Destruction of human microvascular endothelial cell capillary-like microtubules by Brazilian purpuric fever-associated Haemophilus influenzae biogroup aegyptius

Pathobiology. 1994;62(2):109-12. doi: 10.1159/000163886.

Abstract

When grown in the presence of Matrigel, monolayers of an immortalized human microvascular cell line (HMEC-1) form capillary-like microtubule networks. Previous work, using HMEC-1 monolayers, demonstrated a significant difference in in vitro cytotoxicity between Brazilian purpuric fever (BPF)-associated Haemophilus influenzae biogroup aegyptius (HAE) strains and non-BPF-associated HAE strains. The present study demonstrates that BPF-related cytotoxic differences can also be observed in HMEC-1 microtubule networks. At a multiplicity of infection (MOI) of 2 x 10(-2) bacteria/tissue culture cell, BPF-associated strain F3031 disrupted the microtubule network, producing random clumps of rounded cells at 48 h of incubation. Infection with non-BPF-associated strain F1947 at the same MOI produced no observable microtubule disruption. The ability of HMEC-1 microtubule model to differentiate virulent and avirulent HAE in vitro will further aid in the study of BPF pathogenesis. In addition, the fact that the HMEC-1 cells can be induced to form microtubules make it an excellent model system for the general study of many of the agents of vascular purpura.

Publication types

  • Comparative Study

MeSH terms

  • Bacterial Toxins / toxicity*
  • Cell Death
  • Cell Line
  • Collagen
  • Drug Combinations
  • Endothelium, Vascular / microbiology
  • Endothelium, Vascular / ultrastructure*
  • Haemophilus Infections / microbiology
  • Haemophilus influenzae / isolation & purification
  • Haemophilus influenzae / pathogenicity*
  • Humans
  • Laminin
  • Microtubules / drug effects
  • Microtubules / microbiology
  • Microtubules / ultrastructure*
  • Proteoglycans
  • Purpura / microbiology
  • Virulence

Substances

  • Bacterial Toxins
  • Drug Combinations
  • Laminin
  • Proteoglycans
  • matrigel
  • Collagen