Infection of endothelium with E1(-)E4(+), but not E1(-)E4(-), adenovirus gene transfer vectors enhances leukocyte adhesion and migration by modulation of ICAM-1, VCAM-1, CD34, and chemokine expression. Academic Article uri icon

Overview

MeSH

  • Adenoviridae
  • Antigens, CD34
  • Cell Adhesion
  • Cell Movement
  • Cells, Cultured
  • Chemokines
  • Down-Regulation
  • Gene Expression Regulation
  • Genetic Vectors
  • Humans
  • Intercellular Adhesion Molecule-1
  • Receptors, Cell Surface
  • Time Factors
  • Transfection
  • Up-Regulation
  • Vascular Cell Adhesion Molecule-1

MeSH Major

  • Adenovirus E1 Proteins
  • Adenovirus E4 Proteins
  • Endothelium, Vascular
  • Leukocytes
  • Proteins

abstract

  • Intravascular introduction of replication-deficient adenoviral vectors (Advectors) provides an ideal model of delivery of transgenes for the treatment of various vascular abnormalities. On the basis of the knowledge that Advectors can induce inflammatory responses after intravascular administration, we speculated that cellular activation by Advector infection could directly modulate the endothelial cell (EC) adhesion molecule/chemokine expression repertoire. Infection of human umbilical vein ECs or bone marrow microvascular ECs with an E1(-)E4(+) Advector resulted in the upregulation of intercellular adhesion molecule-1 (ICAM-1), vascular cell adhesion molecule-1 (VCAM-1), and CD34, but not E-selectin, P-selectin, CD36, CD13, CD44, HLA-DR or PECAM. Upregulation of ICAM-1, VCAM-1, and CD34 was apparent 12 hours after infection and persisted for weeks after infection. Selective induction of adhesion molecules was mediated by the presence of the E4 gene in the Advector, because infection of ECs with an E1(-)E4(-) Advector had no effect on adhesion molecule expression. ECs infected with E1(-)E4(+) Advector, but not those infected with E1(-)E4(-) Advector, supported the adhesion of leukocytes. Monoclonal antibodies to ICAM-1 and VCAM-1 inhibited adhesion of leukocytes to E1(-)E4(+)-infected ECS: Infection of the ECs with E1(-)E4(+) Advector, but not E1(-)E4(-) Advector, resulted in downregulation of expression of chemocytokines, including interleukin-8, MCP-1, RANTES, and GM-CSF. Nonetheless, a large number of leukocytes migrated through ECs infected with E1(-)E4(+), but not those infected with E1(-)E4(l-), in response to exogenous chemokines. These results demonstrate that infection of ECs with E1(-)E4(+) Advectors, but not E1(-)E4(-) Advectors, may directly augment inflammatory responses by upregulating expression of adhesion molecules and enhancing migration through Advector-infected ECs and suggest that E1(-)E4(-) Advectors may be a better choice for gene-transfer strategies directed to the ECS:

publication date

  • May 11, 2001

has subject area

  • Adenoviridae
  • Adenovirus E1 Proteins
  • Adenovirus E4 Proteins
  • Antigens, CD34
  • Cell Adhesion
  • Cell Movement
  • Cells, Cultured
  • Chemokines
  • Down-Regulation
  • Endothelium, Vascular
  • Gene Expression Regulation
  • Genetic Vectors
  • Humans
  • Intercellular Adhesion Molecule-1
  • Leukocytes
  • Proteins
  • Receptors, Cell Surface
  • Time Factors
  • Transfection
  • Up-Regulation
  • Vascular Cell Adhesion Molecule-1

Research

keywords

  • Journal Article

Identity

Language

  • eng

PubMed ID

  • 11348999

Additional Document Info

start page

  • 903

end page

  • 910

volume

  • 88

number

  • 9