2D MoS 2 and BN Nanosheets Damage Mitochondria through Membrane Penetration.
Kangqiang QiuWeiwei ZouZhou FangYuxin WangSam BellXiang ZhangZhiqi TianXiuqiong XuBaohua JiDechang LiTaosheng HuangJiajie DiaoPublished in: ACS nano (2023)
With the progression of nanotechnology, a growing number of nanomaterials have been created and incorporated into organisms and ecosystems, which raises significant concern about potential hazards of these materials on human health, wildlife, and the environment. Two-dimensional (2D) nanomaterials are one type of nanomaterials with thicknesses ranging from that of a single atom or of several atoms and have been proposed for a variety of biomedical applications such as drug delivery and gene therapy, but the toxicity thereof on subcellular organelles remains to be studied. In this work, we studied the impact of two typical 2D nanomaterials, MoS 2 and BN nanosheets, on mitochondria, which are a type of membranous subcellular organelle that provides energy to cells. While 2D nanomaterials at a low dose exhibited a negligible cell mortality rate, significant mitochondrial fragmentation and partially reduced mitochondrial functions occurred; cells initiate mitophagy in response to mitochondrial damages, which cleans damaged mitochondria to avoid damage accumulation. Moreover, the molecular dynamics simulation results revealed that both MoS 2 and BN nanosheets can spontaneously penetrate the mitochondrial lipid membrane through the hydrophobic interaction. The membrane penetration induced heterogeneous lipid packing resulting in damages. Our results demonstrate that even at a low dose 2D nanomaterials can physically damage mitochondria by penetrating the membrane, which draws attention to carefully evaluating the cytotoxicity of 2D nanomaterials for the potential biomedical application.
Keyphrases
- oxidative stress
- low dose
- induced apoptosis
- human health
- quantum dots
- reduced graphene oxide
- cell death
- molecular dynamics simulations
- drug delivery
- diabetic rats
- risk assessment
- gene therapy
- highly efficient
- cell cycle arrest
- endoplasmic reticulum
- climate change
- visible light
- single cell
- room temperature
- stem cells
- type diabetes
- gold nanoparticles
- endoplasmic reticulum stress
- cardiovascular disease
- metal organic framework
- coronary artery disease
- gram negative
- cardiovascular events
- cell proliferation
- signaling pathway
- high glucose
- ionic liquid
- bone marrow
- multidrug resistant