2022
DOI: 10.1016/j.ecoenv.2022.113520
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Polystyrene microplastics induce mitochondrial damage in mouse GC-2 cells

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Cited by 59 publications
(28 citation statements)
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“…MNPs can damage the mitochondrial structure of GC-2 cells, a mouse spermatocyte line, decrease ATP content, diminish membrane potential, and destroy the integrity of the mitochondrial genome, leading to an imbalance in mitochondrial dynamic homeostasis, which induces mitochondrial autophagy. This study explored the effects of MNPs on the mitochondria of germ cell lines, providing support for further research on the effects of MNPs on reproductive health [ 67 ].…”
Section: Toxicities Of Micro- and Nanoplastics On Mitochondriamentioning
confidence: 99%
“…MNPs can damage the mitochondrial structure of GC-2 cells, a mouse spermatocyte line, decrease ATP content, diminish membrane potential, and destroy the integrity of the mitochondrial genome, leading to an imbalance in mitochondrial dynamic homeostasis, which induces mitochondrial autophagy. This study explored the effects of MNPs on the mitochondria of germ cell lines, providing support for further research on the effects of MNPs on reproductive health [ 67 ].…”
Section: Toxicities Of Micro- and Nanoplastics On Mitochondriamentioning
confidence: 99%
“…In all examined samples, near to endoplasmic reticulum vesicles, we found mitochondrial swelling (ballooning cristae or intracristal swelling) next to mitochondrial pyknosis, several myelin figures arising from endoplasmic reticulum, including whorled membranous bodies, which are likely derived from involuting mitochondria ( Figure 6 a–c), and autolysosomes containing mitochondrial remnants and other structures. Interestingly, Liu et al (2022) [ 44 , 62 ] and Ding et al (2021) [ 63 ] also observed changes in mitochondrial ultrastructure and swelling of mitochondrial cristae in mouse spermatocyte line GC-2 and gastric epithelial line GES-1 treated with polystyrene MPs. Mitochondrial swelling and consequent dysfunction are notably involved in the pathogenesis of many human diseases associated with oxidative stress, such as ischemia (infarction)-reperfusion, hypoxia, inflammation, and diabetes, among others.…”
Section: Resultsmentioning
confidence: 99%
“…GI tract exposed MPs and NPs can trigger oxidative stress via reactive oxygen species (ROS) after entering cells (Xie et al, 2020). As the molecular initiation point for the toxicity of MPs and NPs (Hu & Palić, 2020), the generation of ROS has been extensively reported in rodent vitro or in vivo reproductive toxicity studies (Deng et al, 2021; Ijaz et al, 2021; Li et al, 2022; Liu, Hou, Wang, et al, 2022; Liu, Hou, Zhang, et al, 2022; Wei et al, 2021, 2022; Xie et al, 2020). Earlier studies showed that ROS and the oxidative stress ROS generated played an important role in determining cell fate and modifying a range of signal molecules (Zhang et al, 2016).…”
Section: Fertility Toxicity Of Mps and Nps To Rodent And The Mechanismsmentioning
confidence: 99%
“…Earlier studies showed that ROS and the oxidative stress ROS generated played an important role in determining cell fate and modifying a range of signal molecules (Zhang et al, 2016). Oxidative stress occurs when an imbalance between ROS and endogenous antioxidant substances develops, which is revealed directly by the decline of antioxidant enzyme activity, such as CAT, GSH‐PS, SOD, and POD (Ijaz et al, 2021; Li, Wang, et al, 2021; Wei et al, 2022; Xie et al, 2020); the down‐regulation of antioxidant proteins expression levels, such as Nrf2 and HO‐1 (Hou, Wang, et al, 2021; Li et al, 2022; Wei et al, 2021); or the generation of lipid peroxides, such as MDA (Ijaz et al, 2021; Liu, Hou, Wang, et al, 2022; Liu, Hou, Zhang, et al, 2022; Wei et al, 2022; Xie et al, 2020). It is noteworthy that the activity or expression level of these molecules followed a dose‐dependent manner.…”
Section: Fertility Toxicity Of Mps and Nps To Rodent And The Mechanismsmentioning
confidence: 99%