diseases, but the exact role of SNCB remains unclear. The presented work studies two different aspects of the onset and role of SNCB in the retinal pigment epithelium (RPE). First, the topographical and intracellular distributions of SNCB in the RPE of non-human marmoset monkey (Callithrix jacchus) were evaluated in paraffin-embedded eyes and RPE whole mounts from different developmental stages (neonatal, adolescent, and adult). Thus, revealed distinct lifetime-related alterations of the topographical and intracellular distributions of SNCB in the primate macula compared to the retinal periphery. Furthermore, the function and influences of SNCB on ARPE-19 cells and primary porcine RPE (ppRPE) cells were characterized by exposing these cells with recombinant SNCB (rSNCB) at different concentrations. Moreover, apoptosis, protein- and mRNA-expression levels of factors of the p53/MDM2 signaling cascade and inflammation- and oxidation-related genes were investigated. The observed dose-depended decreased apoptosis rates together with the PLD2 mediated activation of the p53 pathway promotes senescence-related processes in SNCB exposed common ARPE-19 cells from human origin. Further, increased HMOX1 and NOX4 levels indicate increased oxidative stress and inflammatory responses triggered by SNCB. The obtained differences in the distribution of SNCB in primate RPE together with alterations of cellular functions in rSNCB-exposed RPE cells (e.g., ARPE-19, ppRPE) support SNCB-related effects like inflammatory response and stress-related properties on RPE over lifetime. The possible functional relevance of SNCB in physiological aging converting into a pathophysiological condition should be investigated in further studies.
机译:据报道,β-突触核蛋白(SNCB)在包括视网膜的若干部分中β-突触核蛋白(SNCB)的验证的证据。 SNCB被认为用作神经变性疾病中α-突触核蛋白的拮抗剂,但SNCB的确切作用尚不清楚。所呈现的工作研究了视网膜颜料上皮(RPE)中SNCB的发作和作用的两种不同方面。首先,在石蜡包埋的眼睛和来自不同发育阶段的石蜡嵌入式眼睛和RPE的全部安装段(新生儿,青少年和成人)中评估SNCB的地形和细胞内分布。因此,与视网膜周边相比,揭示了与视网膜脉冲中灵长类动物的平面和细胞内分布的不同寿命相关的改变。此外,通过在不同浓度下将具有重组SNCB(RSNCB)暴露于不同浓度的细胞,表征SNCB对ARPE-19细胞和初级猪RPE(PPRPE)细胞的功能和影响。此外,研究了P53 / MDM2信号传导级联和炎症和氧化相关基因的凋亡,蛋白质和mRNA表达水平和炎症和氧化相关基因。观察到的剂量依赖于凋亡率降低以及PLD2介导的P53途径的活化促进了SNCB中的衰老相关方法,暴露于人来源的常见ArPe-19细胞。此外,增加的HMOX1和NOX4水平表明SNCB引发的氧化应激和炎症反应增加。获得灵长类动物RPE中SNCB分布的差异以及RSNCB暴露的RPE细胞中细胞功能的改变(例如,ARPE-19,PPRPE)支持SNCB相关的效果,如炎症反应和RPE上的应力相关性能。在进一步的研究中,应研究SNCB在生理老化中转化为病理生理病症的可能功能性相关性。

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