Xu Tao, Wang Suhang, Shao Zhengzhong
State Key Laboratory of Molecular Engineering of Polymer Advanced Materials Laboratory, Department of Macromolecular Science, Fudan University, Shanghai, 200433, People's Republic of China.
Pharm Res. 2014 Apr;31(4):895-907. doi: 10.1007/s11095-013-1211-4. Epub 2013 Oct 8.
The structure-function relationship and mechanism of polycations as gene carriers have attracted considerable research interest in recent years. The present study was to investigate the relationship between polycation chain length and transfection efficiency (RCL-TE), and the corresponding mechanism by O-methyl-free N,N,N-trimethyl chitosans (TMCs) as gene carriers.
Four TMCs with various chain lengths were synthesized and used to evaluate the RCL-TE. To investigate the details of RCL-TE, a number of factors such as cytotoxicity, cellular uptake efficiency, cellular uptake pathway and intracellular trafficking, were evaluated.
In comparison to short chain length TMCs (S-TMCs), long chain length ones (L-TMCs) mediated higher gene expression. The polyplexes formed by L-TMCs and pDNA showed higher stability. The cellular uptake pathway and intracellular trafficking of these TMC/pDNA polyplexes were different. These above factors are probably the key ones in RCL-TE rather than polycation-DNA binding affinity, polyplex particle size in water, zeta potential, serum, cytotoxicity, and cellular uptake efficiency.
For rational design of chitosan-based polycations as gene carriers, polycations with relative long chain lengths are more favorable and more attention should be paid to polyplex stability, function of uncomplexed polycation chains, cellular uptake pathway, and intracellular trafficking.
近年来,聚阳离子作为基因载体的结构-功能关系及机制引起了广泛的研究兴趣。本研究旨在以无O-甲基的N,N,N-三甲基壳聚糖(TMCs)作为基因载体,研究聚阳离子链长与转染效率(RCL-TE)之间的关系及其相应机制。
合成了四种不同链长的TMCs,并用于评估RCL-TE。为了探究RCL-TE的详细情况,对细胞毒性、细胞摄取效率、细胞摄取途径和细胞内运输等多个因素进行了评估。
与短链长度的TMCs(S-TMCs)相比,长链长度的TMCs(L-TMCs)介导更高的基因表达。L-TMCs与pDNA形成的多聚体表现出更高的稳定性。这些TMC/pDNA多聚体的细胞摄取途径和细胞内运输有所不同。上述因素可能是RCL-TE的关键因素,而非聚阳离子与DNA的结合亲和力、水中多聚体粒径、zeta电位、血清、细胞毒性和细胞摄取效率。
为合理设计基于壳聚糖的聚阳离子作为基因载体,相对长链长度的聚阳离子更有利,应更多关注多聚体稳定性、未复合聚阳离子链的功能、细胞摄取途径和细胞内运输。