Differential interleukin-8 and nitric oxide production in epithelial cells induced by mucosally invasive and noninvasive Trypanosoma cruzi trypomastigotes

Infect Immun. 2003 Sep;71(9):5394-7. doi: 10.1128/IAI.71.9.5394-5397.2003.

Abstract

Trypanosoma cruzi metacyclic trypomastigotes (MT), but not blood form trypomastigotes (BFT), are highly mucosally infective. We investigated the abilities of MT and BFT to induce inflammation and/or intracellular killing activity within mucosal epithelia. BFT, but not MT, induced marked increases in interleukin-8, GRO-alpha, MCP-1, and nitric oxide production in HeLa and AGS cells, despite similar infectivities. MT may avoid induction of inflammation as an important biological mechanism facilitating mucosal invasion.

MeSH terms

  • Animals
  • Cell Line
  • Chagas Disease / etiology
  • Chagas Disease / immunology
  • Chemokine CCL2 / biosynthesis
  • Chemokine CXCL1
  • Chemokines / biosynthesis
  • Chemokines, CXC*
  • Chemotactic Factors / biosynthesis
  • HeLa Cells
  • Humans
  • Inflammation Mediators / metabolism
  • Intercellular Signaling Peptides and Proteins / biosynthesis
  • Interleukin-8 / biosynthesis*
  • Interleukin-8 / genetics
  • Mucous Membrane / immunology
  • Mucous Membrane / parasitology
  • Nitric Oxide / biosynthesis*
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Trypanosoma cruzi / growth & development
  • Trypanosoma cruzi / pathogenicity*
  • Trypanosoma cruzi / physiology

Substances

  • CXCL1 protein, human
  • Chemokine CCL2
  • Chemokine CXCL1
  • Chemokines
  • Chemokines, CXC
  • Chemotactic Factors
  • Inflammation Mediators
  • Intercellular Signaling Peptides and Proteins
  • Interleukin-8
  • RNA, Messenger
  • Nitric Oxide