Abstract
Lipoplexes containing a mixture of cationic phospholipids dioleoylethylphosphatidylcholine (EDOPC) and dilauroylethylphosphatidylcholine (EDLPC) are known to be far more efficient agents in transfection of cultured primary endothelial cells than are lipoplexes containing either lipid alone. The large magnitude of the synergy permits comparison of the physical and physico-chemical properties of lipoplexes that have very different transfection efficiencies, but minor chemical differences. Here we report that the superior transfection efficiency of the EDLPC/EDOPC lipoplexes correlates with higher surface activity, higher affinity to interact and mix with negatively charged membrane-mimicking liposomes, and with considerably more efficient DNA release relative to the EDOPC lipoplexes. Observations on cultured cells agree with the results obtained with model systems; confocal microscopy of transfected human umbilical artery endothelial cells (HUAEC) demonstrated more extensive DNA release into the cytoplasm and nucleoplasm for the EDLPC/EDOPC lipoplexes than for EDOPC lipoplexes; electron microscopy of cells fixed and embedded directly on the culture dish revealed contact of EDLPC/EDOPC lipoplexes with various cellular membranes, including those of the endoplasmic reticulum, mitochondria and nucleus. The sequence of events outlining efficient lipofection is discussed based on the presented data.
Original language | English (US) |
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Pages (from-to) | 375-386 |
Number of pages | 12 |
Journal | Biochimica et Biophysica Acta - Biomembranes |
Volume | 1768 |
Issue number | 2 |
DOIs | |
State | Published - Feb 2007 |
Funding
NIH grant GM52329 provided primary funding for this research, and NIH grant GM57305 provided some important additional support. We thank Robert A. Lamb (Northwestern University) for access to the flow cytometer instrument, William Russin (Northwestern University) for technical support in confocal microscopy, and Harsh Parikh and Yaeko Hiyama (Northwestern University) for synthesis of cationic lipids. BioCAT is a NIH-supported Research Center, through Grant RR08630. Use of the Advanced Photon Source was supported by the U.S. Department of Energy, Basic Energy Sciences, Office of Energy Research under Contract No. W-31-102-Eng-38. DND-CAT is supported by E.I. DuPont de Nemours and Co., The Dow Chemical Company, NSF Grant DMR-9304725, and the State of Illinois through the Department of Commerce and the Board of Higher Education Grant IBHE HECA NWU 96. Use of APS was supported by the U.S. DOE, Basic Energy Sciences, Office of Energy Research, Contract No. W-31-102-Eng-38.
Keywords
- Cationic lipid
- DNA unbinding
- Gene therapy
- Lipofection
- Membrane fusion
- Surface tension
ASJC Scopus subject areas
- Biophysics
- Biochemistry
- Cell Biology