Chung Yin-Sir, Ahmed Pervaiz Khalid, Othman Iekhsan, Shaikh Mohd Farooq
Neuropharmacology Research Laboratory, Jeffrey Cheah School of Medicine and Health Sciences, Monash University Malaysia, Bandar Sunway 47500, Malaysia.
School of Business, Monash University Malaysia, Bandar Sunway 47500, Malaysia.
Life (Basel). 2021 Jun 20;11(6):585. doi: 10.3390/life11060585.
The neuroprotective potential of leaf proteins (OSLPs) has never been evaluated in SH-SY5Y cells challenged by hydrogen peroxide (HO). This work thus aims to elucidate OSLP neuroprotective potential in alleviating HO stress. OSLPs at varying concentrations were evaluated for cytotoxicity (24 and 48 h) and neuroprotective potential in HO-induced SH-SY5Y cells (24 h). The protective mechanism of HO-induced SH-SY5Y cells was also explored via mass-spectrometry-based label-free quantitative proteomics (LFQ) and bioinformatics. OSLPs (25, 50, 125, 250, 500, and 1000 µg/mL; 24 and 48 h) were found to be safe. Pre-treatments with OSLP doses (250, 500, and 1000 µg/mL, 24 h) significantly increased the survival of SH-SY5Y cells in a concentration-dependent manner and improved cell architecture-pyramidal-shaped cells, reduced clumping and shrinkage, with apparent neurite formations. OSLP pre-treatment (1000 µg/mL, 24 h) lowered the expressions of two major heat shock proteins, HSPA8 (heat shock protein family A (Hsp70) member 8) and HSP90AA1 (heat shock protein 90), which promote cellular stress signaling under stress conditions. OSLP is, therefore, suggested to be anti-inflammatory by modulating the "signaling of interleukin-4 and interleukin-13" pathway as the predominant mechanism in addition to regulating the "attenuation phase" and "HSP90 chaperone cycle for steroid hormone receptors" pathways to counteract heat shock protein (HSP)-induced damage under stress conditions.
叶蛋白(OSLPs)的神经保护潜力从未在受到过氧化氢(HO)攻击的SH-SY5Y细胞中得到评估。因此,这项工作旨在阐明OSLPs在减轻HO应激方面的神经保护潜力。评估了不同浓度的OSLPs在HO诱导的SH-SY5Y细胞中的细胞毒性(24和48小时)和神经保护潜力(24小时)。还通过基于质谱的无标记定量蛋白质组学(LFQ)和生物信息学探索了HO诱导的SH-SY5Y细胞的保护机制。发现OSLPs(25、50、125、250、500和1000μg/mL;24和48小时)是安全的。用OSLP剂量(250、500和1000μg/mL,24小时)预处理以浓度依赖性方式显著提高了SH-SY5Y细胞的存活率,并改善了细胞结构——呈金字塔形细胞,减少了聚集和收缩,有明显的神经突形成。OSLP预处理(1000μg/mL,24小时)降低了两种主要热休克蛋白HSPA8(热休克蛋白家族A(Hsp70)成员8)和HSP90AA1(热休克蛋白90)的表达,这两种蛋白在应激条件下促进细胞应激信号传导。因此,除了调节“衰减期”和“类固醇激素受体的HSP90伴侣循环”途径以抵消应激条件下热休克蛋白(HSP)诱导的损伤外,OSLP还被认为通过调节“白细胞介素-4和白细胞介素-13信号传导”途径作为主要机制具有抗炎作用。