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Comparison of surfactant and perfluorochemical liquid enhanced adenovirus-mediated gene transfer in normal rat lung

  • Daniel J. Weiss*
  • , Gökhan M. Mutlu
  • , Laura Bonneau
  • , Michael Mendez
  • , Ying Wang
  • , Vidas Dumasius
  • , Phillip Factor
  • *Corresponding author for this work
  • University of Washington
  • Evanston Northwestern Healthcare
  • Northwestern University

Research output: Contribution to journalArticlepeer-review

12 Scopus citations

Abstract

Both surfactant- and perfluorochemical (PFC)-based vehicles enhance adenovirus-mediated gene transfer in the lung. To compare the relative effects of surfactant and PFC liquid, we infected orotracheally intubated Sprague-Dawley rats with 4 × 109 pfu of an E1a-/E3- adenovirus expressing either an Escherichia coli lacZ (AdlacZ) mini-gene or no cDNA Adnull). Surfactant-mediated delivery was achieved via instillation of four, 200-μl aliquots of virus suspended in a 50% surfactant (Survanta) vehicle over a 15-minute period. PFC rats received virus in 100 μl of saline followed by instillation of the PFC liquid FC-75 (10 cc/kg body weight) over a 2- to 3- minute period. Lungs were collected 3 days later for measurement of β-galactosidase (β-gal) expression and indices of inflammation. Both PFC liquid and surfactant-based vehicles produced widespread β-gal expression and increased total β-gal activity over that observed with instillation of vector alone. Both vehicles comparably increased bronchoalveolar lavage fluid (BALF), total cell counts, neutrophils, total protein, and IFNγ. FC-75 was also associated with increased BALF IL1β. In conclusion, surfactant and FC-75 are similarly effective vehicles for adenovirus-mediated gene transfer to the lung.

Original languageEnglish
Pages (from-to)43-49
Number of pages7
JournalMolecular Therapy
Volume6
Issue number1
DOIs
StatePublished - 1 Jul 2002
Externally publishedYes

Keywords

  • Adenovirus
  • FC-75
  • Gene transfer
  • Lung
  • Perfluorochemical liquid
  • Surfactant
  • Survanta
  • β-galactosidase

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