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纳米级微塑料暴露通过触发 GSDMD 的线粒体定位诱导皮肤细胞衰老。

Nano-sized microplastics exposure induces skin cell senescence via triggering the mitochondrial localization of GSDMD.

机构信息

The First Department of Oral and Maxillofacial Surgery & Oral Plastic and Aesthetic Surgery, Hospital of Stomatology, Jilin University, Changchun, China.

Histology and Embryology, College of Basic Medical Sciences, Jilin University, Changchun, China.

出版信息

Environ Pollut. 2024 May 15;349:123874. doi: 10.1016/j.envpol.2024.123874. Epub 2024 Mar 27.

Abstract

Nano-sized microplastic pollution is distributed worldwide. Nano-sized microplastics can enter the blood through the digestive tract, and then transported to various tissues and organs of the body, resulting in a series of toxicological effects. In addition, nano-sized microplastics can penetrate the skin barrier. However, the toxicological effects of nano-sized microplastics on the skin are still not completely understood. Two skin cell lines were used as in vitro models to investigate the toxicological effects of nano-sized microplastics on skin cells and their potential molecular mechanisms. First, cellular behavioral research results showed that nano-sized microplastics can be internalized into skin cells in a time- and dose-dependent manner. Further experiments using western blotting, indirect immunofluorescence, and ELISA assays demonstrated that nano-sized microplastics cause an increase in skin cell inflammation levels. Additionally, our research showed that nano-sized microplastics caused skin cell senescence damage by evaluating aging-marker molecules such as p16 and p21. Subsequently, we studied the potential molecular mechanism by which nano-sized microplastics cause pathological skin injury and found that they induce mitochondrial oxidative stress, depolarize the mitochondrial membrane potential, and recruit GSDMD to the mitochondria. Subsequently, mtDNA enters the cytoplasm via GSDMD pores, which then activates the AIM2 Inflammasome. Ultimately, it causes a series of biochemical reactions such as inflammation and aging in cells. In an in vivo model, we tested the effect of nano-sized microplastics on skin regeneration and found that they acted as an inhibitor to skin regeneration and aggravated the inflammatory reaction of the skin. Overall, our results provide new evidence of the skin toxicity of nano-sized microplastics. This study provides a theoretical foundation for further research on the potential toxicological effects of nano-sized microplastics on the skin.

摘要

纳米级微塑料污染分布于全球各地。纳米级微塑料可通过消化道进入血液,并进一步被运输到身体的各个组织和器官,引发一系列的毒理学效应。此外,纳米级微塑料还可以穿透皮肤屏障。然而,纳米级微塑料对皮肤的毒理学效应尚不完全清楚。本研究使用两种皮肤细胞系作为体外模型,以研究纳米级微塑料对皮肤细胞的毒理学效应及其潜在的分子机制。首先,细胞行为学研究结果表明,纳米级微塑料可以时间和剂量依赖的方式被内化进入皮肤细胞。进一步使用western blot、间接免疫荧光和 ELISA 实验证实,纳米级微塑料可引起皮肤细胞炎症水平的升高。此外,我们的研究还通过评估衰老标志物分子(如 p16 和 p21),表明纳米级微塑料可导致皮肤细胞衰老损伤。随后,我们研究了纳米级微塑料导致皮肤病理性损伤的潜在分子机制,发现其可诱导线粒体氧化应激,使线粒体膜电位去极化,并招募 GSDMD 到线粒体。随后,GSDMD 孔允许 mtDNA 进入细胞质,进而激活 AIM2 炎症小体。最终,导致细胞内发生一系列的生化反应,如炎症和衰老。在体内模型中,我们测试了纳米级微塑料对皮肤再生的影响,发现其作为皮肤再生的抑制剂,加剧了皮肤的炎症反应。总的来说,本研究结果为纳米级微塑料的皮肤毒性提供了新的证据。本研究为进一步研究纳米级微塑料对皮肤潜在的毒理学效应提供了理论基础。

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