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American Journal of Respiratory Cell and Molecular Biology. Vol. 27, pp. 151-159, 2002
© 2002 American Thoracic Society

Lipid-Mediated Delivery of Oligonucleotide to Pulmonary Endothelium

Zheng Ma, Junlan Zhang, Sean Alber, John Dileo, Yoichi Negishi, Donna Stolz, Simon Watkins, Leaf Huang, Bruce Pitt and Song Li

Center for Pharmacogenetics and Department of Pharmaceutical Sciences, School of Pharmacy; Department of Cell Biology and Physiology, School of Medicine; and Department of Environmental and Occupational Health, Graduate School of Public Health, University of Pittsburgh, Pittsburgh, Pennsylvania

Address correspondence to: Dr. Song Li, Center for Pharmacogenetics, University of Pittsburgh School of Pharmacy, 639 Salk Hall, Pittsburgh, PA 15213. E-mail: sol4{at}pitt.edu

Pulmonary endothelium plays an important role in the maintenance of normal pulmonary physiology and its dysfunction is involved in a number of pulmonary diseases. Correction of endothelial dysfunction via antisense oligodeoxyonucleotides (ODN) is dependent on the development of a delivery vehicle that can efficiently deliver the ODN to pulmonary endothelium with minimal toxicity. To this end, we have developed a lipidic vector (LPD) that is composed of 1,2-dioleoyl-3-trimethylammonium-propane (DOTAP) liposomes, protamine, and ODN. This formulation is highly efficient in delivering ODN to the lung via the vascular route. The efficiency of delivery is a function of lipid composition and of the charge ratio between lipid and ODN. Immunofluorescence staining of BrdU-labeled ODN suggested efficient accumulation of ODN in the alveolar capillary region. Transmission electron microscopy of immunogold localization of BrdU-labeled ODN confirmed that pulmonary endothelial cells were indeed targeted by the vector. Furthermore, this formulation is associated with minimal proinflammatory cytokine response and other hematologic toxicities when the ODN lack a potent unmethylated CpG motif. Pretreatment of mice with LPD containing an ODN against intercellular adhesion molecule-1 (ICAM-1) significantly decreased ICAM-1 expression in the lung following LPS challenge. These results provide a basis for lipid-mediated delivery of ODN for the treatment of pulmonary diseases.

Abbreviations: dioleoylphosphatidyl-ethanolamine, DOPE • 1,2-dioleoyl-3-triethylammonium-propane, DOTAP • intercellular adhesion molecule-1, ICAM-1 • interferon, IFN • interleukin, IL • lipidic vector, LPD • oligodeoxynucleotides, ODN • PBS containing 0.5% bovine serum albumin and 0.15% glycine, PBG • phosphate-buffered saline, PBS




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