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橄榄苦苷增强蛋白酶体活性并降低突变型亨廷顿蛋白诱导的细胞毒性。

Oleuropein enhances proteasomal activity and reduces mutant huntingtin-induced cytotoxicity.

作者信息

Huang Zih-Ning, Lee Sin-Yi, Chen Jie-Mao, Huang Zih-Ting, Her Lu-Shiun

机构信息

Department of Life Sciences, National Cheng Kung University, Tainan, Taiwan.

出版信息

Front Pharmacol. 2024 Sep 13;15:1459909. doi: 10.3389/fphar.2024.1459909. eCollection 2024.

Abstract

INTRODUCTION

Huntington's disease (HD) is a hereditary neurodegenerative disorder that primarily affects the striatum, a brain region responsible for movement control. The disease is characterized by the mutant huntingtin (mHtt) proteins with an extended polyQ stretch, which are prone to aggregation. These mHtt aggregates accumulate in neurons and are the primary cause of the neuropathology associated with HD. To date, no effective cure for HD has been developed.

METHODS

The immortalized ST striatal cell line, the mHtt-transfected wild-type ST striatal cell line, and N2a cells were used as Huntington's disease cell models. Flow cytometry was used to assess cellular reactive oxygen species and transfection efficiency. The CCK-8 assay was used to measure cell viability, while fluorescence microscopy was used to quantify aggregates. Immunoblotting analyses were used to evaluate the effects on protein expression.

RESULTS

Polyphenols are natural antioxidants that offer neuroprotection in neurological disorders. In this study, we provide evidence that oleuropein, the primary polyphenol in olive leaves and olive oil, enhances cell viability in HD cell models, including. ST ST striatal cells, N2a cells ectopically expressing the truncated mHtt, and ST striatal cells expressing the full-length mHtt. Oleuropein effectively reduced both soluble and aggregated forms of mHtt protein in these HD model cells. Notably, the reduction of mHtt aggregates associated with oleuropein was linked to increased proteasome activity rather than changes in autophagic flux. Oleuropein seems to modulate proteasome activity through an unidentified pathway, as it did not affect the 20S proteasome catalytic β subunits, the proteasome regulator PA28γ, or multiple MAPK pathways.

DISCUSSION

We demonstrated that oleuropein enhances the degradation of mHtt by increasing proteasomal protease activities and alleviates mHtt-induced cytotoxicity. Hence, we propose that oleuropein and potentially other polyphenols hold promise as a candidate for alleviating Huntington's disease.

摘要

引言

亨廷顿舞蹈症(HD)是一种遗传性神经退行性疾病,主要影响纹状体,这是一个负责运动控制的脑区。该疾病的特征是突变型亨廷顿蛋白(mHtt)具有延长的多聚谷氨酰胺链,易于聚集。这些mHtt聚集体在神经元中积累,是与HD相关的神经病理学的主要原因。迄今为止,尚未开发出有效的HD治疗方法。

方法

永生化的ST纹状体细胞系、转染了mHtt的野生型ST纹状体细胞系和N2a细胞用作亨廷顿舞蹈症细胞模型。流式细胞术用于评估细胞活性氧和转染效率。CCK-8测定法用于测量细胞活力,而荧光显微镜用于量化聚集体。免疫印迹分析用于评估对蛋白质表达的影响。

结果

多酚是天然抗氧化剂,在神经疾病中具有神经保护作用。在本研究中,我们提供证据表明,橄榄叶和橄榄油中的主要多酚橄榄苦苷可提高HD细胞模型中的细胞活力,包括ST纹状体细胞、异位表达截短型mHtt的N2a细胞以及表达全长mHtt的ST纹状体细胞。橄榄苦苷有效降低了这些HD模型细胞中mHtt蛋白的可溶性和聚集形式。值得注意的是,与橄榄苦苷相关的mHtt聚集体的减少与蛋白酶体活性增加有关,而不是自噬通量的变化。橄榄苦苷似乎通过一条未知途径调节蛋白酶体活性,因为它不影响20S蛋白酶体催化β亚基、蛋白酶体调节剂PA28γ或多个MAPK途径。

讨论

我们证明,橄榄苦苷通过增加蛋白酶体蛋白酶活性来增强mHtt的降解,并减轻mHtt诱导的细胞毒性。因此,我们提出橄榄苦苷以及潜在的其他多酚有望成为缓解亨廷顿舞蹈症的候选物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9aed/11440197/e2c401cb4842/fphar-15-1459909-g001.jpg

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