Remote Induction of Cell Autophagy by 2D MoS2 Nanosheets via Perturbing Cell Surface Receptors and mTOR Pathway from Outside of Cells.
Xiaofei ZhouJianbo JiaZhen LuoGaoxing SuTongtao YueBing YanPublished in: ACS applied materials & interfaces (2019)
The ability of nanoparticles to induce adverse consequences in human cells relies on their physical shapes. In this aspect, how two-dimensional nanoparticles differ from three-dimensional nanoparticles is not well-known. To elucidate this difference, combined experimental and theoretical approaches are employed to compare MoS2 nanosheets with 5-layer and 40-layer thicknesses for their cellular effects and the associated molecular events. At a concentration as defined by the nanosheet surface areas (10 cm2/mL), 40-layer nanosheets are internalized by cells, whereas 5-layer nanosheets mostly bind to the cell surface without internalization. Although they alter different autophagy-related genes, a common mechanism is that they both perturb cell surface protein amyloid precursor proteins and activate the mTOR signaling pathway. Our findings prove that the perturbation of cellular function without nanoparticle internalization has significant nanomedicinal and nanotoxicological significances.
Keyphrases
- cell surface
- induced apoptosis
- reduced graphene oxide
- quantum dots
- signaling pathway
- endoplasmic reticulum stress
- highly efficient
- cell cycle arrest
- transition metal
- cell death
- visible light
- oxidative stress
- metal organic framework
- gold nanoparticles
- pi k akt
- cell proliferation
- physical activity
- single cell
- mental health
- emergency department
- cell therapy
- epithelial mesenchymal transition
- mesenchymal stem cells
- walled carbon nanotubes
- bone marrow
- protein protein
- single molecule