膜
溶血
体外
化学
脂质体
生物物理学
生物化学
细胞生物学
生物
免疫学
作者
Yuwei He,Ruixiang Li,Haichun Li,Shuya Zhang,Wentao Dai,Qian Wu,Lixian Jiang,Zicong Zheng,Shun Shen,Xing Chen,Yuefei Zhu,Jianxin Wang,Zhiqing Pang
出处
期刊:ACS Nano
[American Chemical Society]
日期:2019-03-11
卷期号:13 (4): 4148-4159
被引量:70
标识
DOI:10.1021/acsnano.8b08964
摘要
Pore-forming toxins (PFTs) are the most common bacterial virulence proteins and play a significant role in the pathogenesis of bacterial infections; thus, PFTs are an attractive therapeutic target in bacterial infections. Inspired by the pore-forming process and mechanism of PFTs, we designed an integrated hybrid nanovesicle—the erythroliposome (called the RM-PL)—for PFT detoxification by fusing natural red blood cell (RBC) membranes with artificial lipid membranes. The lipid and RBC membranes were mutually beneficial when integrated into a hybrid nanovesicle structure. The RBC membrane endowed RM-PLs with the capacity for detoxification, while the PEGylated lipid membrane stabilized the RM-PLs and greatly improved the detoxification capacity of the RBC membrane. With α-hemolysin (Hlα) as a model PFT, we demonstrated that RM-PLs could not only significantly reduce the toxicity of Hlα to erythrocytes in vitro but also effectively sponge Hlα in vivo and rescue mice from Hlα-induced damage. Moreover, the high detoxification capacity of RM-PLs was shown to be partly related to the expression of the Hlα receptor protein, a disintegrin and metalloproteinase domain-containing protein 10 on the RBC membrane. Consequently, as a component integrating natural and artificial materials, the erythroliposome nanoplatform inspires potential strategies for antivirulence therapy.
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