Induction of intercellular adhesion molecule 1 gene expression by measles virus in human umbilical vein endothelial cells

J Med Virol. 1999 Jan;57(1):9-16. doi: 10.1002/(sici)1096-9071(199901)57:1<9::aid-jmv2>3.0.co;2-2.

Abstract

The expression of intercellular adhesion molecule 1 (ICAM-1) by endothelial cells is important for the regulation of adhesion and transendothelial migration of a variety of leukocytes that express the integrins lymphocyte function-associated antigen 1 (LFA-1) and/or Mac-1. Here, we demonstrate strain-specific differences in the ability of measles virus (MV) to induce ICAM-1 expression. The vaccine strain Moraten (Mor) rapidly induced high levels of ICAM-1 mRNA and protein expression, whereas the vaccine strain CAM-70 and the Edmonston wild type (Ed-wt) strain were far less effective, even when they were used at very high multiplicities of infection (MOIs). Strain-specific differences in the induction were not a consequence of differences in the ability to infect ECs. Furthermore, induction of ICAM-1 by Mor was not dependent on de novo expression of MV or cellular proteins. Dual-immunofluorescence analysis indicated that there was no association between the expression of either MV nucleocapsid or hemagglutinin protein and the induction of ICAM-1 expression. Some human umbilical vein endothelial cells (HUVECs) that expressed high nucleocapsid protein in response to either Mor or CAM-70 failed to express elevated ICAM-1, whereas some HUVECs that were incubated with Mor expressed high ICAM-1 prior to expression of MV nucleocapsid protein. Strain-specific differences in the ability of Mor and CAM-70 to induce ICAM-1 correlated with their ability to activate the latent transcription factor NF-kappaB. These studies suggest a preexisting component of MV particles that leads to strain-specific differences in the activation of NF-kappaB and the induction of ICAM-1 gene expression.

Publication types

  • Comparative Study
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Blotting, Northern
  • Chlorocebus aethiops
  • Endothelium, Vascular / cytology
  • Endothelium, Vascular / metabolism*
  • Enzyme-Linked Immunosorbent Assay
  • Epithelial Cells / metabolism
  • Epithelial Cells / virology
  • Fluorescent Antibody Technique
  • Hemagglutinins, Viral / metabolism
  • Humans
  • Intercellular Adhesion Molecule-1 / metabolism*
  • Measles virus / growth & development
  • Measles virus / metabolism*
  • Membrane Glycoproteins / analysis
  • Membrane Glycoproteins / metabolism
  • NF-kappa B / metabolism
  • Nucleocapsid Proteins / metabolism
  • RNA, Messenger / metabolism
  • Umbilical Veins / cytology
  • Umbilical Veins / metabolism*
  • Vero Cells
  • Viral Proteins / metabolism
  • Viral Vaccines / pharmacology

Substances

  • Hemagglutinins, Viral
  • Membrane Glycoproteins
  • NF-kappa B
  • Nucleocapsid Proteins
  • RNA, Messenger
  • Viral Proteins
  • Viral Vaccines
  • Intercellular Adhesion Molecule-1