2012
DOI: 10.1016/j.biomaterials.2012.05.064
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Simultaneous induction of autophagy and toll-like receptor signaling pathways by graphene oxide

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Cited by 219 publications
(170 citation statements)
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“…However, degradation of the autophagic substrate p62 protein was also inhibited by both nanomaterials [31]. Chen's researches demonstrated that GO treatment of cells simultaneously triggers autophagy and TLR4/TLR9-regulated inflammatory responses and the autophagy was at least partly regulated by the TLRs pathway [32].…”
Section: Autophagy and Nanomaterialsmentioning
confidence: 99%
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“…However, degradation of the autophagic substrate p62 protein was also inhibited by both nanomaterials [31]. Chen's researches demonstrated that GO treatment of cells simultaneously triggers autophagy and TLR4/TLR9-regulated inflammatory responses and the autophagy was at least partly regulated by the TLRs pathway [32].…”
Section: Autophagy and Nanomaterialsmentioning
confidence: 99%
“…Clathrin mediated endocytosis inhibitors significantly suppressed MWCNT uptake, whereas caveolae mediated endocytosis and macropinocytosis were also found to be involved in MWCNT uptake. Thus, MWCNTs were positively taken up by nonphagocytic cells, and their cytotoxicity was closely related to these three endocytosis pathways [57].Chen GY demonstrated that GO treatment of cells simultaneously triggers autophagy and TLR4/TLR9-regulated inflammatory responses, and the autophagy was at least partly regulated by the TLRs pathway, suggesting a mechanism by which cells respond to nanomaterials and underscores the importance of future safety evaluation of nanomaterials [32].Citation: Liu Y, Wang J, Jiang M, Tong X, Han C, et al (2017) The Role of Cell Autophagy in Toxicity Caused by Dental Nanomaterials. J Nanotechnol Nanomed Nanobiotechnol 4: 011.…”
mentioning
confidence: 98%
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“…Similarly, Stephan et al [40] showed that cell death upon exposure to C 60 (OH) 24 was related with cytoskeleton disruption, loss of mitochondrial capacity and autophagic vacuole accumulation. Indeed, ATP depletion and loss of mitochondrial potential were partially ameliorated when Graphene oxide 2.4 μm and 350 nm RAW264.7 cells TEM, LC3 [44] cells were co-treated with C 60 (OH) 24 and an autophagy inhibitor (3-methyladenine).…”
Section: And C 60 Derivativesmentioning
confidence: 99%
“…Therefore, more and more studies started focusing on the biosafety and cytotoxicity of graphene. Recently, Chen et al [44] demonstrated that graphene oxide (GO) could induce autophagy in macrophage RAW264.7 cells and the effect was concentration-dependent. They observed the appearance of autophagic vacuoles and activation of LC3-II.…”
Section: Graphenementioning
confidence: 99%