EGCG通过PAK1/Cleaved Caspase-3通路减轻年龄相关性白内障晶状体上皮细胞凋亡

IF 2.2 4区 医学 Q3 MEDICINE, RESEARCH & EXPERIMENTAL
Yue Zhang, Dongmei Su, Zhaoyi Sun, Yanjiang Fu, Xiaoya Chen, Yuzhu Hu, Xiao Zhang, Shunfei Zheng, Xu Ma, Shanshan Hu
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引用次数: 0

摘要

背景:晶状体上皮细胞(LECs)的氧化损伤和凋亡是导致年龄相关性白内障(ARC)发生的主要因素。表没食子儿茶素没食子酸酯(EGCG)对lec的潜在保护作用尚不清楚,尽管其具有显著的抗氧化和抗凋亡特性。本研究的目的是探讨丝氨酸/苏氨酸蛋白激酶(PAK1)在egcg介导的h2o2诱导的LECs细胞凋亡的体内和体外抑制中的作用。方法:采用western blotting和免疫组化方法检测小鼠和非ARC患者晶状体前囊中PAK1的表达。采用EGCG+H2O2或仅H2O2预处理人晶状体上皮细胞B3 (hl -B3),采用qRT-PCR和western blotting检测PAK1的表达。细胞凋亡(PAK1过表达或沉默后)和细胞存活分别采用Hoechst 33342染色和细胞计数Kit-8测定。通过western blotting在横切细胞、老年/年轻小鼠和EGCG处理小鼠中检测裂解的caspase-3。结果:PAK1在ARC LECs中的表达明显低于对照LECs。在hl - b3细胞中,EGCG+H2O2处理与单独H2O2处理相比,上调了PAK1 mRNA和蛋白的表达。PAK1过表达可减轻H2O2诱导的LECs细胞凋亡,而低表达可减弱EGCG的保护作用。PAK1过表达降低了h2o2处理细胞中cleaved caspase-3的表达,而PAK1沉默增加了EGCG+ h2o2处理细胞中caspase-3的表达。EGCG降低h2o2处理细胞中cleaved caspase-3的表达。这些结果表明PAK1抑制裂解的caspase-3表达,从而增强EGCG对h2o2诱导的LEC凋亡的抑制作用。结论:PAK1/cleaved caspase-3通路在EGCG对ARC发生的保护作用中起关键作用。这为EGCG预防和治疗ARC提供了新的治疗靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
EGCG Mitigates Apoptosis of Lens Epithelial Cells in Age-Related Cataract via the PAK1/Cleaved Caspase-3 Pathway.

Background: Oxidative damage and apoptosis of lens epithelial cells (LECs) are the primary factors contributing to the development of age-related cataracts (ARC). The potential protective effects of epigallocatechin gallate (EGCG) on LECs remain unclear despite its remarkable antioxidant and anti-apoptotic properties. The aim of this study was to explore the role of serine/threonine-protein kinase (PAK1) in EGCG-mediated attenuation of H2O2-induced apoptosis of LECs in vivo and in vitro.

Methods: PAK1 expression was assessed in the anterior capsule of the lens from mice and patients with and without ARC using western blotting and immunohistochemistry. Human lens epithelial B3 (HLE-B3) cells were pre-treated with EGCG+H2O2 or H2O2 only, and PAK1 expression was determined using qRT-PCR and western blotting. Apoptosis (following PAK1 overexpression or silencing) and cell survival were assessed using Hoechst 33342 staining and a cell counting Kit-8 assay, respectively. Cleaved caspase-3 was measured in transected cells, aged/young mice, and mice treated with EGCG via western blotting.

Results: PAK1 expression was significantly lower in ARC LECs than in control LECs. In HLE-B3 cells, EGCG+H2O2 treatment upregulated PAK1 mRNA and protein expression when compared with H2O2 alone. PAK1 overexpression alleviated H2O2- induced apoptosis in LECs, while low expression weakened EGCG's protective effects. PAK1 overexpression reduced cleaved caspase-3 expression in H2O2-treated cells, whereas PAK1 silencing increased its expression in EGCG+H2O2-treated cells. EGCG decreased cleaved caspase-3 expression in H2O2-treated cells. These results suggest that PAK1 inhibits cleaved caspase-3 expression, thereby enhancing EGCG's attenuation of H2O2-induced LEC apoptosis.

Conclusion: The PAK1/cleaved caspase-3 pathway plays a key role in EGCG's protective effects on the development of ARC. This provides a new therapeutic target for the use of EGCG in preventing and treating ARC.

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来源期刊
Current molecular medicine
Current molecular medicine 医学-医学:研究与实验
CiteScore
5.00
自引率
4.00%
发文量
141
审稿时长
4-8 weeks
期刊介绍: Current Molecular Medicine is an interdisciplinary journal focused on providing the readership with current and comprehensive reviews/ mini-reviews, original research articles, short communications/letters and drug clinical trial studies on fundamental molecular mechanisms of disease pathogenesis, the development of molecular-diagnosis and/or novel approaches to rational treatment. The reviews should be of significant interest to basic researchers and clinical investigators in molecular medicine. Periodically the journal invites guest editors to devote an issue on a basic research area that shows promise to advance our understanding of the molecular mechanism(s) of a disease or has potential for clinical applications.
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