Literature DB >> 9076661

Effects of cationic liposome-DNA complexes on pulmonary surfactant function in vitro and in vivo.

P Boncuk1, M Kaser, Y Yu, H W Taeusch.   

Abstract

Cationic liposome-DNA complexes are being evaluated as potential gene therapy agents for the lung. Cations have strong effects on the biophysical functions of lung surfactant. Therefore, we assessed whether cationic liposomes [composed of N-(1-(2,3-dioleyloxy) propyl)-N,N,N-trimethyl-ammonium chloride and dioleylphosphatidylethanolamine] with or without DNA affect behavior of four types of surfactant in vitro. Experiments were carried out using a modified Wilhelmy surface balance. The ability of surfactants that contain protein and anionic lipids to lower surface tension was inhibited in the presence of cationic liposomes. Inactivation was less when DNA was preincubated with cationic liposomes. Surfactant that contained neither protein nor anionic lipids was not inactivated. Mechanical properties of the lung were studied to assess in vivo surfactant function after intratracheal instillation of a cationic liposome-DNA complex into adult rats. Pressure-volume deflation curves were shifted by 18% compared with those from normal (untreated) animals, but this effect was transient and not different from that observed in animals who received a similar volume of saline. These findings indicate that cationic liposomes alone may have deleterious effects on behavior of some surfactants possibly by disrupting charge interactions between negatively charged phospholipids and surfactant proteins. When DNA is added to liposomes before exposure to surfactants, the adverse charge interactions may be obviated by charge neutralization of liposomes by DNA.

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Year:  1997        PMID: 9076661     DOI: 10.1007/s11745-997-0031-2

Source DB:  PubMed          Journal:  Lipids        ISSN: 0024-4201            Impact factor:   1.880


  23 in total

1.  Interactions of mammalian cells with lipid dispersions containing novel metabolizable cationic amphiphiles.

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Journal:  Biochim Biophys Acta       Date:  1990-03-30

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Authors:  K L Brigham; B Meyrick; B Christman; M Magnuson; G King; L C Berry
Journal:  Am J Med Sci       Date:  1989-10       Impact factor: 2.378

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Authors:  A E Canonico; J T Conary; B O Meyrick; K L Brigham
Journal:  Am J Respir Cell Mol Biol       Date:  1994-01       Impact factor: 6.914

6.  Non-invasive liposome-mediated gene delivery can correct the ion transport defect in cystic fibrosis mutant mice.

Authors:  E W Alton; P G Middleton; N J Caplen; S N Smith; D M Steel; F M Munkonge; P K Jeffery; D M Geddes; S L Hart; R Williamson
Journal:  Nat Genet       Date:  1993-10       Impact factor: 38.330

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Journal:  Chem Phys Lipids       Date:  1983-07       Impact factor: 3.329

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Authors:  H Efrati; S Hawgood; M C Williams; K Hong; B J Benson
Journal:  Biochemistry       Date:  1987-12-01       Impact factor: 3.162

9.  Reversible and irreversible inactivation of preformed pulmonary surfactant surface films by changes in subphase constituents.

Authors:  J D Amirkhanian; H W Taeusch
Journal:  Biochim Biophys Acta       Date:  1993-01-10

10.  Cationic lipids for reporter gene and CFTR transfer to rat pulmonary epithelium.

Authors:  J J Logan; Z Bebok; L C Walker; S Peng; P L Felgner; G P Siegal; R A Frizzell; J Dong; M Howard
Journal:  Gene Ther       Date:  1995-01       Impact factor: 5.250

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  1 in total

1.  The mRNA-LNP platform's lipid nanoparticle component used in preclinical vaccine studies is highly inflammatory.

Authors:  Sonia Ndeupen; Zhen Qin; Sonya Jacobsen; Aurélie Bouteau; Henri Estanbouli; Botond Z Igyártó
Journal:  iScience       Date:  2021-11-20
  1 in total

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