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
相关论文
共 30 条
[11]   The role of surface charge in cellular uptake and cytotoxicity of medical nanoparticles [J].
Froehlich, Eleonore .
INTERNATIONAL JOURNAL OF NANOMEDICINE, 2012, 7 :5577-5591
[12]   Gene delivery platforms [J].
Kim, Jong-Myung ;
Shin, Eunkyoung ;
Ryou, Sang-Mi ;
Yeom, Ji-Hyun ;
Lee, Kangseok .
BIOTECHNOLOGY AND BIOPROCESS ENGINEERING, 2013, 18 (04) :637-647
[13]   The targeted intracellular delivery of cytochrome C protein to tumors using lipid-apolipoprotein nanoparticles [J].
Kim, Sang Kyoon ;
Foote, Michael B. ;
Huang, Leaf .
BIOMATERIALS, 2012, 33 (15) :3959-3966
[14]   The release of cytochrome c from mitochondria: A primary site for Bcl-2 regulation of apoptosis [J].
Kluck, RM ;
BossyWetzel, E ;
Green, DR ;
Newmeyer, DD .
SCIENCE, 1997, 275 (5303) :1132-1136
[15]   Synthesis and characterization of a series of carbamate-linked cationic lipids for gene delivery [J].
Liu, DL ;
Hu, JJ ;
Qiao, WH ;
Li, ZS ;
Zhan, SB ;
Cheng, LB .
LIPIDS, 2005, 40 (08) :839-848
[16]   Hydration properties of lamellar and non-lamellar phases of phosphatidylcholine and phosphatidylethanolamine [J].
McIntosh, TJ .
CHEMISTRY AND PHYSICS OF LIPIDS, 1996, 81 (02) :117-131
[17]   Delivery of Chemically Glycosylated Cytochrome c Immobilized in Mesoporous Silica Nanoparticles Induces Apoptosis in HeLa Cancer Cells [J].
Mendez, Jessica ;
Cruz, Moraima Morales ;
Delgado, Yamixa ;
Figueroa, Cindy M. ;
Orellano, Elsie A. ;
Morales, Myraida ;
Monteagudo, Alina ;
Griebenow, Kai .
MOLECULAR PHARMACEUTICS, 2014, 11 (01) :102-111
[18]   ENGINEERING CATIONIC LIPOSOME: SIRNA COMPLEXES FOR IN VITRO AND IN VIVO DELIVERY [J].
Podesta, Jennifer E. ;
Kostarelos, Kostas .
METHODS IN ENZYMOLOGY; LIPOSOMES, PT F, 2009, 464 :343-354
[19]   Emerging roles of caspase-3 in apoptosis [J].
Porter, AG ;
Jänicke, RU .
CELL DEATH AND DIFFERENTIATION, 1999, 6 (02) :99-104
[20]   Activation of apoptosis signalling pathways by reactive oxygen species [J].
Redza-Dutordoir, Maureen ;
Averill-Bates, Diana A. .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH, 2016, 1863 (12) :2977-2992