» Articles » PMID: 29516282

Comparison of Gene Transfection and Cytotoxicity Mechanisms of Linear Poly(amidoamine) and Branched Poly(ethyleneimine) Polyplexes

Overview
Journal Pharm Res
Specialties Pharmacology
Pharmacy
Date 2018 Mar 9
PMID 29516282
Citations 5
Authors
Affiliations
Soon will be listed here.
Abstract

Purpose: This study aimed to further explore the mechanisms behind the ability of certain linear polyamidoamines (PAAs) to transfect cells with minimal cytotoxicity.

Methods: The transfection efficiency of DNA complexed with a PAA of a molecular weight over 10 kDa or 25 kDa branched polyethyleneimine (BPEI) was compared in A549 cells using a luciferase reporter gene assay. The impact of endo/lysosomal escape on transgene expression was investigated by transfecting cells in presence of bafilomycin A1 or chloroquine. Cytotoxicity caused by the vectors was evaluated by measuring cell metabolic activity, lactate dehydrogenase release, formation of reactive oxygen species and changes in mitochondrial membrane potential.

Results: The luciferase activity was ~3-fold lower after transfection with PAA polyplexes than with BPEI complexes at the optimal polymer to nucleotide ratio (RU:Nt). However, in contrast to BPEI vectors, PAA polyplexes caused negligible cytotoxic effects. The transfection efficiency of PAA polyplexes was significantly reduced in presence of bafilomycin A1 while chloroquine enhanced or decreased transgene expression depending on the RU:Nt.

Conclusions: PAA polyplexes displayed a pH-dependent endo/lysosomal escape which was not associated with cytotoxic events, unlike observed with BPEI polyplexes. This is likely due to their greater interactions with biological membranes at acidic than neutral pH.

Citing Articles

Optimization of chemical transfection in airway epithelial cell lines.

Guo T, Liang W, Singhera G, Memar Vaghri J, Leung J, Dorscheid D BMC Biotechnol. 2025; 25(1):10.

PMID: 39849458 PMC: 11761256. DOI: 10.1186/s12896-025-00945-x.


Cationic Materials for Gene Therapy: A Look Back to the Birth and Development of 2,2-Bis-(hydroxymethyl)Propanoic Acid-Based Dendrimer Scaffolds.

Alfei S Int J Mol Sci. 2023; 24(21).

PMID: 37958989 PMC: 10649874. DOI: 10.3390/ijms242116006.


Correlation between Biophysical Properties of Niosomes Elaborated with Chloroquine and Different Tensioactives and Their Transfection Efficiency.

Sainz-Ramos M, Villate-Beitia I, Gallego I, Al Qtaish N, Menendez M, Lagartera L Pharmaceutics. 2021; 13(11).

PMID: 34834203 PMC: 8623750. DOI: 10.3390/pharmaceutics13111787.


Antimicrobial peptide AR-23 derivatives with high endosomal disrupting ability enhance poly(l-lysine)-mediated gene transfer.

Zhang S, Gong L, Zhang X, Yun Z, Li S, Gao H J Gene Med. 2020; 22(11):e3259.

PMID: 32776410 PMC: 7685122. DOI: 10.1002/jgm.3259.


GHz Ultrasonic Chip-Scale Device Induces Ion Channel Stimulation in Human Neural Cells.

Balasubramanian P, Singh A, Xu C, Lal A Sci Rep. 2020; 10(1):3075.

PMID: 32080204 PMC: 7033194. DOI: 10.1038/s41598-020-58133-0.


References
1.
DE DUVE C, de Barsy T, Poole B, Trouet A, Tulkens P, Van Hoof F . Commentary. Lysosomotropic agents. Biochem Pharmacol. 1974; 23(18):2495-531. DOI: 10.1016/0006-2952(74)90174-9. View

2.
Walker G, Fella C, Pelisek J, Fahrmeir J, Boeckle S, Ogris M . Toward synthetic viruses: endosomal pH-triggered deshielding of targeted polyplexes greatly enhances gene transfer in vitro and in vivo. Mol Ther. 2005; 11(3):418-25. DOI: 10.1016/j.ymthe.2004.11.006. View

3.
Hunter A . Molecular hurdles in polyfectin design and mechanistic background to polycation induced cytotoxicity. Adv Drug Deliv Rev. 2006; 58(14):1523-31. DOI: 10.1016/j.addr.2006.09.008. View

4.
Bowman E, Siebers A, Altendorf K . Bafilomycins: a class of inhibitors of membrane ATPases from microorganisms, animal cells, and plant cells. Proc Natl Acad Sci U S A. 1988; 85(21):7972-6. PMC: 282335. DOI: 10.1073/pnas.85.21.7972. View

5.
Volkl H, Friedrich F, Haussinger D, Lang F . Effect of cell volume on Acridine Orange fluorescence in hepatocytes. Biochem J. 1993; 295 ( Pt 1):11-4. PMC: 1134812. DOI: 10.1042/bj2950011. View