NIR-II Light-Driven Genetically Engineered Exosome Nanocatalysts for Efficient Phototherapy against Glioblastoma.
Xueyang FangRui GongDecai YangChenxi LiYuanyuan ZhangYan WangGuohui NieMingle LiXiaojun PengBin ZhangPublished in: Journal of the American Chemical Society (2024)
Glioblastoma (GBM) poses a significant therapeutic challenge due to its invasive nature and limited drug penetration through the blood-brain barrier (BBB). In response, here we present an innovative biomimetic approach involving the development of genetically engineered exosome nanocatalysts (Mn@Bi 2 Se 3 @RGE-Exos) for efficient GBM therapy via improving the BBB penetration and enzyme-like catalytic activities. Interestingly, a photothermally activatable multiple enzyme-like reactivity is observed in such a nanosystem. Upon NIR-II light irradiation, Mn@Bi 2 Se 3 @RGE-Exos are capable of converting hydrogen peroxide into hydroxyl radicals, oxygen, and superoxide radicals, providing a peroxidase (POD), oxidase (OXD), and catalase (CAT)-like nanocatalytic cascade. This consequently leads to strong oxidative stresses to damage GBM cells. In vitro, in vivo, and proteomic analysis further reveal the potential of Mn@Bi 2 Se 3 @RGE-Exos for the disruption of cellular homeostasis, enhancement of immunological response, and the induction of cancer cell ferroptosis, showcasing a great promise in anticancer efficacy against GBM with a favorable biosafety profile. Overall, the success of this study provides a feasible strategy for future design and clinical study of stimuli-responsive nanocatalytic medicine, especially in the context of challenging brain cancers like GBM.
Keyphrases
- hydrogen peroxide
- nitric oxide
- blood brain barrier
- fluorescent probe
- fluorescence imaging
- photodynamic therapy
- room temperature
- induced apoptosis
- cell death
- cell cycle arrest
- white matter
- stem cells
- drug release
- genome wide
- young adults
- metal organic framework
- multiple sclerosis
- single cell
- big data
- cell proliferation
- resting state
- gene expression
- artificial intelligence
- smoking cessation
- bone marrow
- cerebral ischemia
- endoplasmic reticulum stress
- drug induced
- crystal structure
- subarachnoid hemorrhage
- bone regeneration