Charge-neutralized polyethylenimine-lipid nanoparticles for gene transfer to human embryonic stem cells

被引:0
|
作者
Feng, Guoqing [2 ]
Bai, Yang [1 ,2 ]
Huang, Pengyu [3 ]
Liu, Yuan [4 ]
Yang, Qingbin [2 ]
Li, Bowen [2 ]
Yuan, Qing [5 ]
Qian, Niansong [6 ]
Zheng, Bin [2 ,7 ]
机构
[1] TianJin Med Univ, Dept Stomatol, Gen Hosp, Tianjin 300052, Peoples R China
[2] Tianjin Univ, Acad Med Engn & Translat Med, Tianjin 300072, Peoples R China
[3] Fujian Med Univ, Fujian Matern & Child Hlth Hosp, Fujian Prov Sperm Bank, Coll Clin Med Obstet & Gynecol & Pediat, Fuzhou 350001, Peoples R China
[4] Tianjin Anding Hosp, Tianjin 300222, Peoples R China
[5] Chinese Peoples Liberat Army PLA Gen Hosp, Med Ctr 3, Dept Urol, Beijing 100853, Peoples R China
[6] Eighth Med Ctr Chinese PLA Gen Hosp, Dept Resp, Beijing 100853, Peoples R China
[7] Tianjin Med Univ, Sch Biomed Engn & Technol, Tianjin 300070, Peoples R China
基金
中国国家自然科学基金;
关键词
Cationic lipid; Polyethyleneimine (PEI); Gene delivery; Polycations; Optogenetic manipulation; LINEAR POLYETHYLENIMINE; MANIPULATION; DELIVERY;
D O I
10.1016/j.bmc.2024.118008
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Gene delivery is fundamentally crucial for the genetic manipulation of stem cells. Here, we present a straightforward approach to create a library of charge-neutralized polyethylenimine (PEI)-lipid nanoparticles designed for stem cell transfection. These lipid nanoparticles were formulated using small, branched PEI and lipidic anhydrides. Remarkably, over 15% of the lipid nanoparticles demonstrated high transfection efficiency across various cell types, surpassing the efficiency of both Lipofectamine 2000 and FuGENE HD. A structure-activity analysis indicated that the length and ratio of hydrophobic alkyl substitutions were critical parameters for efficient gene delivery. Notably, the transfection efficiency was higher than that of the original cation PEI. Our optimized PEI-lipid system enabled highly effective plasmid DNA delivery and successfully co-transferred two plasmid DNAs into difficult-to-transfect human embryonic stem cells (hESCs), facilitating optogenetic manipulation within these cells.
引用
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页数:7
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