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多壁碳纳米管(MWCNTs)在转化生长因子-β(TGF-β)刺激的肺上皮细胞中引发细胞衰老。

Multi-Walled Carbon Nanotubes (MWCNTs) Cause Cellular Senescence in TGF-β Stimulated Lung Epithelial Cells.

作者信息

Lucas Joseph H, Wang Qixin, Muthumalage Thivanka, Rahman Irfan

机构信息

Department of Environmental Medicine, School of Medicine and Dentistry, University of Rochester Medical Center, Rochester, NY 14642, USA.

出版信息

Toxics. 2021 Jun 19;9(6):144. doi: 10.3390/toxics9060144.

Abstract

Multi-walled carbon nanotubes are engineered nanomaterials (ENMs) that have a fiber-like structure which may be a concern for the development of cellular senescence. Premature senescence, a state of irreversible cell cycle arrest, is implicated in the pathogenesis of chronic lung diseases such as pulmonary fibrosis (PF). However, the crosstalk between downstream pathways mediating fibrotic and senescent responses of MWCNTs is not well-defined. Here, we exposed human bronchial epithelial cells (BEAS-2B) to MWCNTs for up to 72 h and demonstrate that MWCNTs increase reactive oxygen species (ROS) production accompanied by inhibition of cell proliferation. In addition, MWCNT exposure resulted in the increase of p21 protein abundance and senescence associated β-galactosidase (SA β-gal) activity. We also determined that co-exposure with the cytokine, transforming growth factor-β (TGF-β) exacerbated cellular senescence indicated by increased protein levels of p21, p16, and γH2A.X. Furthermore, the production of fibronectin and plasminogen activator inhibitor (PAI-1) was significantly elevated with the co-exposure compared to MWCNT or TGF-β alone. Together, our study suggests that the cellular senescence potential of MWCNTs may be enhanced by pro-fibrotic mediators, such as TGF-β in the surrounding microenvironment.

摘要

多壁碳纳米管是一种工程纳米材料(ENM),具有纤维状结构,可能与细胞衰老的发生有关。早衰是一种不可逆的细胞周期停滞状态,与诸如肺纤维化(PF)等慢性肺部疾病的发病机制有关。然而,介导多壁碳纳米管纤维化和衰老反应的下游信号通路之间的相互作用尚未明确。在此,我们将人支气管上皮细胞(BEAS-2B)暴露于多壁碳纳米管中长达72小时,结果表明多壁碳纳米管会增加活性氧(ROS)的产生,并伴随细胞增殖受到抑制。此外,暴露于多壁碳纳米管会导致p21蛋白丰度增加以及衰老相关β-半乳糖苷酶(SA β-gal)活性增强。我们还确定,与细胞因子转化生长因子-β(TGF-β)共同暴露会加剧细胞衰老,这表现为p21、p16和γH2A.X蛋白水平升高。此外,与单独暴露于多壁碳纳米管或TGF-β相比,共同暴露时纤连蛋白和纤溶酶原激活物抑制剂(PAI-1)的产生显著增加。总之,我们的研究表明,诸如周围微环境中的TGF-β等促纤维化介质可能会增强多壁碳纳米管的细胞衰老潜能。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bf9d/8234672/e013f31feb85/toxics-09-00144-g0A1.jpg

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