转染
脂质体
内体
基因传递
化学
DNA缩合
细胞毒性
细胞生物学
DNA
基因
细胞培养
细胞
分子生物学
生物化学
体外
生物
遗传学
载体(分子生物学)
重组DNA
作者
Delu Che,Chenfei Wang,Zhili Li,Kaixuan Wang,Shuaiwei Sun,Xinyue Zhang,Yi Li,Zhengju Chen,Lei Guo,Yajing Hou,Dezhong Zhou,Songmei Geng
标识
DOI:10.1016/j.cclet.2022.108066
摘要
Suspension cells play a crucial role in many biological processes. However, compared to adherent cells, it is particularly challenging to introduce exogenous genes into suspension cells to regulate their biological functions with non-viral gene vectors, mainly due to the low cellular uptake and endosomal escape of polyplexes. Herein, to improve the interactions of polyplexes with cellular membranes, we design and synthesize highly branched poly(β-amino ester) (HPAE) via an "A2 + B4 + C2" Michael addition strategy. Results show that branching significantly increases DNA condensation of HPAE, cellular uptake and endosomal escape of HPAE/DNA polyplexes. In mast cells (MCs), HPAE exhibits up to 80-fold higher gene transfection efficiency compared to the corresponding linear poly(β-amino ester) (LPAE) and the leading commercial gene transfection reagents PEI25k, jetPEI, and Lipofectamine 3000, without causing obvious cytotoxicity. Our study establishes a reliable non-viral platform for efficient gene transfection of suspension cells.
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