School of Environmental Science and Engineering, Shandong University, China-America CRC for Environment & Health, 72# Jimo Binhai Road, Qingdao, Shandong 266237, PR China.
School of Chemistry and Chemical Engineering, Qilu University of Technology (Shandong Academy of Sciences), Jinan 250353, PR China.
J Hazard Mater. 2024 Mar 5;465:133032. doi: 10.1016/j.jhazmat.2023.133032. Epub 2023 Nov 22.
Nanoplastics (NPs) are currently everywhere and environmental pollution by NPs is a pressing global problem. Nevertheless, until now, few studies have concentrated on the mechanisms and pathways of cytotoxic effects and immune dysfunction of NPs on soil organisms employing a multidimensional strategy. Hence, earthworm immune cells and immunity protein lysozyme (LZM) were selected as specific receptors to uncover the underlying mechanisms of cytotoxicity, genotoxicity, and immunotoxicity resulting from exposure to polystyrene nanoplastics (PS-NPs), and the binding mechanisms of PS-NPs-LZM interaction. Results on cells indicated that when earthworm immune cells were exposed to high-dose PS-NPs, it caused a notable rise in the release of reactive oxygen species (ROS), resulting in oxidative stress. PS-NPs exposure significantly decreased the cell viability of earthworm immune cells, inducing cytotoxicity through ROS-mediated oxidative stress pathway, and oxidative injury effects, including reduced antioxidant defenses, lipid peroxidation, DNA damage, and protein oxidation. Moreover, PS-NPs stress inhibited the intracellular LZM activity in immune cells, resulting in impaired immune function and immunotoxicity by activating the oxidative stress pathway mediated by ROS. The results from molecular studies revealed that PS-NPs binding destroyed the LZM structure and conformation, including secondary structure changes, protein skeleton unfolding/loosening, fluorescence sensitization, microenvironment changes, and particle size changes. Molecular docking suggested that PS-NPs combined with active center of LZM easier and inhibited the protein function more, and formed a hydrophobic interaction with TRP 62, a crucial amino acid residue closely associated with the function and conformation of LZM. This is also responsible for LZM conformational changes and functional inhibition /inactivation. These results of this research offer a fresh outlook on evaluating the detriment of NPs to the immune function of soil organisms using cellular and molecular strategies.
纳米塑料(NPs)无处不在,纳米塑料造成的环境污染是一个紧迫的全球性问题。然而,到目前为止,很少有研究采用多维策略集中研究纳米塑料对土壤生物的细胞毒性作用和免疫功能障碍的机制和途径。因此,选择蚯蚓免疫细胞和免疫蛋白溶菌酶(LZM)作为特定受体,以揭示暴露于聚苯乙烯纳米塑料(PS-NPs)后细胞毒性、遗传毒性和免疫毒性的潜在机制,以及 PS-NPs-LZM 相互作用的结合机制。细胞实验结果表明,当蚯蚓免疫细胞暴露于高剂量 PS-NPs 时,会导致活性氧(ROS)的显著释放,从而引发氧化应激。PS-NPs 暴露显著降低了蚯蚓免疫细胞的细胞活力,通过 ROS 介导的氧化应激途径和氧化损伤作用诱导细胞毒性,包括降低抗氧化防御、脂质过氧化、DNA 损伤和蛋白质氧化。此外,PS-NPs 应激通过 ROS 介导的氧化应激途径抑制免疫细胞内 LZM 活性,导致免疫功能受损和免疫毒性。分子研究结果表明,PS-NPs 结合破坏了 LZM 的结构和构象,包括二级结构变化、蛋白质骨架展开/松弛、荧光敏化、微环境变化和颗粒尺寸变化。分子对接表明 PS-NPs 更容易与 LZM 的活性中心结合,并更有效地抑制蛋白质功能,与 TRP62 形成疏水相互作用,TRP62 是与 LZM 功能和构象密切相关的关键氨基酸残基。这也是 LZM 构象变化和功能抑制/失活的原因。本研究结果为采用细胞和分子策略评估 NPs 对土壤生物免疫功能的危害提供了新的视角。