Enhanced liver uptake of opsonized red blood cells after in vivo transfer of FcgammaRIIA cDNA to the liver. Academic Article uri icon

Overview

MeSH

  • Animals
  • Cells, Cultured
  • DNA, Complementary
  • Female
  • Gene Transfer Techniques
  • Rats
  • Rats, Sprague-Dawley

MeSH Major

  • Antigens, CD
  • Erythrocytes
  • Liver
  • Phagocytosis
  • Receptors, IgG

abstract

  • Fcgamma receptors convey to phagocytic cells the ability to recognize, bind, and internalize IgG-coated cells and microorganisms. The present study demonstrates the use of adenovirus (Ad)-mediated gene transfer of human Fcgamma receptor IIA cDNA to convert normally nonphagocytic cells (hepatocytes) into functional equivalents of phagocytic cells. Ad vector in vitro transfer and expression of FcgammaRIIA cDNA in primary rat hepatocytes was confirmed by flow cytometry anti-FcgammaRIIA immunodetection, and the function of the receptor was demonstrated by enhanced binding and phagocytosis of (51)Cr-labeled IgG-opsonized erythrocytes. After in vivo gene transfer to rats, expression of FcgammaRIIA cDNA in hepatocytes was confirmed by Northern analysis and immunohistochemistry. Rats infected with the Ad vector carrying the FcgammaRIIA cDNA demonstrated enhanced clearance of opsonized erythrocytes, but not nonopsonized erythrocytes, from the circulation with increased sequestration within the liver. Together, these data demonstrate that Ad-mediated FcgammaRIIA gene transfer can convert normally IgG-nonphagocytic cells into phagocytic cells capable of recognizing, binding, and ingesting an opsonized particulate antigen, suggesting that gene transfer strategies might be used to transiently augment host defense by enhancing the clearance of immune complexes.

publication date

  • November 15, 1999

has subject area

  • Animals
  • Antigens, CD
  • Cells, Cultured
  • DNA, Complementary
  • Erythrocytes
  • Female
  • Gene Transfer Techniques
  • Liver
  • Phagocytosis
  • Rats
  • Rats, Sprague-Dawley
  • Receptors, IgG

Research

keywords

  • Journal Article

Identity

Language

  • eng

PubMed ID

  • 10552955

Additional Document Info

start page

  • 3448

end page

  • 3455

volume

  • 94

number

  • 10