Encapsulation of Apoptotic Proteins in Lipid Nanoparticles to Induce Death of Cancer Cells

被引:16
作者
Bae, Chun-Sik [1 ]
Lee, Chang-Min [1 ]
Ahn, Taeho [1 ]
机构
[1] Chonnam Natl Univ, Coll Vet Med, Gwangju 61186, South Korea
基金
新加坡国家研究基金会;
关键词
apoptosis; cell death; cytochrome c; DOTAP; nanoparticle; reactive oxygen species; CYTOCHROME-C; CATIONIC LIPIDS; DELIVERY; LIPOSOMES; VESICLES; BAX; ROS;
D O I
10.1007/s12257-019-0409-7
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
According to previous reports, cationic nanoparticles (cNPs) consisting of 1,2-dioleoyl-3-trimethylammonium-propane (DOTAP), a cationic lipid, without any cargos, induce generation of reactive oxygen species (ROS) and toxicity in cells. We investigated the effect of DOTAP-based cNPs containing encapsulated human pro-apoptotic proteins (P-cNPs), tBid, Bax, or cytochrome c (Cyt c) on the death of HepG2, cancer cells. Upon the treatment to cells, cNPs containing Cyt c-cargo were the most effective in inducing cell death, followed by tBid- and Bax-cNPs. Among three P-cNPs, Cyt c-cNPs also induced the highest levels of ROS production and caspase-3 activity in the cells under the treatment with the same DOTAP concentration. The incorporation of dioleoylglycerol (DOG), a neutral phospholipid, in cNPs at the expense of DOTAP resulted in an increased amount of the encapsulated protein and consequently enhanced cell death in a DOG concentration-dependent manner. Thus, the present cNP formulation with protein cargo may elicit apoptotic effects in cancer cells and serve as a rational background for the preparation of cationic lipid-based NP formulation for cancer treatment.
引用
收藏
页码:264 / 271
页数:8
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